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Cnj - Scientist

Allied Innovative Systems, a NJ based early stage medical technology company, is seeking a Biochemist to join our research team, and participate in transitioning medical research projects into commercial products. Responsibilities include designing and performing experiments, prototyping and documentation. Candidates must have a good understanding and some experience in immunoassay development, ELISA, and DNA analysis. Qualifications: •MS or PhD Degree in Biochemistry, Biophysics, Chemistry •Experience in analytical biochemical assays. •Excellent learner and team player •Experience in optical methods of detection is a plus. The candidate is expected to participate in scientific publications that could help further his/her career goals. Submit your resume to: allinsys@verizon.net

Cnj - Data Analyst for Pharma Co (P356)

This position is responsible for data analysis support of the manufacturing operations. This position will report to a Director, Associate Director, Manager or Supervisor in Manufacturing Technology and will interact with the manufacturing, quality assurance and quality control departments. Knowledge of cell culture, purification and support systems is a plus. Spreadsheet and/or database experience a plus. Responsible for supporting manufacturing operations through the performance of the following duties: 1.Verifies the accuracy of the data entered into the in-process database by the Manufacturing staff and ensuring that all of the data entries are complete. 2.Assists with the trending and analysis of manufacturing production data to support: Non-Conformance Events, process validation protocols and reports, comparability and consistency protocols and reports, technical transfer documentation, BLA filings, annual manufacturing summaries for regulatory documentation, etc. 3.Assists with the maintenance of the manufacturing in-process database. 4.Provides in-process data for technical reports supporting technology transfers, deviation/adverse event reporting and process analysis/trending. 5.Performs all job responsibilities in compliance with current Good Manufacturing Practices. 6.May be asked to support projects in Manufacturing Support & Process Validation Group. 1.BS degree in Chemical Engineering, Microbiology, Biochemistry or Chemistry 2.BS with 1-5 years experience or BSE with 0-3 years experience in a GMP production/development environment. 3.Where applicable, demonstrated superior performance as a Manufacturing Technologist. 4.Experience in fermentation and/or protein purification manufacturing a plus. 5.An understanding of current Good Manufacturing Practices a plus. 6.Strong mathematical and analytical skills. 7.WORD, EXCEL, Powerpoint and VISIO experience a plus. 8.Excellent communication skills, both oral and written. Interested Candidates please email your resume to stephanie.batchelor@expresspersonnel.com and call Stephanie at 908 252 9520 to discuss.

Cnj - Supply Center Associate II

Position Objective: Administers Invitrogen Supply Center locations creating high visibility for Invitrogen throughout the entire account which will result in double digit growth. The balance of time spent is providing customer service in the field and participating in growth-driving activities at both the Supply Centers and overall account: implementing strategic marketing activities, driving Point-Of-Sale (POS) activities, engaging customers, and driving adoption of Invitrogen products through cross-selling, up-selling and conversion. Essential Functions: Supply Center administration (See list of Essential Functions for Supply Center Associate). Drives operating efficiency of Supply Center locations through implementation and use of electronic systems. Post signage for product features, promos or special Marketing initiatives. Able to describe products and promotions to customers. Initially need regular AM guidance as to availability of resources and time, but learn to make independent decisions as to availability of resources and time, learning how to use appropriate internal and external resources as needed. Help AM hit specific growth targets at assigned key account(s) by learning to execute activities such as: Profiling, merchandising, basic demos, SC events, Marketing initiatives/promos, Market and competitive intelligence (QMI), new SC starts, adjusting inventory. Learn to use Siebel, Cognos and other revenue tracking tools. Develop basic knowledge of Invitrogen technology and products in customer workflow areas. Learn to conduct simple product demonstrations and answer basic questions with AM's or TSS's help and guidance, eventually taking part or leading basic demos. Learn about cross-selling and up-selling opportunities and how to execute. Attend planning/strategy meetings with AM and customers around Supply Center and on-site business. Cultivate effective working relationships with internal IVGN personnel and teams. Identify and cultivate effective, dedicated relationships with the key Supply Center account(s). Become recognized as a primary support resource for specific key account(s') on-site retail needs (product selection, ordering, pricing, issues, etc.). Learn to anticipate customer needs, start using internal resources to ensure customer satisfaction and revenue growth. Learn to identify compliance issues and/or opportunities: contracts, purchase commitments, business changes, etc. Learn how to perform Account/Supply Center business reviews. Perform competitive and price audits and drive appropriate responses with AM and Pricing Specialists. Drive adoption of Invitrogen as preferred/primary vendor. Education: A bachelors or equivalent degree required. Degree in life sciences (Molecular Biology or related field) preferred. Experience & Skills: Minimum of 1 year experience in customer interactive environment - sales, support or the like. At least 2 years total work experience required. Experience in a retail environment preferred. Demonstrated proficiency with computers - aptitude with Windows Operating Systems and applications. Access to a home computer and/or laptop with internet access required. Ability to lift objects up to 50-60 lbs. Ability to travel up to 15%. Demonstrated excellent writing, verbal communication and interaction/interpersonal skills. Demonstrated initiative and influence skills. Can accurately relay company positioning. Demonstrated positive attitude and desire to succeed. Learn to bring a high degree of flexibility in adapting to a rapidly changing business environment. Please apply using the link below. https://invitrogen.recruitmax.com/MAIN/careerportal/Job_Profile.cfm?szOrderID=1713&szReturnToSearch=1&szWordsToHighlight=

Centralmich - Adventurous Biologist

Adventurous biologists to observe and sample catches onboard commercial fishing boats off Alaska. Duties include collecting representative samples of the catch, sorting, recording and measuring different species, Requires B.S. in biology or natural sciences, a college level statistics course and a flexible attitude. Strenuous working conditions. Opportunities year around. Training provided. While onboard fishing vessels, biologists identify fish species and collect and record data on the sex, length and quantity for species caught. This fishery data is used by government agencies such as National Marine Fisheries Service (NMFS) and Alaska Department of Fish and Game (ADF&G) to manage commercial fisheries. Requirements: Bachelor's Degree in fisheries science or other biological science, college level statistics course, pass a physical exam, have a minimum of 30 biology credits.Please email your current resume to apply to yani@saltwaterinc.com and visit our website at www.saltwaterinc.com. Questions please call Yani at 907-276-3241.

Chambana - Consulting Ontologist

Ingenuity is a group of creative, energetic and motivated people helping life science researchers understand core biological mechanisms. We deliver systems biology expertise to biologists and bioinformaticists through pathways analysis software, genome-scale computable network datasets, and knowledge management services and infrastructure, resulting in increased R&D productivity and faster drugs to market. We are passionate about our products, and dedicated to providing researchers with the knowledge required to make Better Decisions Faster™. As a Consulting Ontologist you will contribute to building Ingenuity’s Knowledge Base. This position is off-site (work from home), and training is provided. Key Responsibilities: •Research and identify biological concepts from the scientific literature •Represent and connect biological concepts in Ingenuity’s Ontology Education, Experience, and Skills REQUIRED: • BA/BS in a biological discipline (Molecular Biology, immunology, genetics, biochemistry or other related field) •Detail-oriented • Strong logic skills • Internet savvy • Familiar with Microsoft Office tools • Maintain a minimum level of productivity (about 10 hrs/week) Must be legally able to accept consulting work in the US Education, Experience, and Skills DESIRED: •Completion of graduate level coursework is a plus •MS degree, PhD candidacy or PhD degree is desirable •Research experience is a plus

