Sr. Associate III, Quality Control

Reposted 2 Days Ago
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Baar, Zug, CHE
In-Office
Senior level
Biotech
The Role
Lead management of external testing and contract laboratories to ensure timely, compliant product release. Oversee project delivery, budgets, PO creation, spend tracking, and audit-ready documentation. Drive process improvements, risk management, and strategic testing decisions. Mentor team members, coordinate cross-functional stakeholders, escalate compliance gaps, and represent quality control with senior management and external partners.
Summary Generated by Built In

About This Role: 

As the Sr. Associate III for Quality Control within the Global External Testing Management team, you will play a crucial role in ensuring the timely and compliant release of our products. You will be responsible for overseeing all aspects of testing conducted at contract laboratories, which support both internal and external manufacturing processes. Your strategic leadership will be essential in managing financial planning, contract management, and driving process innovations that balance cost with value, aligning with our Vision 2030 objectives. In this role, you will have the opportunity to influence cross-functional operations, make decisive testing strategy decisions, and effectively communicate risks impacting product release and compliance. This position serves as a vital component in our business structure, contributing to the overall success and efficiency of our quality control operations.

What You'll Do:

  • Develop, implement, and manage multiple quality control projects supporting contract laboratory management and product testing.
  • Communicate and manage external testing and project status, spending, and direction with stakeholders.
  • Identify and implement process improvements to enhance efficiency, compliance, and communication across contract laboratory operations.
  • Ensure robust information management and documentation practices to support audit readiness and regulatory compliance.
  • Manage financial aspects of external testing, including purchase order creation, spend tracking, and budgeting/budget reforecasting.
  • Lead and oversee key site/global projects while providing mentorship to team members.
  • Influence and coordinate with cross-functional teams to achieve departmental objectives.
  • Escalate risks and compliance gaps to senior management effectively.
  • Provide strategic technical leadership and drive program acceleration with risk/cost management.
  • Represent quality control in interactions with senior management and external stakeholders.
  • Maintain a thorough understanding of impact and mitigation for project teams and quality directives.

Who You Are: 

You are a strategic thinker with a deep understanding of quality control processes and compliance requirements. Your ability to communicate effectively and escalate risks will set you apart in this role. You thrive in ambiguous situations and have a knack for guiding experimental approaches. Your leadership skills enable you to mentor others, driving the team towards achieving departmental objectives. You are detail-oriented yet able to see the big picture, balancing cost with value in strategic decision-making.

Required Skills:

  • B.S or M.S. degree (preferably in Life Science and management).
  • At least 7 years of relevant experience in pharmaceutical or biotech manufacturing environment.
  • Experience with regulatory audits, quality systems, business processes, and project management.
  • Strong risk management skills and ability to develop measurable improvements.
  • Effective communication and leadership competencies.
  • Proven ability to manage complex problems and mentor others effectively.

Preferred Skills:

  • Experience in financial planning and contract management.
  • Familiarity with Vision 2030 objectives and strategic work relationships.
  • Background in managing external testing operations and process innovation.


 

Job Level: Management
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 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

  • B.S. or M.S. degree (preferably in Life Science or management)
  • At least 7 years relevant experience in pharmaceutical or biotech manufacturing environment
  • Experience with regulatory audits, quality systems, business processes, and project management
  • Strong risk management skills and ability to develop measurable improvements
  • Effective communication and leadership competencies
  • Proven ability to manage complex problems and mentor others effectively
  • Experience in financial planning and contract management
  • Familiarity with Vision 2030 objectives and strategic work relationships
  • Background in managing external testing operations and process innovation

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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