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Senior Manager Quality Assurance Incoming Quality Raw Materials​/Disposition

Job in Holly Springs, Wake County, North Carolina, 27540, USA
Listing for: BioSpace
Full Time position
Listed on 2026-01-22
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Job Description & How to Apply Below
Position: Senior Manager Quality Assurance  Incoming Quality Raw Materials /Disposition

Join Amgens Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission to serve patients living with serious illnesses drives all that we do.

Senior Manager Quality Assurance Incoming Quality Assurance Raw Materials /Disposition What You Will Do

Lets do this! Lets change the world!

In this vital role, you will lead a team of Quality professionals supporting the Disposition and Incoming Quality operations at our North Carolina site. You will provide technical quality leadership and oversight of Disposition and Incoming Quality, partnering closely with cross‑functional teams to build, enhance and sustain compliant commercial operations.

  • Lead, manage, and motivate a high‑performing team of Quality professionals across key areas, including QA support for Disposition and Incoming QA, and their applicable quality systems (e.g., Document Management, Change Control, and Deviations).
  • Ensure team members are properly trained and qualified to perform their duties in accordance with cGMP and regulatory requirements.
  • Oversee workload distribution, resource planning, and departmental budgeting, including forecasting and monitoring.
  • Own the development, implementation, and continuous improvement of the site’s inspection readiness program and overall Quality Management System (QMS), ensuring compliance with Amgen standards, cGMP, and applicable regulations.
  • Ensure timely review, approval, and tracking of key cGMP processes, documents, and records, including deviations, CAPAs, Change Controls, validation protocols, and assays.
  • Lead cross‑functional investigations of deviations, ensure appropriate documentation, and assess changes for potential product quality impact.
  • Stay current with regulatory developments and quality trends to maintain a compliant and forward‑thinking quality program.
  • Represent the Quality unit during internal and external audits and regulatory inspections.
  • Alert senior management to significant quality, compliance, supply, or safety risks, using sound judgment and cross‑functional coordination when needed.
  • Manage hiring, succession planning, and performance development to ensure organizational capability and talent pipeline.
What We Expect Of You

We are all different, yet we all use our unique contributions to serve patients! The Manager Quality Control professional we seek is a strong leader with these qualifications.

Basic Qualifications
  • High school diploma / GED and 12 years of Quality and Manufacturing support industry experience OR
  • Associates degree and 10 years of Quality and Manufacturing support industry experience OR
  • Bachelors degree and 8 years of Quality and Manufacturing support industry experience OR
  • Masters degree and 6 years of Quality and Manufacturing support industry experience OR
  • Doctorate degree and 2 years of Quality and Manufacturing support industry experience
Preferred Qualifications
  • Educational background in Life Science and/or Engineering
  • Proven experience in Quality oversight of Incoming, Warehouse, and Disposition, with a strong focus on quality systems.
  • In‑depth knowledge of cGMPs, regulatory requirements, and pharmaceutical processing, with demonstrated ability to apply compliance principles in practice.
  • Hands‑on experience with Disposition, Incoming, and Quality Systems—particularly investigations, corrective actions, and audit readiness.
  • Experience managing and interacting with regulatory and internal auditors.
  • Demonstrated leadership of Quality teams, with strong team development, collaboration, and mentoring skills.
  • Effective risk management, negotiation, and cross‑functional collaboration abilities.
  • Excellent written and verbal communication, facilitation, and presentation skills in both English and Spanish.
What You Can Expect Of Us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well‑being. From our competitive benefits to our collaborative culture, we support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several…

Position Requirements
10+ Years work experience
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