Chambana - Project Engineer

Hexion Specialty Chemicals is the world's largest producer of thermosetting resins. The second-largest North American-based specialty chemicals Company. Hexion generated 2006 sales of $5.2 billion through its leading positions across various end markets and geographies. Our resins are used in bonding, binding and coating applications in a multitude of industries and for virtually thousands of end-use products. Our materials are found in products touching nearly every modern living. Job Objective: Provide long term capital planning process to support Site Mission - reliability manufacture quality products in a safe and environmentally compliant manner to meet business strategies. Essential Functions: Perform preliminary engineering to identify critical project requirements, develop alternatives, conduct cost/benefit analysis to prioritize options, anticipate issues, bottlenecks and roadblocks, develop scope and documents to conduct project reviews, and recommend best options to management. Achieve best return on capital by managing project budget, schedule and performance to meet key performance requirements at the lowest overall manufacturing cost (considering capital, M&R and operating). Perform detailed engineering to develop project scopes/packages that meet critical project requirements, including budget, schedule and performance. Project packages shall support operations, maintainability, constructability, safety and permit reviews. Provide documentation for all engineering and process design, to include equipment and piping drawings, specifications, calculations and analysis, including basis. Understand and meet PSM requirements for engineering and process design. Use MOC process for changes. Understand and meet other regulatory requirements for engineering design, installation and constructions. Provide management with accurate and timely information with which to make justified and appropriate decisions. Make recommendations and await required approval of projects, and spending. Understand regulatory & permit requirements, and obtain required documents in a timely basis by providing necessary information. Obtain required permits for procurement, installation and construction in a timely and efficient manner. Support SMLT contractor management strategy by forecasting workload, provide project design packages for best project controls & change management, communicate and review packages with all stakeholders. Education/Experience - Bachelors Degree in Technical Area (Highly prefer Chemical Engineering) - Ideal candidate will have 5 - 10 years of Project Engineering experience (Highly prefer in Chemical Industry) - Computer skills - Excellent communication both verbal and written - Leadership - Strong Technical Knowledge - Process Safety Management and Process Hazard Analysis To learn more about this and other exciting opportunities with Hexion, visit www.hexion.com to search for jobs and view detailed job descriptions. To Apply for this position, please CLICK HERE

Chambana - Clinical BioPharma Production Supervisor

JOB TITLE:Clinical Production Supervisor 2nd shift FLSA STATUS:Exempt REPORTS TO:Shift Production Manager PRIMARY FUNCTION: Responsible for training, monitoring and supervising clinical production staff. Responsible for employee assignments, safety, quality, production rates, material reconciliation, production reports, timelines and union policies. Department assignments cover blister card packaging, over-encapsulation, bottle filling, pouching operations, clinical labeling, kit assembly, collating and distribution. Responsible for maintaining Class 100,000 clean rooms and controlled substances II through V. SPECIFIC DUTIES, ACTIVITIES, AND RESPONSIBILITIES: •Monitors, organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to GMPs, SOPs, FDA, DEA and OSHA rules and regulations. •Implements procedures to increase productivity and decrease downtime. •Works closely with Clinical Coordinators to establish production needs and requirements for ongoing and future studies. •Oversees both primary and secondary areas equipped with various pharmaceutical packaging equipment including automated bottle line, form, fill and seal, card sealing, labeling and patient kit assembly. •Employee performance evaluations, new employee hiring, disciplinary notices, employee termination, according to company guidelines and performance requirements as established in the union contact. •Develops, reviews and edits related production SOP’s (operational, maintenance, cleaning). •Responsible for maintaining and ordering personnel, safety, disposable and support packaging supplies. •Review and approval of production staff vacation and personal days, along with leave of absence requests. •Responsible for completing batch records in a timely manner. •Investigate and prepare out of specification reports related to production. •Security, accountability and reconciliation of controlled substance in clinical production. •Staging, reconciliation and inventory label generation in JD Edwards. POSITION REQUIREMENTS: •Clinical Trials Supplies experience preferred •Computer literate (Microsoft Word) •Pharmaceutical Packaging and Manufacturing experience •JD Edwards experience or similar ERP systems •Working knowledge of cGMPs, DEA and OSHA rules and regulations •Leadership and team building skills •Demonstrate ability to train, motivate, direct and supervise production personnel •Knowledge of packaging equipment in a Just-in-Time environment •Proven ability to develop Standard Operating Procedures REPORTS TO: Manager of Clinical Operations & Production Manager SUPERVISES: •Hourly Production Personnel EDUCATION: •Bachelor of Science Degree in Health/Chemistry/Pharmacy related field EXPERIENCE OR EQUIVALENT: •5+ years Clinical, contract or production experience

Chambana - "'''Dispatch Supervisor'''"Illinois~~~

Kindler also has said the company plans by 2010 to start introducing two medicines a year that were acquired from other companies. Kindler brought on biotechnology entrepreneur Corey Goodman this month to run a new California-based research center and to scout for new medicines developed outside Pfizer. One possible acquisition may be Cambridge, Massachusetts- based Biogen Idec Inc., the world's biggest maker of multiple sclerosis drugs, analysts said. Billionaire investor Carl Icahn, who made a takeover bid for the company last week, said it may be an attractive target for a pharmaceutical maker in need of new treatments.

Charleston - Clinical Trial Manager

Primary Objective of Position: Plans and manages clinical development trials. Oversees internal and external staff for the timely and quality implementation of trials. Oversees the activities of CROs. Coordinates the training of clinical and other staff. Prepares reports on clinical trials. Performs performance appraisals on direct reports. Major Duties and Responsibilities: - Prepares clinical protocols and amendments. - Oversees or performs feasibility assessment for new clinical protocols. - Identifies, recruits and approves clinical investigators. - Ensures compliance with policies and procedures. - Approves sample, investigator-prepared and IRB-approved informed consents. - Approves or write monitoring plans. - Approves the design, format and content of CRFs, study guides and subject instructions. - Oversees activities associated with clinical site start-up and ensure the collection and maintenance of essential documents. - Ensures appropriateness of forecast for investigational product. - Coordinates the preparation of study budgets. - Manages Investigator Meetings. - Manages the overall Investigational product accountability and reconciliation process. - Ensures that that CRF data queries are resolved. - Oversees and monitors work done by CROs, central labs and other vendors chosen for clinical development activities ensuring delivery against contract. - Provides study-specific outsourcing specifications for RFPs. - Ensures training of clinical staff. - Develops and administer study and project budgets. - Resolves patient eligibility and protocol deviation issues. - Assists in preparation Clinical Study Reports, Annual IND safety reports and clinical. - May monitor clinical sites for adherence to protocol and GCP. Minimum Job Qualification: BA/BS in biological sciences or related fields or BSN. Typically 7-8 years related experience in life sciences or medically related field, including 6 years of clinical development experience and previous 1-2 years of management experience. Skills and Abilities: - Knowledge of relevant therapeutic or product area - Ability to use scientific and clinical knowledge to conceptualize study designs. - Ability to evaluate scientific and clinical strategies for clinical development in a specified product area. - Detailed knowledge of regulations and guidelines ' - Ability to anticipate and resolve problems. - Ability to write and present clearly especially on scientific and clinical issues ' - Ability to work effectively in a team/matrix environment. - Excellent interpersonal, organizational, supervisory and project planning skills. - Proficiency in the preparation and review of clinical sections of study reports and BLA/NDA. - Demonstrated professional collaboration skills. - Experience in all phases of drug development, including international trials. *** Please state hourly wage requirements***

Charleston - Regional Clinical Research Associate I/II

This is a home based regional Clinical Research Associate position. For this position you must have been with a pharmaceutical/Clinical Research Organization for at least six months. This must have clinical research associate experience. You must have independent monitoring experience. I will consider any therapeutic area. You must be within an hour of a major airport.

