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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.

    Requirements:
    - 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: 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