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Associate III, Quality Control Raw Materials

Biogen

Biogen

Quality Assurance
Research Triangle Park, Durham, NC, USA
USD 68k-88k / year + Equity
Posted on Dec 16, 2025

This position is a M-F business hours schedule (8A-5P) and is full time on-site at our RTP facility

About This Role
As an Associate III, QC Raw Materials, you will play an integral role in the Quality Control Raw Materials team at the Biogen RTP Pharma site. This critical position supports functional, tactical, and operational objectives by sampling, inspecting, and testing raw materials while maintaining strict adherence to cGMP documentation standards. Your expertise in Gas Chromatography (GC) and wet chemistry will be essential as you perform compendial testing and manage data entry into electronic laboratory information management and inventory systems. Collaborating closely with QC teams, Quality, Planning, Warehouse, Validation, and Manufacturing teams, you will help ensure that operations run smoothly. Your role may also involve assisting with GMP compliance activities, investigation writing, and continuous improvement initiatives. By working independently and as part of a team, you will contribute significantly to the success of our quality assurance goals.

What You’ll Do

  • Perform raw material sampling, inspections, and release testing.

  • Conduct utility monitor samples to ensure quality standards.

  • Provide technical review of data and documentation for QC Raw Materials.

  • Support investigations and QC operations in alignment with business and manufacturing schedules.

  • Assist in process validation initiatives to maintain compliance.

  • Maintain effective laboratory systems to ensure the integrity of results.

  • Collaborate with various teams to support laboratory compliance and personal development.

  • Enter data into electronic laboratory information management and inventory systems.

  • Manage retention samples and training to sustain 100% compliance.

Who You Are
You are a detail-oriented professional passionate about maintaining high standards of quality. You excel in both independent and team environments, leveraging your strong written and verbal communication skills to contribute effectively. Your problem-solving abilities and technical expertise in laboratory techniques make you a valuable asset to the team. You are dedicated to continuous improvement and ensure compliance with established processes and timelines.

Required Skills

  • Bachelor's degree in science or related field.

  • Minimum 2 years of relevant experience working in QC within a GMP pharma or biotech environment.

  • Experience with Gas Chromatography (GC) and wet chemistry per compendia.

  • Ability to move 50 lbs with the assistance of equipment as needed.

  • Demonstrated technical ability in fundamental laboratory techniques and analytical methodology.

  • Bachelor's degree in science or related field.

  • Strong organizational skills with the ability to multitask and coordinate multiple activities.

  • Excellent communication skills, both written and verbal.

  • Ability to interpret data and draw conclusions.


Job Level: Professional


Additional Information

The base compensation range for this role is: $68,000.00-$88,000.00


Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:

  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.