Charleston - Laboratory Supplies & Chemical Sales

Expanding our sales force and looking for experienced laboratory and chemical sales representatives. We are a rapidly growing eleven-year-old scientific supply distribution company doing business with today’s technology with the “good old boy” approach. We are flexible to meet customer needs. We distribute the widest range of laboratory supplies and chemicals and can meet all our customer needs. This is a commission only position with no cap on what you can make. The representative will carve out their own territory based on familiarity to customers and relationships developed. This position is for a fulltime rep or we invite anyone experienced in the industry looking to supplement his or her income as an optional opportunity. Qualifications will require previous sales experience in laboratory, scientific, chemical or related industries. Send your resume and the area you reside in to labrep@yahoo.com.

Charleston - Vet Technician

Looking for a tech with 3-4 years experience with ability to read fecals, draw blood, give vax and work with little to no supervision. Please send resume with references.

Charleston - Phlebotomist

Life Therapeutics is setting the standard in specialty therapeutic and diagnostic products for the life science market. Life Sera, a division of Life Therapeutics, currently has a position open for a Phlebotomist in our Charleston Donor Center. The Phlebotomist will: Complete donor screening process. Determine donor suitability. Review charts for accuracy and completeness. Draw samples as required. Participate in, and complete donor room tasks. Perform plasmapheresis and whole blood procedures. Complete plasma processing room tasks. Weigh and record product volumes. Draw samples for various testing, assay and customer needs. Document all plasma and serum handling activities. Assist in preparation of plasma shipments if needed. As assigned, perform Quality control on various laboratory equipment. Perform all duties listed above in accordance with DCOP, FDA, CLIA, GHA, and IQPP requirements. • Maintain donor confidentiality. Other duties as assigned. Benefits: We offer competitive compensation and benefits including medical, dental, vision, FSA, company paid basic life insurance and 401K. EOE For immediate consideration, please CLICK HERE or visit www.life-therapeutics.com to apply.

Charlestonwv - Clinical Production Supervisor, Global Leader

PRIMARY FUNCTION: Responsible for training, monitoring and supervising clinical production staff. Responsible for employee assignments, safety, quality, production rates, material reconciliation, production reports, timelines and union policies. Department assignments cover blister card packaging, over-encapsulation, bottle filling, pouching operations, clinical labeling, kit assembly, collating and distribution. Responsible for maintaining Class 100,000 clean rooms and controlled substances II through V. SPECIFIC DUTIES, ACTIVITIES, AND RESPONSIBILITIES: •Monitors, organizes and performs all functions associated with packaging of clinical trial supplies and assures compliance to GMPs, SOPs, FDA, DEA and OSHA rules and regulations. •Implements procedures to increase productivity and decrease downtime. •Works closely with Clinical Coordinators to establish production needs and requirements for ongoing and future studies. •Oversees both primary and secondary areas equipped with various pharmaceutical packaging equipment including automated bottle line, form, fill and seal, card sealing, labeling and patient kit assembly. •Employee performance evaluations, new employee hiring, disciplinary notices, employee termination, according to company guidelines and performance requirements as established in the union contact. •Develops, reviews and edits related production SOP’s (operational, maintenance, cleaning). •Responsible for maintaining and ordering personnel, safety, disposable and support packaging supplies. •Review and approval of production staff vacation and personal days, along with leave of absence requests. •Responsible for completing batch records in a timely manner. •Investigate and prepare out of specification reports related to production. •Security, accountability and reconciliation of controlled substance in clinical production. •Staging, reconciliation and inventory label generation in JD Edwards. POSITION REQUIREMENTS: •Clinical Trials Supplies experience preferred •Computer literate (Microsoft Word) •Pharmaceutical Packaging and Manufacturing experience •JD Edwards experience or similar ERP systems •Working knowledge of cGMPs, DEA and OSHA rules and regulations •Leadership and team building skills •Demonstrate ability to train, motivate, direct and supervise production personnel •Knowledge of packaging equipment in a Just-in-Time environment •Proven ability to develop Standard Operating Procedures REPORTS TO: Manager of Clinical Operations & Production Manager SUPERVISES: •Hourly Production Personnel EDUCATION: •Bachelor of Science Degree in Health/Chemistry/Pharmacy related field EXPERIENCE OR EQUIVALENT: •5+ years Clinical, contract or production experience

Charlottesville - Part time Horticulture Activity Specialist wanted at JABA

•Participate in and communicate activity assessment/plan for each member with ADHC staff and caregivers. Monitor and evaluate member performance. Document findings and recommendations and share with the team; •Provide physical and social enrichment to the members of the Center. Maintain facility-wide safety and security. Provide a safe, healthy, neat, clean and pleasant environment; •When planning field trips, confer with RN or Center Manager to determine which members should participate in a scheduled field trip; •Be alert for, and report any changes in members' physical, mental or functional status (preferably in writing) to RN or Center Manager; •Relay, in writing, any information received from families, or other caregivers, regarding members’ condition, medications, needs or schedule to RN or Center Manager; •Provide training and supervision to Program Assistants and CNAs for tasks related to horticulture activities; and provide and participate in regular in-service programs; •Maintain activity equipment and supplies. Advise Center Manager of the need for additional/replacement equipment and supplies. Upon approval, order, inventory and store items. Inventory equipment and supplies after each activity; •Maintain a file of community service groups and individuals who may contribute to the horticulture activity program at the Center; •Identify and contact businesses who may donate goods or services. Record donations; coordinate with Development Office regarding acknowledgement of donated items, and send thank-you letters; •Update and improve skills/knowledge. Participate in staff meetings by presenting in-service topics and suggestions. Attend workshops and trainings where appropriate and approved by the Center Manager; •Coordinate with other horticulture groups. Solicit written materials or advice from other sources to increase level of services at the center; •Keep informed of and follow Center policies and procedures; •Contribute to success of ADHC program by developing improved public relationships, networking with other organizations and enhancing the professional performance of the position; •Maintain appropriate, professional standards of personal grooming, dress and behavior. •Desired though optional--Become certified through JAUNT to drive buses for special trips which may be planned for the members. •Participate in JABA/JEC Employee Evaluation and Support Program review with his/her supervisor; •Perform other appropriate functions assigned by the Center Manager. •Horticulture Activity Work with staff and volunteers to plan and implement Horticulture Activity groups with members, including: intergenerational programming; one-on-one work with identified members; outings with members; speakers; attendance at weekly staff meetings; attendance at care plan meetings; meeting with Center Manager as needed; purchase of tools and supplies; assistance with budget planning; and assistance seeking funds for program support. •Greenhouse Operations Keep the greenhouse orderly and functioning; order supplies; water; weed; coordinate volunteers; conduct plant sales; coordinate with other agencies; monitor budget; keep Center Manager informed of special events. •Landscape Order plants, materials, and supplies; install plants; weed; water as necessary; prune, mulch, and compost as necessary and coordinate The ideal candidate must have a bachelors degree in related field, e.g. nursing, geriatrics, horticulture, agriculture, landscape architecture, etc.; •Knowledge of plants and gardens, the human aging process, and good communication skills; •1 year experience working with the elderly or persons with disabilities; •Current CPR and First Aid Certification; •Physical capacity necessary for manual labor (to lift up to 50#) and to assist and support members;

