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  • Valid City, State or Zip Code: Maxton
    Job Type : Contract
    Date: Friday, 19 April 2019
    The Aseptic Technician I is a core team member of the manufacturing team. The Aseptic Technician I is responsible for daily production including environmental monitoring, formulating, and sterile filling of aseptic GMP manufactured products according to batch records and SOPs. This position allows for exposure to many department's ways of working and opportunities for cross-functional projects. Allows for insight into the world of biotechnology.

    - Science background
    - 4 year biology degree
    - Aseptic background
  • Valid City, State or Zip Code: Quincy
    Job Type : Temporary
    Date: Thursday, 18 April 2019
    What's in it for you?

    * Full Time hours 40 per week
    * Sunday night through Thursday night: Shift start = 10:30 pm / Shift end = 7:00am.
    * Competitive wages $17/hr.
    * Weekly Pay

    What is the job?

    Perform all duties to ensure proper physical and systematic pick, sort, put away and replenishment of medical devices, while identifying, resolving, or elevating issues in a timely manner. Understand and adhere to all SOP's / WI's and compliance requirements. Transact and process materials as required.

    * Accuracy of transactions and physical movement of product from pick, sort, put away, and replenishment areas.
    * Process warehouse tasks, meeting all specified product handling requirements.
    * Required training to Standard Operating instructions and follow processes with strict adherence. Daily housekeeping required. Adherence to work rules required. Adherence to safety rules required.
    * Daily housekeeping required. Adherence to work rules required. Adherence to safety rules required.
    * Use of computer devices, hand held scan guns, printers, product handling device -pallet jacks, other equipment as required.
    * Will involve riding on and operating an electric pallet jack

    What you bring to the job?

    * They will be required to have a valid Driver's License.
    * Lifting, standing, bending, reaching, pushing, pulling required.
    * Understanding of lean principles.
    * High School Diploma or Equivalent.
    * Previous Warehouse experience preferred, not mandatory
    * Will be operating an electric pallet jack - must pass DMV check

    Stop your job search and apply today. We love referrals so please share our job with friends and family.
  • Valid City, State or Zip Code: Allegan
    Job Type : Temporary
    Date: Thursday, 18 April 2019
    Calling all Rising Junior or Seniors working toward a bachelor's degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering or closely allied life sciences discipline, or scientific graduates within the 2018/19 academic year. We are seeking a summer student associate to work in R&D, beginning in May and concluding in August. This is a first shift position, 40 hours a week (some flexibility with start and end time). Pay rate 18/hr.

    What's in it for you?

    Weekends off

    Pay rate 18.00/hr

    Opportunity to use your education and passion for science

    What is the job?

    With guidance from an assigned mentor, complete a focused research project related to development activities underway in US Consumer Selfcare - Americas R&D for new or reformulated generic over-the-counter (OTC) pharmaceutical products.

    Properly assimilate principles of Perrigo's Positive Workplace Policies and Code of Conduct by demonstrating and reinforcing appropriate behaviors that foster a workplace of trust, commitment, and accountability while striving towards results.

    Expected Outcomes
    * Summer associate will gain pharmaceutical industrial experience in a cGMP qualified laboratory setting
    * Summer associate will strengthen instrumental analysis experience
    * Summer associate will develop professional relationships with scientists solving real world analytical challenges
    * Summer associate will present research findings to departmental colleagues and management

    What do you bring to the job?

