Head of Batch Release Reporting to the Site Head of Quality, the Head of Batch Release is accountable for batch release operations, is point of contact with CBER lot release, OMCL interactions, the annual product quality review, and complaint investigations at Seqirus in
TITLE:MQA Specialist – 3rd Shift WHO WE ARE Indivior is a global pharmaceutical company working to help change patients lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision is that all patients around
Vulcan Elements is manufacturing American rare-earth permanent magnets for a secure, resilient future. With a focus on national security and economic resiliency, we serve critical industries such as defense, aerospace, and automotive powering a high-technology future.
This is a full-time salaried position with Project Farma, a PerkinElmer company. The successful candidate will reside in one of Project Farmas primary markets and be willing to travel domestically to meet client project requests. Project
Quality Assurance Specialist Department: Quality Assurance Employment Type: Full Time Location: Research Triangle Park, NC Description Kriya is a biopharmaceutical company whose mission is to develop life-changing gene therapies for diseases affecting millions of patients around
AgencyDept of Health and Human Services DivisionSEC OFFICE - INFO TECH - NC FAST Job Classification TitleOperating Systems Software Manager I (NS) Position Number65013812 GradeDT11 About Us The North Carolina Department of Health and Human Services
QA Operations Head Join Novartis as our QA Operations Head and play a pivotal role in ensuring patients receive high-quality medicines that meet the highest standards of safety, compliance, and reliability. This is an opportunity to
Documentation Area Specialist I Support daily GMP manufacturing operations by performing production sampling, managing batch documentation and GLIMS activities, and coordinating with cross-functional stakeholders to ensure accurate, timely, and compliant execution of manufacturing processes that enable product
Associate Director Quality Assurance Department: Quality Reports To: Vice President, Regulatory Affairs, Drug Safety, Quality FLSA Status: Exempt Job Type: Full-time Location: Raleigh, NC (hybrid role) The Associate Director, Quality Assurance is responsible for supporting the
This job is with Biogen, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. This is a full time on-site
External Quality Operation Manager (GMP) Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do
The QA Specialist is responsible for ensuring the quality, safety, and regulatory compliance of Investigational Medicinal Products (IMPs) used in clinical trials worldwide. This role supports Good Manufacturing Practice (GMP) compliance by reviewing manufacturing, packaging, laboratory,
Company Description ChromaGenix supports biopharma innovators in overcoming complex drug development challenges by enabling more efficient, consistent, and scalable purification of advanced biologics such as AAVs, mRNA, and viral vectors. The company specializes in synthetic affinity
Quality Manager Lead all regulatory, quality control, and quality assurance activities at the site. Serve as the final authority for quality product release decisions for sale or supply. Act as the primary quality liaison with customers, regulatory
Director, Site Quality - Raleigh Indivior is a global pharmaceutical company working to help change patients lives by developing medicines to treat Opioid Use Disorder (OUD). Our vision is that all patients around the world will
Sr QA Operations Manager Kelly Science is seeking a Sr QA Operations Manager to join a growing team located in Raleigh, NC. Salary: $175,000/year Shift: Monday-Friday 1st Shift (Fully on-site) Employment Type: Full Time; Direct Hire
Director, Quality Control The Director, Quality Control provides strategic and operational leadership for all Quality Control (QC) activities supporting drug substance (DS) and drug product (DP) manufacturing at the site. This role is accountable for ensuring
Document Control Assistant Kelly Services is seeking a detail-oriented and positive Sample Management Coordinator to support daily GMP manufacturing operations in one of our customer facilities in Durham NC. This contract role involves hands-on coordination of
Supply Chain Functional Lead As the functional lead for the Supply Chain at the manufacturing site you are accountable for definition and execution of all activities required to ensure timely service to our customers. Reporting to
Director, Manufacturing Sterile Operations At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are