Charlottesville - Program Manager, Reimbursement

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com. Job Description - External: The primary day-to-day client contact for existing projects. Oversee staff activities and performance. Provide management, administration and leadership to ensure that projects proceed on time and within designated budget. Responsibilities: ' Supervise Staff ' Provide leadership, coaching, mentoring, feedback and role modeling to team members to assure quality, accuracy and completeness of deliverables ' Communicate to team members the scope of work, timelines and program/project goals, technical information, deliverables, and input from client throughout the duration of the program/project ' Inform team members of any new information or modification of program/project related issues that may affect specific responsibilities of team members ' Schedule activities and deliverables, including timelines, for staff ' Facilitate communication within the team through team meetings, e-mails and monitor engagement/morale of team members. ' Provide or arrange for program/project-related training as needed for team members ' Resource planning and management. Track resources and actual time spent for project tasks for all team members ' Adhere to program SOPs and metrics ' Serve as primary client contact for day-to-day program activity ' Respond to day-to-day client inquiries associated with specific programs/projects ' Manage client expectations ' Prepare and provide activity reports for the client ' Coordinate operational activities of program/project from initiation to completion ' Write program SOPs, guidelines, client deliverables (e.g. reports, memos, etc.) ' Ensure that appropriate review and approval of project-related documents and correspondence occurs ' Understand billing and coding procedures for program products ' Assure appropriate monthly revenue is recognized for all assigned projects ' Submit monthly resource/activity reports to Associate Director/Director ' Calculate monthly revenues recognized for the program/project and submit monthly updated forecasts for revenue recognition and invoicing to the Associate Director ' Assume responsibility for all tasks which are not otherwise delegated ' Conduct performance reviews ' Understand reimbursement and patient assistance strategy and program design for pharmaceutical products ' Identify new opportunities within client account and collaborates with Associate Directors ' Support organization vision and values and ensures team activities are aligned accordingly ' Prepare and conduct client presentations/trainings as necessary ' Travel as required ' Perform other tasks as assigned by management Experience - External: Education: Bachelor's degree Minimum Work Experience Requirements: Minimum of 3 - 5 years in health-related field with minimum 2 years of managing people and projects. Special Skills/Knowledge: Moderate level consulting skills. Thorough working knowledge of organization's service offerings and processes. Keeps current on body of knowledge within area of responsibility. Understanding of the pharmaceutical, biotechnology, medical device or other healthcare industries. Demonstrated leadership skills that include the ability to gain trust and confidence with a variety of personnel and clients. Strong interpersonal and negotiation skills; excellent decision-making skills and strong analytical skills; must be well organized and show attention to detail; must understand complex organizational relationships; take a proactive approach in dealing with project problems/issues; strong oral and written communication skills; strong computer skills. excellent customer service skills; travel as necessary; presentation skills, motivated to work consistently in a fast-paced and rapidly changing environment. Please contact: Dorothy Hughes Dorothy.Hughes@kenexa.com

Chicago - Manager Regulatory Affairs

Follow your aspirations to Abbott for diverse opportunities, competitive salaries, great benefits, a 401(k) retirement savings plan, a company paid pension plan and profit sharing, all with a company providing the growth and strength to build your future. Description: The Manager, Regulatory Affairs identifies and obtains data needed and ensures they are effectively presented for submissions to FDA. Manages regulatory submission and approval process, including assuring complete and timely response to FDA during application review. Serve as liaison with FDA for routine communications in support of filings and interface with FDA for meetings, teleconferences, etc. Manages all submission-related activities for assigned projects. Assesses R & D and marketed product programs against US-specific requirements and provides strategic input. Develops and/or provides input into the regulatory and promotion strategy for on-market products. Works largely independently. Uses tact, persuasion, and negotiation skills to effectively lead cross-functional groups in the completion of tasks and projects. Qualifications: 5-7 years in Regulatory, R&D, or related area with minimum 3 years in Regulatory. Education: Bachelor Degree in Pharmacy, Biology, Chemistry, Pharmacology or related subject. Abbott welcomes and encourages diversity in our workforce. EEO/AATo apply for this position, please visit us at: http://appclix.postmasterlx.com/track.html?pid=402881bd165bdef901165dcf1368046c&source=craigslistchicago&p=codes=CRL

Chicago - Entry Level Field Chemist

ENVIRONMENTAL FIELD CHEMISTS: As a Lab Pack Chemist you will be responsible for handling, packing, transportation and disposal of hazardous laboratory chemicals and wastes, while adhering to environmental regulations. You will assist customers with laboratory moves and facility closures. In conjunction with local community officials, you will participate in Household Hazardous Waste Days collecting and preparing for disposal residential hazardous waste. You will experience a wide variety of field sites and be responsible for building superior customer service through professionalism, safety, and innovative solutions. This is a blue-collar chemist position not a research and development or a lab position. A Degree in Chemistry/Environmental Science or equivalent experience is preferred. The successful candidate will have superior communication and the desire for advancement. Must have the ability to obtain a Commercial Drivers License after six months in position. Occasional overnight travel is possible. Clean Harbors, Inc. is North America's leading provider of environmental and hazardous waste management services. With an unmatched infrastructure of 48 waste management facilities, including nine landfills, five incineration locations and seven wastewater treatment centers, the Company provides essential services to more than 45,000 customers, comprising of more than 175 Fortune 500 companies, thousands of smaller private entities and numerous governmental agencies. Headquartered in Norwell, Massachusetts, Clean Harbors has more than 100 locations strategically positioned throughout North America in 36 U.S. states, six Canadian provinces, Mexico and Puerto Rico. We offer competitive salaries and progressive benefits including health, dental, life insurance, 401K, Employee Stock Program, generous paid time off, tuition reimbursement and more. We offer a drug free work environment and require a pre-employment drug screen. All Applicants are subject to pre-employment security background checks, and some positions may require pre-employment physical fitness for duty tests Clean Harbors is looking for talented individuals to join our team. Please fax your resume to 781-792-5902 or e-mail to: Jane Shamaly – shamaly.jane@cleanharbors.com Clean Harbors is an Equal Opportunity Employer

Chico - Field Project Implementation Manager - Municipal Wastewater & Water

Field Project Implementation Manager-Wastewater & Water Facilities ****Please Tell Your Friend/Associates About This Position!**** -Top Pay, Outstanding Working Environment for Great Talent- Field Project Implementation Manager - Municipal Wastewater & Fresh Water Facilities Talented, Self-Motivated Help Wanted for Field Project Implementation Manager Wastewater/Fresh Water Facilities Upgrade Implementation Please Send Resume and Cover Letter to: HR.ProjectManagement@gmail.com Start Date: ASAP Salary range: $50k - $75+k/year, DOE - Outstanding Benefits! Leading Seattle-based west coast engineering firm has an immediate opening for a dynamic, resourceful Field Project Implementation Manager for municipal wastewater and fresh water facilities upgrade projects. This position requires a thorough knowledge of the principles and practices associated with PLC/SCADA/electrical/mechanical elements in municipal/district public works wastewater and or fresh water systems related to system process controls. This is an outstanding position for a detail-oriented, resourceful self-starter with good people skills. There is excellent opportunity for growth and advancement for someone with a "get it done" mindset. Sense of humor is a must. Responsibilities: • Work with the in-house engineering team to develop and implement wastewater and freshwater upgrade projects. • Manage site work done by vendors and contractors, ensuring the highest standards of quality and service are met or exceeded, • Work with vendors and contractors regarding bids, schedules and budgets • Maintain up-to-date and complete project records, track project timetables to ensure expedient, high quality implementations • Assist with implementation "on the ground.” Understand process electrical, mechanical, PLC and SCADA systems. Adept problem-solving abilities to meet challenges as they arise. • Attend internal and external project development and implementation meetings as required. • Maintain excellent working relationships with municipal/district management and staff. • Reports directly to company ownership/senior management. • Average two weeks per month regional travel devoted to contract sites to oversee and assist with project implementations. Qualifications: • Knowledge of current municipal/district wastewater and or freshwater practices and processes, as well as insight into challenges arising as upgrades are required. • Experience effectively working with municipal/public works management and staff. • Experience in project budgeting, scheduling and implementing municipal water projects. • Experience in working with/overseeing subcontractors and vendors. • Excellent written and oral communication skills. • Knowledge and use of MS Office software. • Solid experience with wastewater/ fresh water processes, control logic, PLC programming, and industrial automation in general, is highly desirable. While not necessary, engineering, project management or equivalent project experience in a municipal or public works setting is a plus. • Valid driver's license, good driving record, insurance. Salary is DOE and VERY strong compensation package includes: medical, dental, paid vacation, 401K. Please forward your resume, cover letter and job goals via e-mail to: HR.ProjectManagement@gmail.com -Seattle Waterfront Offices - Beautiful Setting

