About this role
About This Role As a QA Associate III, you will apply strong knowledge of cGMP requirements, Biogen Quality Systems, internal procedures and your primary quality discipline to support compliant manufacturing operations. You will review and approve documentation that supports batch and cell bank disposition, assess product acceptability for continued processing or distribution, and provide timely quality direction on the manufacturing floor. You will partner across Quality, Manufacturing and PO&T to identify and resolve quality and compliance concerns, support inspection readiness and advance new product introduction technology transfers and restart programs.
You will also provide technical writing and investigation support, including root cause and impact assessments, and may complete selected minor investigation or GCC assessment activities after demonstrating the required competencies and with management oversight. This individual contributor role requires sound judgment, mature situational leadership and the ability to work independently while collaborating across functions and organizational levels. What You’ll Do Review and approve batch and cell bank disposition documentation for cGMP compliance and product acceptability Review executed BPRs, PRCDs/WIs, formulas, recipes, validity rules, MPRs, MSLRs, MSMs, PCDs, PFDs and PARs Perform manufacturing-floor record review, observations, WORCs and inspection-readiness walkthroughs Provide quality oversight of manufacturing operations and technical consultation on regulatory and site-procedure requirements Support resolution of technical and compliance issues or gaps of low to moderate complexity Support the QA Lead for NPI technology transfers and restart programs Provide technical writing, investigation support, root cause analysis and impact assessment Support CAPA closure and review or approval of associated documentation with management oversight Assist with implementation of Quality Management Systems and GxP quality-systems training Communicate quality issues, recommendations and decisions across Quality, Manufacturing, Engineering, Warehouse, and other functions Who You Are You are a detail-oriented quality professional who applies sound judgment, regulatory knowledge and a practical understanding of manufacturing to protect product quality.
You communicate complex information clearly, adapt to changing priorities and build productive cross-functional partnerships to resolve issues and maintain compliance. Required Skills Bachelor’s Degree required , preferred in a life science discipline 2+ years of related experience working in a quality GMP biopharma or pharma environment Working knowledge of GxP regulations, cGMP requirements and relevant FDA/EMA expectations Understanding of quality systems, quality concepts and manufacturing processes Strong organization, prioritization and multi-tasking skills Excellent written, verbal and interpersonal communication skills Preferred Skills Investigation, root cause analysis, impact assessment and technical writing skills including d emonstrated competency in minor investigations, CAPA documentation or GCC assessments Experience reviewing controlled manufacturing and disposition documentation Understanding of biopharma or pharma manufacturing processes Job Level: Professional Additional Information The base compensation range for this role is: $69,000.00-$90,000.00 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 Biogen. 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.