• Director - Quality Control

    Catalent Pharma Solutions (Madison, WI)
    …Quality Control** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... groups: Microbiology, Environmental Monitoring, Stability, Release and In-Process, Method Validation and Sample Management. Catalent is committed to a Patient… more
    Catalent Pharma Solutions (07/02/25)
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  • Senior Quality Specialist, IVD

    Kelly Services (Sunnyvale, CA)
    **Title: Sr. Quality Specialist** **Location: Sunnyvale, CA** **Job Type: 1-year Contract , Full-Time, On-Site (M-F: 1st Shift)** **Compensation: $70-$80/hour (DOE) + ... guidance for Market Specification, Functional Specification, Design Verification, Design Validation , Test Method Validation , Risk Assessments, and Design… more
    Kelly Services (06/26/25)
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  • Senior Associate Scientist, Disc Bioanalytical

    Charles River Laboratories (Mattawan, MI)
    …pharmacokinetic/pharmacodynamic studies. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and ... lead the lab staff in the completion of method validation studies + Provide support to staff members as...facilities. **About Charles River** Charles River is an early-stage contract research organization (CRO). We have built upon our… more
    Charles River Laboratories (06/19/25)
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  • Associate Scientist II, QC

    Catalent Pharma Solutions (St. Petersburg, FL)
    …**Quality Control** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... in-process materials, fill moisture, raw materials, and cleaning verification and validation samples according to the assigned specifications, methods and protocols.… more
    Catalent Pharma Solutions (06/19/25)
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  • QA Associate

    Kelly Services (West Chester, OH)
    …Science & Clinical is seeking a **QA Associate near West Chester, OH.** ** Contract position (~6 months)** **Shift:** 6pm-6am rotating 12 hour shifts (2-2-3 rotating ... QA activities such as batch release, change control, process validation , deviation investigations, SOPs, supplier management, distribution center management, and… more
    Kelly Services (06/18/25)
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  • Microbiologist II

    Teva Pharmaceuticals (Forest, VA)
    …set-up and qualification. * Responsible for supporting validation /qualification activities (process/equipment/facility). * Responsible for developing, transferring ... microbial organisms. * Responsible for preparing samples for shipment to contract labs as applicable. * Responsible for drafting/amending Standard Operating… more
    Teva Pharmaceuticals (06/11/25)
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  • QC Scientist

    Astrix Technology (San Diego, CA)
    …Onsite - San Diego, CA **Salary:** $90,000 - 95,000 **Duration:** 6-Month Contract -to-Hire **Key Responsibilities:** + Write and review study protocols and technical ... and root cause analysis + Coordinate analytical method transfers and validation with external subcontractors + Manage relationships with subcontractors to ensure… more
    Astrix Technology (06/10/25)
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  • Sr. Analytical Scientist

    Two95 International Inc. (Durham, NC)
    …(small molecules), Ph.D. with 5-7+ years. + Excellent method development and validation skills and routine analysis on pharmaceutical materials (including potent ... + Strong preference for an analytical scientist who either has worked within a contract analytical lab working with external clients or has worked within a pharma… more
    Two95 International Inc. (06/09/25)
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  • Automation Engineer I

    Charles River Laboratories (Charleston, SC)
    …capital expenditure approval, management of integration and suppliers, testing, and validation . This role will monitor existing automation for end of ... programming assistance to maintain current equipment and software/control systems. + Validation , Qualification and FAT/SAT experience a plus + Perform all other… more
    Charles River Laboratories (06/08/25)
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  • Principal Scientist, Specialty Testing (LCMS…

    ThermoFisher Scientific (Middleton, WI)
    …other scientific discipline required 12+ years of relevant experience in a pharmaceutical or analytical testing laboratory that provides the knowledge, skills, and ... technical management, mentoring, and customer scientific interface for the CDMO ( Contract Development & Manufacturing Organization) sector within the GMP business.… more
    ThermoFisher Scientific (07/23/25)
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