    Strong analytical skills and data entry skills

    Good written and verbal communication and a strong attention to detail

    Ability to pass a Background Check and Drug Screen

    Stop your job search and apply today. Do you need more information? Contact Stephanie at Stephanie.Shoemaker@manpower.com. We love referrals so please share our job with friends and family. Also, check out Manpower's career platform with tools and resources to prepare you for today and tomorrow's jobs at www.manpower.com/mypath
  • Valid City, State or Zip Code: Rockville
    Job Type : Contract
    Date: Tuesday, 16 April 2019
    We are recruiting for an Associate who will perform safety testing required to manufacture clinical and commercial products. The associate is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of client services, technical principles and applications. ESSENTIAL JOB FUNCTIONS
    * Conducts assigned molecular testing with minimal supervision within constraints of lab scheduling.
    * Performs testing in accordance with SOPs and regulations (cGMP and GLP).
    * Maintains complete and comprehensive records for study integrity.
    * Makes detailed observations and documents results.
    * Operates and maintains lab equipment as required by SOPs and testing procedures.
    Other Duties as assigned.
  • Valid City, State or Zip Code: Frederick
    Job Type : Permanent
    Date: Tuesday, 16 April 2019
    Director of Quality
    Frederick, MD

    Do you bring 8+ years of Quality Management experience? Does your experience include working in a small biopharmaceutical company producing Phase I/II clinical materials, including vaccines and biotherapeutics? In this position, you'll be responsible for all aspects of quality assurance, from strategic planning to hands-on implementation, including:

    * Be responsible for the strategy, implementation and leadership of the QA and Regulatory function
    * Be accountable for the execution and administration of the GxP quality system pertaining to GMP and relevant ICH, US, and EU regulations
    * Manage a group of at least 35 employees reporting into 8 quality assurance functions
    * Ensure appropriate quality oversight of external vendors, e.g., contact manufacturing organization (CMO), contract testing labs (CTL)
    * Plan and oversee day-to-day activities of the quality function including management of consultants, external auditors, internal quality functions, e.g., continuous improvement, training, compliance, document control, lot release, regulatory affairs, validation/calibration, and computer systems validation
    * Lead preparations and management of regulatory inspections and client audits

    Interested? Well qualified candidates will bring:
    * A Bachelor's degree in a related field of study, a Master's degree is preferred
    * Experience working in a small biopharmaceutical company producing Phase I/II clinical materials, including vaccines and biotherapeutics
    * At least twelve (12) years of experience in Quality Assurance including at least eight (8) years of management experience
    * Regulatory Affairs Certification (RAC)
    * Extensive knowledge and experience in GxP and QA principles, practices, regulatory and industry standards
    * Experience with using risk-based principles and decision making to ensure compliance at all stages of development
    * Strong negotiation skills
    * Must be able to obtain and maintain a clearance

    This position comes with a generous salary and complete benefits package close to home in Frederick.
    Apply today learn more about the Director of Quality position!
  • Valid City, State or Zip Code: Allegan
    Job Type : Contract
    Date: Wednesday, 03 April 2019
    Are you passionate about science and have an analytical mindset? Do you have a degree in Microbiology or a scientific related field? Manpower is partnering with Perrigo, a large pharmaceutical company in Allegan, Michigan to fill a long term temporary Microbiology Lab Technician. The candidate selected would provide analysis that supports the microbiological analysis of environmental monitoring samples through media preparation, sampling, sample testing, and review and validation of data. The individual will also possess good written and verbal communication skills, excellent documentation and organizational skills. They will have critical thinking skills, attention to detail, and the ability to work independently and with others. Lastly the individual will take ownership of assigned tasks and responsibility for the results. The requirements for this position include a high school diploma or equivalent, ability to pass a drug screen and background check. Don't delay, apply today

    First shift, Monday-Friday 8am-4pm, weekends off!
    pay rate:16/hr
  • Valid City, State or Zip Code: Ypsilanti
    Job Type : Temporary
    Date: Tuesday, 02 April 2019
    Manpower is seeking a Shipping and Receiving / Sample Handler for our client in Ypsilanti. This long-term, full-time position offers day time working hours (8:30am - 5pm) and pays $13.00 - 16.00 depending upon experience. The selected candidate will be packing and shipping test sample kits, receiving samples from the lab and ensuring samples meet all requirements. Must be able to lift-up to 50 lbs., stand for up to eight hours and possess strong computer, math and science skills. This is an excellent opportunity to work for a leading provider of quality laboratory services with a commitment to customer service. Contact our office to apply today: 734-665-3757 ext: 5. Get a head start by creating an account at manpower.com and then give us a call!
    Know of others looking for work? Please share this post! You could earn a $50 referral bonus for each successful referral.

