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4 laboratory manager jobs found

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Avantor
Full time
 
Freezer/Sample Management Coordinator
Avantor Malvern, PA, USA
The Opportunity: In this role, you will report to the Onsite Manager and will work closely with the Avantor’s Advanced Laboratory Services professionals to serve our customers by performing customized, mission-based lab work and research protocols that help return time back to science. Location: Spring House, PA Shift: Monday - Friday 8:00 AM - 4:30 PM Hourly Rate: $21.00 - $24.00 Benefits: Health and Wellness: Medical, Dental, Vision, and Wellness programs Time Off: Paid Time Off (PTO), Company-paid holidays, Choice holidays, etc. Financial Well Being: Spending Accounts: Flexible Spending Account (FSA), Health Savings Accounts (HSA), commuter benefits, 401(k), tuition assistance, employee stock purchase plan discount Added Protection Coverage: To include critical illness, hospital indemnity, accident, legal, identity theft protection, pet, auto, and home insurance Recognition: Celebrate your peers and earn points to redeem...

Apr 05, 2026
BM
Full time
 
Manager, GMP Inspection Management
BristolMyers Squibb Indianapolis, IN, USA
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you'll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact-on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/ Summary The Manager, GMP Inspection Management provides management of activities for Site Quality Operations in accordance with RayzeBio policies, standards, procedures and global cGMPs. In addition, the role will be responsible for the Self-Inspection Program,...

Mar 21, 2026
Vertex Pharmaceuticals
Full time
 
Associate Director, Audit Management
Vertex Pharmaceuticals Boston, MA, USA
Job Description General Summary: The Audit Management Associate Director is responsible for the audit and inspection management for assigned activities, inclusive of internal and external processes. This role has responsibility for design and execution of compliance audits primarily across GCP/GLP suppliers and clinical investigator sites through the development of a risk-based audit program designed to support activities across Vertex business functions. This role ensures adherence to applicable regulations, industry standards, and to Vertex policies, procedures, and quality standards as set forth in the Quality Management System. This role may be a generalist but more often specializes in laboratory or clinical practices. Regularly applies specialized domain knowledge to assignments and provides technical recommendations to management. May have people management responsibilities within the organization including financial accountabilities and human resource...

Mar 15, 2026
Unilever
Full time
 
Quality Management Systems (QMS) Specialist
Unilever Chicago, IL, USA
JOB PURPOSE The QMS Specialist plays a critical role in driving our manufacturing site toward World Class Manufacturing (WCM) standards, anchored in zero defects, zero waste, and zero losses. This position champions the deployment of Focused Improvement (FI) and Quality Improvement methodologies to reduce quality related losses and elevate cross functional performance. Acting as a key link between Production, Quality, and Logistics, the role ensures seamless end to end processes that uphold regulatory compliance, product integrity, and operational excellence. KEY RESPONSIBILITIES Quality Support & Expertise Provide daily quality support to production and logistics teams, ensuring timely investigation and resolution of quality issues. Own and maintain the site’s document control system, ensuring timely revisions of controlled documents, accurate change management, and full compliance with SOP requirements. Develop and implement inspection procedures, validation...

Apr 04, 2026
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