Chico - MAINTENANCE TECHNICIAN

Local company has a full time position open for a maintenance and operation technician to work on private wastewater treatment systems. This is an interesting and expanding occupational field, which integrates aspects of mechanics, plumbing, biology, soils, hydrology, enigineering and ecology. Preference will be given to applicants familiar with STEP systems, intermittent sand filters, bottomless sand filters, and Advantex Pod systems. Also helpful is a working knowledge of bio-tube filters, clarifiers, pumps and vaults; possibly someone with a Class 1 Operator's license. Minimum requirements for a trainee would be: plumbing, mechanical and electrical skills. Needs to be a self-starter with good problem solving skills. Must also have physical strength and endurance to perform certain maintenance tasks at plant sites. This position requires some on-call nights and weekends. All applicants must be flexible, punctual, and have the ability to multi-task in a demanding work environment. Employees are expected to be ethical, moral, and to represent the company with the highest standards possible. We offer competitive wages and benefits, as well as on-the-job training. Drug testing is required. Please send your resume for consideration to: Boxholder P.O. Box 7908 Chico, CA 95927 or FAX to: 530-343-4222

Cincinnati - Adventurous Biologist

Adventurous biologists to observe and sample catches onboard commercial fishing boats off Alaska. Duties include collecting representative samples of the catch, sorting, recording and measuring different species, Requires B.S. in biology or natural sciences, a college level statistics course and a flexible attitude. Strenuous working conditions. Opportunities year around. Training provided. While onboard fishing vessels, biologists identify fish species and collect and record data on the sex, length and quantity for species caught. This fishery data is used by government agencies such as National Marine Fisheries Service (NMFS) and Alaska Department of Fish and Game (ADF&G) to manage commercial fisheries. Requirements: Bachelor's Degree in fisheries science or other biological science, college level statistics course, pass a physical exam, have a minimum of 30 biology credits.Please email your current resume to apply to yani@saltwaterinc.com and visit our website at www.saltwaterinc.com. Questions please call Yani at 907-276-3241.

Cincinnati - Food Technologist

Research and Development Food Techologist *B.S. degree in a Science related field *Must have at least 2 years of R & D experience with further processed poultry products *Bench top formulation *Company will pay relocation expenses

Cincinnati - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Cincinnati - Sales Representative

What We Do Brinkmann Instruments, Inc. is the US regional office of world-renown Metrohm AG (Herisau, Switzerland), an industry leader in laboratory instruments and accessories for titration and electrochemistry research. Located in Westbury, (central) Long Island, New York, we are responsible for supporting all US and Canada sales, marketing, service and distribution activities. In addition to Metrohm products, our Sales and Marketing teams also represent equally renowned manufacturers, including Lauda, KINEMATICA and others, of high quality tools and equipment for chemical and industrial research and testing. Our innovative, high quality products are found in laboratories of all kinds—academic, industrial, research, quality control, processing, manufacturing and scale-up—and all are designed to help meet practical, scientific and economic goals. Brinkmann companies in North America include Brinkmann Instruments, Inc., in the US and Brinkmann Instruments Canada Corp. in Canada. As part of a global company and growing entity you will be part of a progressive and high-energy team, focused on bringing quality products to market and excelling in quality customer service. We are an Equal Opportunity Employer, offering competitive salaries and an attractive health and benefits package. Sales Representative Job Description * Travels throughout Kentucky, Ohio and Indiana to create demand for the company's products * Demonstrates product samples to end user customers * Trains distributor personnel on proper function and usage of selected Brinkmann products * Attends trade exhibits for the purpose of promoting products * Maintains company customer files in current database Skills and Education * Bachelor's degree (B.S.) from a four-year college or university; and one to two years' related sales experience and/or training, or equivalent combination of education and experience * Chemistry background required * Must be computer literate and a self-starter with excellent communication skills Why Work for Us? You will be working in a professional, corporate environment. In return for your contributions, you will receive a competitive salary and an excellent company paid benefits package. A sampling of our company paid benefits include: * comprehensive medical * comprehensive dental * basic life insurance * accidental death and dismemberment * short and long term disability * tuition reimbursement program * paid vacation * paid holidays * paid sick and personal days * 401k plan * profit sharing plan * plus more! This position includes a company car and a complete sales technical package – laptop, Blackberry, etc. Brinkmann Instruments, Inc. is an equal opportunity employer. M/F/V/H

Cincinnati - Research Associate

We are a biopharmaceutical company that is developing products that are delivered directly to the site of tissue injury, preemptively inhibiting inflammation, pain and other problems associated with medical and surgical procedures. Our products are designed to act on distinct molecular targets at the site of delivery, providing improved therapeutic benefit while minimizing the risk of side effects. We are working on a pipeline of products for use in orthopedics, urology, cardiovascular medicine, general surgery and pain management. Benefits of working for us include pre-IPO stock options and competitive salary. Responsibilities: • Perform routine site visits, including pre-study, initiation, interim and closeout visits. Performs responsibilities with minimal support from management. Visits to include monitoring of proper informed consent procedures, compliance with protocol, GCP/ICH Guidelines and other applicable regulatory requirements, and assurance of good site performance. This is accomplished by detailed review of subject records, essential documents, investigational product disposition and accountability, site personnel and procedures. • Manage assigned sites by regular contacts to ensure site compliance, adequate enrollment, and understanding of study requirements. • Report to project team and site personnel any findings noted at monitoring visits. This is accomplished by completion of monitoring reports and follow-up letters within the project-specific timelines. Significant issues noted must be reported to appropriate personnel immediately. • Maintain project tracking system of subject and site information. • Participate in company-required training programs. • Perform necessary administrative functions (e.g., tracking of expense reports, time and attendance). Qualifications • Bachelor's level degree in life sciences, pharmacy, nursing or RN preferred • 2+ years clinical monitoring experience, including field monitoring, site and study start up and management, experience in drug/device development • In-depth Knowledge of Good Clinical Practices (GCP's), ICH Guidelines, FDA regulations and other applicable regulatory requirements • Strong leadership skills • Ability to work independently in a fast-paced environment • Strong communication, interpersonal, and organizational skills • Must demonstrate good computer skills • Position requires approximately 60% travel (may be up to 80% during peak times) Required Skills -------------------------------------------------------------------------------- Clinical Research Associate, Biopharmaceutical, GCP Good Clinical Practices, ICH, Monitoring If you are a good fit for the Midwest Regional Clinical Research Associate - Biopharma position, and have a background that includes: Clinical Research Associate, Biopharmaceutical, GCP Good Clinical Practices, ICH, Monitoring and you are interested in working the following job types: Biotech, Pharmaceutical, Healthcare Within the following industries: Pharmaceutical, Biotechnology, Real Estate - Property Mgt Our privacy policy: Your resume and information will be kept completely confidential. Looking forward to receiving your resume through our website and going over the job in more detail with you! Apply online by reviewing the job listing at: http://www.bioemployment.com

