Sr Associate II, Technical Quality

Reposted 3 Days Ago
Be an Early Applicant
Triangle Trailer Park, Township of Jacksonville, NC, USA
In-Office
93K-121K Annually
Senior level
Biotech
The Role
Lead and oversee technical quality activities across manufacturing, lab, engineering, and quality operations. Manage deviations, root cause investigations, CAPA, change controls, material disposition, technology transfers, QC oversight, regulatory inspection readiness, and continuous improvement to ensure GMP compliance and operational excellence.
Summary Generated by Built In

About This Role

As a Senior Associate II, Technical Quality, you will play a critical role in ensuring quality and compliance across manufacturing, laboratory, engineering, and quality operations. You will lead and support investigations, change controls, quality oversight activities, and continuous improvement initiatives that strengthen operational performance and regulatory compliance. This position serves as a key technical quality subject matter expert, partnering cross-functionally to solve complex problems, assess risk, and implement effective quality solutions. You will provide quality assurance oversight for quality control activities, technology transfers, material management, and regulatory inspection readiness. This role helps drive a culture of quality, compliance, and operational excellence across the organization.

What You’ll Do

  • Lead, review, and approve deviation investigations and ensure timely resolution of quality events

  • Assess deviation impact, identify root causes, and support effective CAPA implementation

  • Manage change controls related to raw materials, supplier changes, and material lifecycle activities

  • Provide Quality Assurance oversight of Quality Control operations, laboratory systems, and analytical activities

  • Review and approve investigations related to OOS, OOT, atypical, and invalid laboratory results

  • Perform material disposition activities in accordance with approved procedures

  • Review and approve technology transfer protocols, reports, and technical documentation

  • Support internal audits, regulatory inspections, and third-party audits

  • Serve as a quality representative on cross-functional projects and continuous improvement initiatives

  • Provide technical guidance on GMP compliance, quality systems, and regulatory expectations

Who You Are

You are a collaborative quality professional who thrives in complex GMP environments and enjoys solving technical and compliance challenges. You are a proactive leader who can influence cross-functional teams, make risk-based decisions, and drive continuous improvement.

Required Skills

  • Bachelor's Degree plus minimum of 5 years of experience working in cGMP biotech or pharma quality positions

  • GMP and quality systems expertise

  • Demonstrated abilities in deviation investigation and root cause analysis

  • Experience with process validation or QC method/instrument validation

  • Change control management

  • Regulatory compliance knowledge (FDA, EMA, ANVISA)

  • Data integrity and laboratory systems knowledge

Preferred Skills

  • Experience supporting regulatory inspections and audits

  • Technology transfer experience

  • Experience with enrollment testing and release of raw materials

  • Quality Control experience


 

Job Level: Professional


Additional Information

The base compensation range for this role is: $93,000.00-$121,000.00


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.



Skills Required

  • Bachelor's Degree plus minimum of 5 years of experience working in cGMP biotech or pharma quality positions
  • GMP and quality systems expertise
  • Demonstrated abilities in deviation investigation and root cause analysis
  • Experience with process validation or QC method/instrument validation
  • Change control management
  • Regulatory compliance knowledge (FDA, EMA, ANVISA)
  • Data integrity and laboratory systems knowledge
  • Experience supporting regulatory inspections and audits
  • Technology transfer experience
  • Experience with enrollment testing and release of raw materials
  • Quality Control experience

Biogen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.

  • Fair & Transparent Compensation Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
  • Equity Value & Accessibility Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
  • Leave & Time Off Breadth Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.

Biogen Insights

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The Company
HQ: Cambridge, MA
9,575 Employees
Year Founded: 1978

What We Do

Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.

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