Trackwise Jobs

Pfizer is hiring a QA Manager, Investigation Review to lead complex cGXP investigations, drive quality improvements, and represent QA across cross-functional teams at the Sanford, NC facility.

Eurofins seeks an experienced Analytical Biochemist in Indianapolis to run advanced analytical assays, support method qualifications and investigations, and mentor junior lab staff.

Intuitive seeks a data-focused RAQA Data Analyst 2 to transform cross-system quality and regulatory data into actionable dashboards and insights that support product quality, compliance, and investigations.

AbbVie's Branchburg site is hiring a Validation Engineer III to lead commissioning, qualification and validation efforts for equipment and processes in a regulated manufacturing environment.

Bristol Myers Squibb seeks a Specialist, Investigations to lead deviation investigations and CAPA activities within its cGMP cell therapy manufacturing site in Devens, MA.

Experienced quality compliance leader needed to own GxP inspection readiness, vendor audits, and quality system oversight at Rezolute's Redwood City office.

Eurofins seeks an Analytical Chemist in Indianapolis to execute medium- to high-complexity analytical testing and support method qualifications across chromatography and spectroscopy platforms.

Vertex is seeking a Senior QA Specialist (2nd shift, contract) to drive GMP-compliant product disposition and on‑floor quality oversight for cell and gene therapy drug product operations.

Lead critical cGMP manufacturing operations for Biogen's large-scale cell culture team by executing processes, coaching associates, and ensuring high-quality documentation and compliance.

Catalent is hiring an on-site Associate Scientist in Winchester, KY to support analytical method development, validation, and routine release/stability testing for clinical and registration programs.

OrganOx seeks a CAPA Manager to lead CAPA administration and reporting at its Giralda Farms US site, ensuring regulatory compliance and data-driven continuous improvement.

AbbVie’s Product Development team is hiring a Systems Engineer to own DHF management and ensure traceable, audit-ready design control documentation for on-market medical devices and combination products.

Medtronic is hiring a Quality Systems Business Analyst in Northridge to support and optimize eQMS processes and quality metrics for the Diabetes business, ensuring regulatory compliance and continuous improvement.

Experienced QA professional needed to lead GMP quality oversight, batch disposition, and investigations for drug product operations at a client site supporting clinical and commercial manufacturing.

CSL Plasma is hiring a Quality Specialist to manage center-level QA reviews, training coordination and compliance activities at the Topeka plasma center.

Experienced packaging engineer needed to lead development and qualification of primary, secondary, and tertiary packaging solutions for biologics, parenterals, and combination products at a leading pharmaceutical company.