Cincinnati - Microbiology Technician

Science Job Classification: Contract Description:Microbiology TechnicianThe technician for this position will be performing basic micro work such as media prep, plating, streaking, pipetting, and cell counting on a daily basis. These tests will be performed on raw in-process and finished products.The ideal candidate will have a BS in Microbiology or Biology with 6 months to 3 years of experience. This is a first shift position Monday through Friday.CompetenciesDesired:PLATING, STREAKING, CELL COUNTING Contact Information Contact: Fields,Jennifer L

Cincinnati - Data Analyst

Classification: Full Time Compensation: $45000 to $55000 per year A well respected Cincinnati based company is actively seeking a Data Analyst to join their team. The Data Analyst will develop, maintain and enhance mechanisms to track, trend, and report quality measures to support the continuous quality improvement process needs of the Quality Department through comprehensive analysis and documentation of data pertaining to company performance goals. The Data Analyst will compile and analyze data including comparison of outcome measures to benchmark, identify trends, complete barrier analysis, and assist in the identification of activities to reach performance goals. Job Requirements JOB REQUIREMENTS: Education and Experience: • Bachelor's degree in business, science, healthcare or related field preferred. Equivalent experience considered. • 2+ years data analysis or statistical experience. • Proficient with window based environment, particularly Microsoft Excel and Access. Working knowledge of information systems including database design and SQL. • Previous HMO/Managed Care industry experience preferred. • Knowledge of SPSS preferred. • Understanding of ICD-9 and CPT coding system helpful. • Excellent analytic skills, attention to detail. • Detailed familiarity with computer systems, word processing, spreadsheet, statistical packages and other data base management software. • Good organizational skills; the ability to handle multiple priorities simultaneously with a high quality result. • Excellent writing skills. • Appreciation of cultural diversity towards target population

Cincinnati - Regional Clinical Research Associate I/II

Regional Clinical Research Associate I/II Job Description: The responsibility of the CRA I/II is to oversee the conduct of a Pharmaceutical clinical trial to insure the quality and integrity of data and safety and efficacy of the drug. In coordination with the team leader, exercise responsibility for project activities related to monitoring function. Interface with clinical investigators and other site personnel in order to carry out this responsibility. Required Experience: •Education: RN, relevant clinical experience or 4 year Life Science degree. •Minimum Work Requirements: 6 months of clinical drug trial field monitoring experience with a pharmaceutical, CRO, or device company for CRA I. For CRA II you must have at least 2 years experience. •All Therapeutical areas will be considered. You will go to the front of the line if you have Oncology, Cardiovasculor or HIV experience. •Skills: Ability to communicate with professional medical personnel. Understanding of the drug development process. Ability to complete tasks in an accurate and timely manner. •Physical Requirements: Ability to travel an average of 75% and be within one hour of a major airport. Other information: This position is with a large Clinical Research Organization (CRO). It is a home based position. You must have the required experience noted above. Please do not email me your CV if you are a lab tech, foreign MD or someone who “knows they can do the job”. I am sure you all are great people but I need experienced monitors.

Cincinnati - Exciting Project Opportunity - Human Resource Specialist

Classification: Full Time Compensation: $25000 to $35000 per year Job Requirements 2 Years Human Resource experience with at least one year focused on Recruitment. Two or four year degree required. Systems & Software: Microsoft Word, Excel, Powerpoint, SAP HR, Peoplesoft and/or Oracle. Interested candidates must be willing to commute to client locations everywhere in Greater Cincinnati (275 loop & surrounding areas.)

Cincinnati - Geologist

Engineering Job Classification: Contract Description:A national environmental/geotechnical and engineering firm is looking for a Staff Geologist to move into a Project Management role in the Cincinnati area. Requirements0-3ye ars experience, duties may include planning and implementing field investigations (preparation of work plans, coordination with oversight of subcontractors, logging of boreholes and construction of monitoring wells, environmental sampling, record keeping, analyzing and interpreting geologic, hydrologic and analytical reports.CompetenciesDesired:GEOLOGIST, GEOLOGIST PHASE I, ENVIRONMENTAL FIELD SAMPLING, GEOTECHNICAL DRILLING, RETAIL PETROLEUM, UNDERGROUND STORAGE TANK Contact Information Contact: Brewer,Sean P

Cincinnati - QC Microbiologist

Science Job Classification: Contract Description:QC MicrobiologistThese microbiologists will be performing environmental monitoring, particulate, bio burden, and utilities sampling testing on a regular basis. These candidates will be applying GMP's and SOP's in conjunction with FDA regulations.CompetenciesDesired:plating, streaking, cell culturing Contact Information Contact: O'Keefe,Kevin

Cincinnati - Manufacturing Line Mechanic

Biotech Job Classification: Contract Description:We are looking for a manufacturing line mechanic for a large pharmaceutical company in the Cincinnati area.The qualified candidate will have 1 + years experience with a strong mechanical aptitude. Department experience and APAC's knowledge is desirable. This is a full time, 2nd shift position. The candidate for this position will have a High School Diploma or GED. CompetenciesDesired:MECHANICAL APTITUDE, Troubleshooting Machinery, INVENTORY, maintenance Contact Information Contact: Martino,Gillian Stage

Cincinnati - Quality Lab Technician

Science Job Classification: Contract Description:Quality Lab TechnicianWe are currently looking to fill openings covering a wide variety of experience. Qualified candidates should have a B.S. degree in Biology, Chemistry or a related scientific discipline. On a daily basis, these lab technicians will perform quality testing on raw in-process and finished materials. Lab Technicians will utilize HPLC,GC, and wet chemistry techniques to perform these tests.CompetenciesDesired:WET CHEMISTRY, HPLC, GC, Quality Documentation Contact Information Contact: Fields,Jennifer L

Cincinnati - Project Manager - Web Development

Classification: Contract to Full Time Compensation: $67000 to $82000 per year Responsible for the coordination and completion of web projects. Reviews, analyzes, and evaluates business systems and user needs Formulates systems to parallel overall business strategies Writes detailed description of project specification documents, such as business requirements, program functional specifications, and technical design documents Documents detailed steps required to develop or modify systems Provides oversight for system testing, support and quality assurance Writes detailed use case scenarios Set and manage end user expectations. All applicants applying for U.S. job openings must be authorized to work in the United States. All applicants applying for Canadian job openings must be authorized to work in Canada. Job Requirements Familiarity with Internet solutions and relational database concepts Familiarity and basic understanding of HTML coding and scripting technologies, web based applications, flash, SQL Server, Javascript, XML, C#.NET and ASP.Net. PMP preferred.

