• Manager Quality Assurance Disposition Support

    Bristol Myers Squibb (Devens, MA)
    …in a regulated industry with 1+ year quality experience. Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred. + ... Demonstrated experience with electronic system and databases + Ability to research, understand, intepret and apply internal policies and regulatory guidelines + Proficient computer skills with knowledge of several digital tools like MS Office, Smartsheets etc.… more
    Bristol Myers Squibb (01/09/26)
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  • Sanitation Technician

    Actalent (New London, WI)
    …Skills & Qualifications + Sanitation certification or relevant experience. + Experience with FDA regulations. Job Type & Location This is a Permanent position based ... out of New London, WI. Pay and Benefits The pay range for this position is $48000.00 - $52000.00/yr. 2 weeks vacation accrued sick pay accrues 2 hours per month medical, dental and vision benefits available upon hire company paid life insurance, short term… more
    Actalent (01/09/26)
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  • Thought Leader Liaison, PAH / PH-ILD

    Chiesi (Cary, NC)
    …created position will initially focus on pre-launch preparation in anticipation of FDA approval of our PAH/PH-ILD collaboration asset. They work closely with ... commercial colleagues, alliance partners and other staff to help build advocacy with KOLs. The Thought Leader Liaison also manages speakers, and captures KOL beliefs/insights, among other duties and responsibilities. This field-based position requires an… more
    Chiesi (01/09/26)
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  • Phlebotomist

    CSL Plasma (Chattanooga, TN)
    …donor disconnect. * In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin pheresis process. * Evaluates ... vein performance of the donor to identify possible problems; makes necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments when necessary to make the… more
    CSL Plasma (01/09/26)
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  • IU- Territory Manager

    Teleflex (Raleigh, NC)
    …to organizational goals, policies, procedures, good manufacturing practices, and FDA regulations, including strict compliance with applicable policies and ... regulations for both product lines. * Maintain a professional and credible image with key stakeholders, including physicians, consultants, suppliers, and teammates, for both UroLift System and Barrigel Rectal Spacer products. * Establish and maintain necessary… more
    Teleflex (01/09/26)
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  • Manager, Parenteral Manufacturing - Isolation…

    Bristol Myers Squibb (Manati, PR)
    …aseptic techniques.** + **Proficient in regulatory compliance, including cGMPs , FDA regulations, and Environmental Health and Safety (EHS) standards.** + **Skilled ... in interpreting and applying quality systems, documentation practices, and validation protocols.** + **Leadership & Interpersonal Skills:** + **Proven ability to lead cross-functional teams, drive performance, and foster a culture of accountability and… more
    Bristol Myers Squibb (01/09/26)
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  • Staff Engineer, Process Development - Cleaning

    Stryker (Tempe, AZ)
    …with PLC/Ladder Logic and other programming software. + Experience in an FDA regulated or regulated industry preferred. + Experience with cleaning processes, ... cleaning system design, cleaning equipment, and cleaning chemicals relating to medical device reprocessing including flushing, sonication, spraying, washing, rinsing, and drying. + Experience with water systems including Soft Water, RO and RODI. **Work… more
    Stryker (01/09/26)
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  • Manufacturing Supervisor - 1st Shift

    Zimmer Biomet (Warsaw, IN)
    …in a timely manner. + Responsible for day-to-day compliance and adherence to FDA QSR requirements. + Perform spot quality checks, 5S audits, Layered Process Audits. ... + Help drive/ lead continuous improvement projects. + Ensure team members are up to date and trained to perform assigned functions, including, but not limited to the areas of GMP, EHS and Quality Systems. + Ensure management is informed of all significant… more
    Zimmer Biomet (01/09/26)
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  • Quality Specialist Document Control

    PCI Pharma Services (Philadelphia, PA)
    …+ Strong interpersonal skills. + Basic knowledge of Lean Six Sigma and FDA cGMP's preferred. + Experience in Pharmaceutical industry preferred. + Experience in ... Printed industry preferred. **LANGUAGE SKILLS:** + Good Communication Skills-Written and verbal. **KNOWLEDGE/SKILLS REQUIREMENTS:** + Communication Skills: Written, Oral, Presentation, Candid, and direct feedback. + Technical Skills: Computer Literate… more
    PCI Pharma Services (01/09/26)
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  • Quality Technician

    Kelly Services (West Chester, OH)
    …SAP, KRONOS. + Experience in LEAN manufacturing and knowledge of cGMPs and FDA policies. **For more information or to be considered, please send resumes to** ... **###@kellyscientific.com** **or call ###.** As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical,… more
    Kelly Services (01/09/26)
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