• Sr Director, R&D, Cytology

    Hologic (Marlborough, MA)
    …testing practices. + In-depth knowledge of medical device regulations and standards ( FDA , ISO, CE Mark). + Track record of leading successful product development ... projects from concept to commercialization. + Proven ability to inspire, build, and lead cross-functional teams in a matrixed, fast-paced environment. + Experience with lean methodologies and driving organizational transformation is highly valued. +… more
    Hologic (01/10/26)
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  • Lead Tech Writer -Doc Control

    Lilly (Pleasant Prairie, WI)
    …of GxP Procedural Documents, Protocols and Investigations to ensure compliance with FDA regulations and company policies and procedures. This role provides services ... in QA Initiatives and Cross Functional projects. Additionally, this role is responsible for the authoring, format, review, routing, distribution and filing of GXP documentation. This position requires a thorough knowledge of computer applications in the… more
    Lilly (01/10/26)
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  • Manager, Patient Materials Operations

    Bristol Myers Squibb (Summit, NJ)
    …12hr/7d Operation). The position assures individual and group compliance with all FDA , DEA, DOT, ISBT, CTPAT, OSHA, VAWD, cGMPs and applicable policies, regulations ... and certifications including training, documentation, standard operating procedures, and corporate policies while maintaining a culture of safety, compliance, innovation, and Continuous Improvement The scope of the Patient Materials Operation Manager role: +… more
    Bristol Myers Squibb (01/10/26)
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  • Operations Supervisor

    Keurig Dr Pepper (Lansing, MI)
    …safety codes, policies, and procedures of the Company and standards established by OSHA, FDA , and DOT. **Total Rewards:** + $70,500 - $85,000 / year + Actual ... placement within the compensation range may vary depending on experience, skills, and other factors + Benefits, subject to election and eligibility: Medical, Dental and Vision, Paid Time Off, 401(k) program with employer match, Child & Elder Care, Adoption… more
    Keurig Dr Pepper (01/10/26)
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  • QC Manager, Bioanalytical

    ThermoFisher Scientific (Plainville, MA)
    …fast-paced environment required. + Experience with regulatory inspections from the FDA , EMA, Health Canada, or other regulatory authorities required. **Knowledge, ... Skills, Abilities** + Capable of writing reports, business correspondence, and procedure manuals. + Strong organizational skills; ability to prioritize and lead through complex processes/projects. + Ability to read, analyze, and interpret business periodicals,… more
    ThermoFisher Scientific (01/10/26)
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  • Electro-Mechanical Assembler

    ManpowerGroup (Salem, MA)
    …accuracy. + Keep work area clean and follow safety guidelines (OSHA, FDA , CDC). **What's Needed?** + 2+ years of electromechanical assembly experience (preferred) ... + Comfortable working with pneumatic systems, including installation and troubleshooting of compression fittings. + Attention to detail, the ability to build to bill of materials or assembly drawings, and proficiency in using hand and power tools are… more
    ManpowerGroup (01/10/26)
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  • Medical Information Specialist II

    Adecco US, Inc. (Morristown, NJ)
    …provides summaries of literature searches for NDA product annual reports for FDA submissions. * interacts with contact center team(s) and coordinates meetings, ... trainings and exchange as needed * performs regular contact center quality checks in US * supports training of support function staff and outsourced partner(s) as needed. * executes processes and participates in cross functional projects by contributing with… more
    Adecco US, Inc. (01/10/26)
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  • 3rd Shift Maintenance Technician

    Aerotek (Holland, MI)
    …sq. ft. of space. The environment is clean and temperature-controlled, meeting all FDA requirements. Most of the facility is maintained at 55 degrees, with some ... areas at cooler temperatures. A supportive team environment ensures that employees look out for each other. Standard steel-toed boots are required, with some liquid resistance preferred. The facility houses over 500 employees and produces frozen food for… more
    Aerotek (01/10/26)
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  • Senior Microbiologist Sterilization

    Medtronic (North Haven, CT)
    …in Engineering, Microbiology, or related technical discipline. + Familiarity with FDA , EU and other international regulations, standards and guidelines governing ... sterilization of medical devices. + Experience conducting clean room contamination investigations. + Strong familiarity with ISO 14644 series, EU 17141 / ISO 14698. + Experience with microbiological laboratory test methods including bioburden, BET, microbial… more
    Medtronic (01/10/26)
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  • Quality Technical Reviewer - Celsis

    Charles River Laboratories (Charleston, SC)
    …We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years. We're committed to providing benefits that elevate your ... quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.… more
    Charles River Laboratories (01/10/26)
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