Cincinnati - Quality Administrator - Medical Devices

JOB SUMMARY: The Quality Administrator is responsible for ensuring the Company Quality System is in compliance with domestic and international medical device quality system regulations. The Quality Administrator is the lead person for the AtriCure organization to refer daily quality questions to. In the role of the Quality Administrator, this person will work with the entire organization to ensure compliance with the Quality System and will be responsible to report to management issues revolving around quality system compliance PRIMARY ROLES AND RESPONSIBILITIES: 1.Authorized to make changes for improvement to the Quality System. 2.Responsible for inspection/testing for quality and products as assigned. 3.Responsible for managing and reporting on Customer Complaints and MDRs in the quality system. 4.Responsible for audit activities for the Internal Audit program and external audit activities. 5.Responsible for processing Document Change Notices through the quality system. 6.Responsible for processing Datat Control Protocols and Reports through the quality system. 7.Responsible for the Quality System Records filing and maintenance of the files 8.Responsible for record retention of Quality System Records 9.Responsible for training employees to the company Quality System 10.Responsible for understanding domestic and international medical device quality system regulations 11.Provides support for preparation and presentation materials for Management review 12.Responsible for compliance to Company Quality System and Company policies 13.Provides support for Customer Management Program as required 14.Provides support for Product Development Department as required 15.Performs Quality System activities in addition to the above as assigned by Supervisor 16.Knowledge of Software Data Base Management and standard office programs 17.May have other document control personnel direct reports 18.Provide support for international registrations of medical device products (e.g. EU class IIb and Class III) QUALIFICATIONS/NECESSARY COMPETENCIES: Undergraduate or Equivalent Experience (Financial/Quality) Inspection/auditing Computer/Data Entry Skills Regulatory Experience Statistical Use Experience Written/Report Writing Skills Good Verbal Communication Skills # of Years Experience in Comparable Position2 OTHER QUALIFICATIONS/NECESSARY COMPETENCIES AS NEEDED: 1.Strong organizational and time-management skills 2.Ability to present training in individual and group setting 3.Experience in FDA regulated company is desired. LICENSES/CERTIFICATIONS DESIRED: 1.ASQ Certified Quality Technician 2.ASQ Certified Quality Auditor 3.ARMA International Certified Records Manager (CRM). 4.Software Validation / Protocol Development

Cincinnati - Laboratory Technician

Science Job Classification: Direct Hire Description:Qualified candidates will be working in a laboratory utilizing GC, FTIR, PH and basic wet chemistry.Ideal Lab Technicians will have 6mos to 2 years. A degree is not requires but experience is a must. Candidate will be trained on all instrumentation and must have a positive attitude and willingness to learn.CompetenciesDesired:GC CHEMISTRY, BENCH WET CHEMISTRY, HPLC Contact Information Contact: Martino,Gillian Stage

Cincinnati - Regional Clinical Research Associate I/II

This is a home based regional Clinical Research Associate position. For this position you must have been with a pharmaceutical/Clinical Research Organization for at least six months. This must have clinical research associate experience. You must have independent monitoring experience. I will consider any therapeutic area. You must be within an hour of a major airport.

Cincinnati - Direct Hire! Data Security Analyst

Classification: Full Time Compensation: $60000 to $70000 per year Job Requirements Knowledge normally acquired through the completion of a Bachelor's degree in Computer Science, plus two to four years of information systems security or data processing auditing related experience. Strong working knowledge of information systems security standards and practices. Solid knowledge of two or more of the following: Microsoft Windows XP, Windows 2003, IIS, SQL Server, and/or UNIX-based OS and networking required with an emphasis on security infrastructure. Must have experience using security information and event management software from vendors such as McAfee/Foundstone, Microsoft, Idera, Ecora, ISS, or Qualys. Candidate must also possess strong written and oral communication skills, strong analytical skills, and attention to detail. Possession of CISSP (Certified Information Systems Security Professional) or CISM (Certified Information Security Manager) considered a plus.

Cincinnati - Microbiology Technician

Science Job Classification: Contract Description:Microbiology TechnicianThe technician for this position will be performing basic micro work such as media prep, plating, streaking, pipetting, and cell counting on a daily basis. These tests will be performed on raw in-process and finished products.The ideal candidate will have a BS in Microbiology or Biology with 6 months to 3 years of experience. This is a first shift position Monday through Friday.CompetenciesDesired:PLATING, STREAKING, CELL COUNTING Contact Information Contact: Fields,Jennifer L

Cincinnati - Data Analyst

Classification: Full Time Compensation: $45000 to $55000 per year A well respected Cincinnati based company is actively seeking a Data Analyst to join their team. The Data Analyst will develop, maintain and enhance mechanisms to track, trend, and report quality measures to support the continuous quality improvement process needs of the Quality Department through comprehensive analysis and documentation of data pertaining to company performance goals. The Data Analyst will compile and analyze data including comparison of outcome measures to benchmark, identify trends, complete barrier analysis, and assist in the identification of activities to reach performance goals. Job Requirements JOB REQUIREMENTS: Education and Experience: • Bachelor's degree in business, science, healthcare or related field preferred. Equivalent experience considered. • 2+ years data analysis or statistical experience. • Proficient with window based environment, particularly Microsoft Excel and Access. Working knowledge of information systems including database design and SQL. • Previous HMO/Managed Care industry experience preferred. • Knowledge of SPSS preferred. • Understanding of ICD-9 and CPT coding system helpful. • Excellent analytic skills, attention to detail. • Detailed familiarity with computer systems, word processing, spreadsheet, statistical packages and other data base management software. • Good organizational skills; the ability to handle multiple priorities simultaneously with a high quality result. • Excellent writing skills. • Appreciation of cultural diversity towards target population

Cincinnati - Now You Can Go On More Vacations2894293

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Cincinnati - Chemist Job-7196_NM

Job Description: Responsible for implementing & leading projects requiring a basic understanding of the relevant fundamental theoretical aspects of the objective and sufficient laboratory experience to independently obtain meaningful results. The person in this position will be responsible for new product development, formulating optimization, performance evaluation, customer complaint investigation, and trouble shooting. Required to work independently with a minimum of supervision. Requires bachelor’s degree in chemistry or chemical engineering. A minimum of two years full time ink experience in a testing, research or development laboratory required; experience in formulating, color matching, troubleshooting, etc. in water-based inks environment preferred; experience working with customers is desirable. Required Skills; Formulation experience and Organic Chemistry experience. ● BACKGROUND & DRUG TEST ARE MANDATORY FOR THIS POSITION For FASTER Response: Please send your resume to: jobs@olsaresources.com Email subject line: Chemist Job-7196_NM OLSA Resources ® is a National Superior Staffing and Engineering Firm celebrating our 10th anniversary. We are a diverse company which employ’s professionals in many Sectors including Aerospace – Automotive – Business – Information Technology and Light Industry. We have successfully managed both outsourced and onsite projects. We are growing rapidly and in search for great new employees to come and join our successful future.

Cincinnati - Development Chemist

A growing mid-sized independently owned international packaging and ink company focused on water-based and UV cured inks for liquid packaging, flexible packaging, envelopes, corrugated, tags and labels and folding cartons is seeking a hands-on bench R&D Chemist. Responsibilities include: •Ensure development projects are completed within set time parameters. •Product improvement and enhancement of existing products to increase quality, performance, cost effectiveness. •Creative team player who can take ownership of projects to follow through from concept of project, production scale up and customer launch/commercialization. •Ability to effectively communicate with all levels of an organization. •Thoroughly document in process and completed work in well written reports and communicate results to the appropriate personnel in the company. •Creative team player with an internal/external customer focus. •Keep current with trends and new technology in the industry. REQUIREMENTS: •B.S. degree in Chemistry minimum, advanced degree preferred. •Experience in UV cured technology for Flexo Inks and adhesives for narrow web labeling a must. •Polymer chemistry training, knowledge of pigment chemistry and narrow web label market along with industry contacts. •Proven track record of developing successfully commercialized products. •Proficient in Microsoft office software. Please make reference to JOB ID: 3005 Only those candidates selected for interviews will be contacted.