    To see more openings with Manpower across Southeastern Michigan, visit manpowermi.com or follow us on social media.
    Manpower, Inc. of SE Michigan is an Equal Opportunity Employer.
  • Valid City, State or Zip Code: Shelton
    Job Type : Temporary
    Date: Wednesday, 27 March 2019
    Major Consumer Products Company in Trumbull, CT is looking for a Scientist for a full time position - initially 6 month assignment, but possibility of extension or temp-to-perm.
    This role will support category design library, identifying, requesting and updating technical documentation as well as bench formulation work.

    Technical Skills
    BS in Chemistry, Chemical Engineering or related field with 3-5 plus years of experience in product development
    Must have batching experience
    Demonstrates understanding of laboratory techniques and procedures for the evaluation of product functionality and stability.
    Demonstrates knowledge of the chemical, physical, and functional properties of raw materials.
    Must demonstrate basic understanding of experimental design techniques.

    Project Management Skills
    Plans, implements and evaluates formulation prototypes using standard scientific methods (i.e. statement of purpose, documented procedure, interpretation of results and conclusion).
    Demonstrates knowledge of the steps involved in the overall product development cycle.
    Understands the role, which all R&D functional areas play in the overall product development process.
    Effectively uses internal and external evaluation procedures as appropriate.

    Communication Skills
    Must demonstrate the ability to understand, follow instructions, guide and instruct others as needed.
    Prepares detailed reports and memos.
    Actively participate in and effectively conducts meetings with technical and non-technical personnel.
    With minimum supervisory input, must demonstrate the ability to present information to both technical and non-technical audiences.

    Interpersonal Skills
    Must have the ability to develop and maintain good working relationships.
    Must operate in an ethical manner, exhibiting self-confident integrity.
    Actively participates in a team environment.
    Must demonstrate flexibility and open-mindedness to achieve objectives.
    Must have the ability to supervise others on routine standardized procedures and techniques.
  • Valid City, State or Zip Code: Burlington
    Job Type : Contract
    Date: Wednesday, 27 March 2019
    Manpower is currently seeking a Tech Writer in the Life Science Industry.
    Job Summary
    This role will be dynamic and fast-paced and will require working cross-functionally with various departments to manage the technical writing requirements for the Life Science group.

    Responsibilities and Duties
    * Manage the overall coordination of tech writing projects.
    * Responsible for creating product notification letters and inserts.
    * Strong verbal and written communication skills
    * Planning, time management, organization, and attention to detail
    * Work with stakeholders to define and set priorities, deadlines and deliverable schedules.

