• Merck & Co. (Rahway, NJ)
    Job Description SPECIALIST JOB DESCRIPTION - The Chemical Biotechnologies group within the Process Research & Development Enabling Technologies Department in Rahway, ... New Jersey, is seeking a Specialist to support and enhance our capabilities in high-throughput screening and automation for designing and engineering proteins with… more
    HireLifeScience (11/07/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Senior Automation Specialist provides end-to-end automation and quality engineering support for the Rahway, NJ FLEx (Formulation, Laboratory & ... and visualization to meet operational and compliance needs; keep documentation , SOPs, drawings, configurations, PMs, and inventories inspection-readyLead and… more
    HireLifeScience (11/14/25)
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  • embecta (Parsippany, NJ)
    …global employees. We are seeking a highly skilled and motivated NA **Payroll Specialist ** who will be responsible for all payroll related responsibilities in US, ... as required. + Participate in internal and external payroll audits, ensuring all documentation is accurate and compliant with SOX controls. + Create ad-hoc reports… more
    DirectEmployers Association (11/13/25)
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  • Aequor (Bend, OR)
    …and knowledge of GMP regulations Support implementation and continuous improvement of Quality Systems Control record management including receipt, reconciliation, ... scanning and verification, record check-out/check-in and maintain scanned record back-ups Controlled document issuance and tracking Support audit activities Controlled numbering issuance and tracking Perform other duties as assigned Work experience:… more
    HireLifeScience (11/12/25)
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  • SMBC (New York, NY)
    …with vendors on software releases and recommend internal changes.Develop documentation , guidelines, desktop procedures, dashboards, and ad-hoc analytics. + Ensure ... laws and data privacy regulations. + Demonstrate knowledge of continuous improvement methodologies and HRIS systems. **Qualifications and Skills** + Ability to… more
    DirectEmployers Association (09/25/25)
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  • Kedrion Biopharma (Fort Lee, NJ)
    …in Fort Lee, NJ. We're looking for a detail-oriented and proactive Logistics Specialist to join our US operations team. This role supports the coordination and ... cross-functionally to improve logistics network performance by identifying areas for improvement and implementing solutions. + Manage and track inventory to ensure… more
    DirectEmployers Association (09/18/25)
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  • Terumo Medical Corporation (Elkton, MD)
    Sr. Quality Systems Documentation Specialist Date: Nov 13, 2025 Req ID: 5082 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Quality ... **_Advancing healthcare with heart_** **Job Summary** The Senior Quality Systems Documentation Specialist will be responsible for developing, managing, and… more
    DirectEmployers Association (08/19/25)
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  • Merck & Co. (Lower Gwynedd, PA)
    …Description-The PDMB Regulated Bioanalytics Department is seeking a Compliane Senior Specialist and Technical Writer team within the Late Development (AdVAnce) ... otherwise coach department staff on maintaining adherence to SOPs and documentation requirements.-Participate or lead internal initiatives that result in quality… more
    HireLifeScience (11/15/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA ... Change Control Specialist II role is an exempt level position with...systems and cGMP requirements.Review change controls, SOPs, and other documentation .Require minimal direction to complete tasks, knows how to… more
    HireLifeScience (11/11/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey. ... Role OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...immediate path forward for manufacturing quality issues.Review of all documentation , in accordance with Good Documentation Practices… more
    HireLifeScience (11/04/25)
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