Cincinnati - R & D Chemist

A dynamic successful growth oriented global company who manufactures coatings and chemicals is seeking a hands-on bench R&D Chemist for their Packaging Coatings division located in the Midwest. In a state-of-the-art, modern laboratory the incumbent will lead the product development of coating solutions for new and existing customers for UV curable non rigid packaging adhesives and pressure sensitive laminating adhesives. Responsibilities include: •Manage and prioritize projects to meet the expectations and needs of customers. •Ensure development projects are completed within set time parameters. •Product improvement and enhancement of existing products to increase quality, performance, cost effectiveness. •Take ownership of projects to follow through from concept of project to launch and commercialization. •Thoroughly document in process and completed work in well written reports and communicate results to the appropriate personnel in the company. •Keep current with trends and new technology in the industry. REQUIREMENTS: •B.S. degree in Chemistry. •Five years experience in the formulation and development of UV curable products for non-rigid packaging and laminating adhesives. •Proven track record of developing successfully commercialized products. •Proficient in Microsoft office software. Please make reference to JOB ID: 3004 Only those candidates selected for interviews will be contacted.

Cincinnati - R & D Chemist

A dynamic successful growth oriented global company who manufactures coatings and chemicals is seeking a hands-on bench R&D Chemist for their Packaging Coatings division located in the Midwest. In a state-of-the-art, modern laboratory the incumbent will lead the product development of coating solutions for new and existing customers. Responsibilities include: •Manage and prioritize projects to meet the expectations and needs of customers. •Ensure development projects are completed within set time parameters. •Product improvement and enhancement of existing products to increase quality, performance, cost effectiveness. •Take ownership of projects to follow through from concept of project to launch and commercialization. •Thoroughly document in process and completed work in well written reports and communicate results to the appropriate personnel in the company. •Keep current with trends and new technology in the industry. REQUIREMENTS: •B.S. degree in Chemistry. •Two years experience in the formulation and development of epoxy/phenolic and melamine chemistry for beverage containers. •Proven track record of developing successfully commercialized coatings. •Proficient in Microsoft office software. Please make reference to JOB ID: 3003 Only those candidates selected for interviews will be contacted.

Cincinnati - Medical Proposal Writer needed for Mt. Auburn Mgt Co

Classification: Temporary Compensation: Pay up to $13 per hour A World wide company based in the Clifton area is in need of a Proposal Writer for their home office. This job involves the proposal writing process from start to finish. The process for this position involves researching the Internet for requests for proposals, creating and submitting the proposals. A background in technical writing or grant/proposal writing is extremely helpful for this position as well as attention to detail. This is a business development research position. This position involves low supervision, so being self-directed is necessary to be successful in this position. A background in the military can be helpful for the correct candidate. Experience with Microsoft Excel is necessary. The hours for this position are 11:00-8:00 Monday- Friday. All applicants applying for U.S. job openings must be authorized to work in the United States. All applicants applying for Canadian job openings must be authorized to work in Canada. Job Requirements Requirements include 3+ years medical proposal writing experience. Must be familiar with research, creating and submitting proposals. Technical writing or grant writing is extremely helpful.

Cincinnati - Chemist - Formulation & Organic Chemistry ** DIRECT HIRE**

DIRECT HIRE POSITION for a CHEMIST that must have Formulation and Organic Chemistry experience. JOB DESCRIPTION: Responsible for implementing & leading projects requiring a basic understanding of the relevant fundamental theoretical aspects of the objective and sufficient laboratory experience to independently obtain meaningful results. The person in this position will be responsible for new product development, formulating optimization, performance evaluation, customer complaint investigation, and trouble shooting. Required to work independently with a minimum of supervision. A minimum of two years full time ink experience in a testing, research or development laboratory required; experience in formulating, color matching, troubleshooting, etc. in water-based inks environment preferred; experience working with customers is desirable EDUCATION: Requires bachelor’s degree in chemistry or chemical engineering. Please make sure you send in your desired salary requirements with resume.

Cincinnati - Lab Technician

Job Description Technical Specialist will provide direct support for sales, customers, technology and manufactruing of preparations products. They conduct performance evaluation testing, handle customer complaint investigation and new product development work. Technical Specialist are required to work independently with a minimum of supervision. Technical Specialists may be assigned to various tasks (technical assistance request, customer complaint investigation, new product development, and scale ups) and can expect to be cross-trained. They report directly to the Technical Service Managers. Technical Specialist take responsibility for and resolve product quality issues on a timely basis and conduct product performance evaluation on a daily basis. They are expected to interact with greater frequency and provide consistent support to sales, customers, technology and manufacturing of preparations. In addition to the requirements for laboratory technician, the employee would have a minimum of five years experience working in water-based ink industry. Providing immediate support for Manufacturing. Requirements for laboratory technicians are, depending on work area, proven experience performing raw material, work-in-process, or finished goods inspection and testing with minimal supervision. A cadidate may be accepted at the Technical Specialist level if having similar title at previous employment in a pigment, dipersion, or ink company. The Technical Specialist position is fully functional in all aspects of the Department. Must have consistently demonstrated initiative, dependability and sound judgement in addition to technical aspects of the position. Having experience in formulating, color matching, troubleshooting, etc. in ink enviroment would be considered to be a strength. Requires high school diploma, some college chemistry; four year degree preferred. Job Title: Lab Technician Primary Skills: Ink; Pigment Job Industry: Chemicals Vacancies: 1 Job City: Cincinnati Job Metro Area: Cincinnati Job State: OH Job Country: US Salary: DOE Hours per Week: 40 Start Date: ASAP Job Duration: Contract to Direct Detailed Job Duration: NA Degree Type: BS Degree Area: Chemistry Experience Minimum: 5 Years Certificates/Licenses: Job Requirements Ink; Pigment BachelorChemistry Candidates responding to this posting must currently possess the eligibility to work in the United States.

Cincinnati - Analytical Chemist

Job Description Kim Clark 2nd Shift Basic Function; The Analytical Chemist provides direct support for manufacturing with testing of raw materials, work in process and finished product. The Analytical Chemist works with little or no supervision to meet testing plans focused primarily on instrumental techniques. In addition, the Analytical chemist may be assigned to specific programs for equipment maintenance or calibration, creating batch reports and analyzing data. The Analytical Chemist must be proactive in performing tasks, pay close attention to detail, and meet or exceed expectations on data gathering and analysis. A qualified candidate must be able to perform all daily requirements for testing and recording without supervision. Basic qualifications; Education; A BS or BA in Chemistry is required with analytical chemistry preferred. A BS or BA in a scientific field with proven analytical experience will be considered. Experience; This is an entry level position. Some work experience in an analytical lab would be preferred. Job Title: Analytical Chemist Primary Skills: Chemist Job Industry: Chemicals Vacancies: 1 Job City: Amelia Job Metro Area: Amelia Job State: OH Job Country: US Salary: $40000/YEARLY To $40000/YEARLY Hours per Week: 40 Start Date: ASAP Job Duration: Direct Placement Detailed Job Duration: NA Degree Type: BS Degree Area: Chemistry Experience Minimum: 1 Years Certificates/Licenses: Job Requirements Chemist BachelorChemistry Candidates responding to this posting must currently possess the eligibility to work in the United States.

Cincinnati - Geologist

Engineering Job Classification: Contract Description:A national environmental/geotechnical and engineering firm is looking for a Staff Geologist to move into a Project Management role in the Cincinnati area. Requirements0-3ye ars experience, duties may include planning and implementing field investigations (preparation of work plans, coordination with oversight of subcontractors, logging of boreholes and construction of monitoring wells, environmental sampling, record keeping, analyzing and interpreting geologic, hydrologic and analytical reports.CompetenciesDesired:GEOLOGIST, GEOLOGIST PHASE I, ENVIRONMENTAL FIELD SAMPLING, GEOTECHNICAL DRILLING, RETAIL PETROLEUM, UNDERGROUND STORAGE TANK Contact Information Contact: Brewer,Sean P