    Qualifications and Skills
    * College diploma or university degree.
    * Good organization skills, including the ability to be flexible to changing priorities and needs.
    * Demonstrated attention to detail and accuracy combined with proven ability to multitask.
    * Ability to independently prioritize and execute tasks and responsibilities.
    * Excellent interpersonal skills with proven ability to get along well with others and work in a team environment; includes the ability to work with geographically remote teams and/or projects.
    * Demonstrated knowledge of personal computer software in a business environment including word processing, spreadsheet, and database applications (Microsoft Office platform preferred).
    * Knowledge of Adobe InDesign software and of life science biologic products required
    *Meticulous and can handle multiple assignments.
    Please send your resume today or call Donna Lungo for immediate consideration at
    (978) 685-7778
  • Valid City, State or Zip Code: Gaithersburg
    Job Type : Contract
    Date: Tuesday, 26 March 2019
    Job Duties May Include But are Not Limited To:
    * Restocking of lab supplies and reagents
    * Maintain and clean laboratory equipment such as centrifuges, laminar flow hoods, incubators, micropipettors, etc.
    * Perform autoclaving
    * Empty trash and recycle bins
    * Maintain a safe, neat, clean, and well organized laboratory work environment to support scientists
    * Responsible for performing, recording, and reporting data in a GLP (Good Laboratory Practices) compliant fashion
    * Receipt, storage, and disposal of test article
    * Preparation of sterile reagents
    * Daily equipment checks
    * Use of scales for measuring reagents and test articles
    * Preparing workspaces for assay performance
    * Miscellaneous duties as required to support laboratory and business operation
    Required Skills:
    * A working knowledge of the proper/safe handling of chemicals and hazardous materials
    * Demonstrated competence in basic mathematical skills
    * Ability to comprehend and follow written and verbal guidance
    * Demonstrated competence in the use of PC-based word processor and spreadsheet software
    * Effective written and verbal communication skills
    * Ability to work in a fast paced environment
    * Comfortable working independently and in a team oriented environment
    * Attention to detail
    * Must be capable of moving heavy objects (approximately 50lbs)
    * Must have reliable transportation

    Required Education: AA or AS degree in biological sciences or equivalent. 1 year of work experience performing similar duties in a scientific laboratory and/or vocational training in laboratory sciences can be used in lieu of education requirement.
    Job Type: Full-time
    Perform medical laboratory tests for the diagnosis, treatment, and prevention of disease. May work under the supervision of a medical technologist. Requires formal training and may involve scientific analysis or process development. Work does not require routine inspection, testing, grading, sorting, sampling, or weighing of either raw materials or processed products. See staffing description below for comparison.
  • Valid City, State or Zip Code: Holland
    Job Type : Contract
    Date: Tuesday, 26 March 2019
    Calling all weekend shift applicants with a life science degree..A large pharmaceutical company in Allegan MI is seeking someone like you who will be responsible for performing routine testing on raw materials and finished products in the Quality Control laboratory at their Holland, MI location. Job duties for the selected individual include but are not limited to: preparing sample/solutions per written procedures, identification and other physicals testing, maintaining accurate laboratory documentation according to pharmaceutical cGMP, use of laboratory equipment for analysis such as analytical balances, pH meter, UV-Vis spectrophotometer, HPLC, GC etc. Must be detail oriented, have the ability to multi-task and work well with other lab technicians to complete daily assignments. Excellent written and verbal communication skills required. Individual must be flexible to work different shifts to complete training and meet the needs of the company/department.

    *Will train on first shift

    Stop your job search and apply today, bring your life science degree, applicable lab experience and ability to pass a drug test and background check. We love referrals so please share this opportunity with friends and family.
  • Valid City, State or Zip Code: Geismar
    Job Type : Contract
    Date: Tuesday, 26 March 2019
    Manpower has immediate openings for Quality Analysts in Geismar, LA!

    We are seeking an Quality Control Analyst to join our team! You will be responsible for performing evaluation of final product, intermediate products, raw materials, and production facilities.

    What's in it for you?

    Opportunity to work for Fortune 100 Company
    Offers stability and longevity
    Competitive Benefits
    What is the job?

    Performing Quality Control assays, writing and establishing specifications, assisting in the validation of Quality Control assays, and writing Standard Operating Procedures.
    Responsible for evaluation of final product, intermediate products, raw materials, and production facilities.
    Relies on instructions and pre-established guidelines to perform the functions of the job.
    Works under immediate supervision. Typically reports to a manager.
    What do you bring to the job?

    Bachelor's degree in area of specialty and 0-2 years of experience in the field or in a related area.
    Must pass background/ drug test
    Do you need more information? Contact Angela at 414-269-3151 ext. 1219.We love referrals so please share our job with friends and family. Also, check out Manpower's career platform with tools and resources to prepare you for today and tomorrow's jobs at www.manpower.com/mypath