Associate III, Quality Control, Bioassay & Virology

The role primarily supports M-F day shift. Candidates must be willing to support rotational weekend work (likely every other weekend) as required to meet project timelines and operational priorities.

About This Role

The QC Bioassay & Virology group in RTP, NC has an opportunity for an Associate III within the release and stability testing team. The group supports Quality Control testing of GMP samples using a broad range of biological analytical methods, including bioassays, cell-based assays, PCR, ELISAs, potency and binding assays. The team also provides reagent qualification testing, validation and transfer of analytical methods, and technical support of QC investigations.

This role requires strong technical expertise, excellent communication, and the ability to work independently, collaboratively within a team, and across business functions.

What You’ll Do

• Perform release and stability testing of drug substance materials using bioassays, cell-based assays, ELISAs, PCR, and other biological methods.
• Support laboratory operations including media preparation, inventory management, and equipment maintenance.
• Review data and documentation in a timely manner and ensure accuracy and compliance.
• Execute method transfers, reagent qualification, analytical improvement projects, and validation of analytical methods in collaboration with internal and external partners.
• Support maintenance of laboratory systems to ensure data integrity and regulatory compliance.

Who You Are

You are detail-oriented, scientifically curious, and thrive in a GMP laboratory environment. You have strong aseptic and cell culture technique, with the ability to troubleshoot and adapt. You are collaborative, eager to learn, and able to manage multiple priorities effectively.

Required Skills

• Bachelor’s degree in Biological Sciences
• Minimum 2 years of hands-on experience with cell culture techniques and biological testing (bioassays, ELISAs, PCR, potency/binding assays) within a GMP biotech manufacturing environment
• Excellent laboratory technique, experimental design, and documentation practices
• Strong organizational, time management, and prioritization skills
• Excellent oral and written communication skills

Preferred Skills

• Experience in virology methods and cell-based analytical testing
• Experience with statistical experimental design and data analysis (JMP, Excel)
• Experience with LIMS-based laboratory result reporting
• Relevant experience in reagent qualification, method validation and transfer

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.

Benefits

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.