Quality Assurance Specialist, Commercial

Posted Yesterday
Be an Early Applicant
Basel, Basel-Stadt, CHE
In-Office
87K-108K Annually
Junior
Biotech
The Role
Executes commercial pharmaceutical quality assurance activities for externally manufactured APIs, drug products, and finished goods. Responsibilities include batch record review, data verification, batch disposition, quality system records, deviations, CAPAs, regulatory request support, inspection readiness, metrics tracking, and SOP maintenance. The role collaborates with CMOs and cross-functional stakeholders to support compliant, timely product release and commercial supply continuity within GMP-regulated environments.
Summary Generated by Built In

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The Quality Assurance Specialist, Commercial, executes Work Center Team (WCT) activities for externally manufactured commercial APIs, drug products, and finished goods. This role is responsible for batch record review, batch disposition, quality system execution, and regulatory activities that enable compliant, risk-based, and timely commercial product release across the global commercial supply network.

Essential Functions of the job:

  • Support multiple commercial products and CMOs while managing competing priorities in a fast-paced environment.

  • Perform batch record review and data verification for commercial APIs, drug products and finished goods manufactured at CMOs, in accordance with approved procedures.

  • Prioritize and execute batch review activities to support commercial supply commitments and product availability.

  • Perform batch disposition activities, including compilation, verification, and documentation of quality information supporting commercial product release.

  • Escalate quality or compliance observations identified during batch review in accordance with established procedures.

  • Initiate and manage quality system records (e.g., deviations, CAPAs) within the electronic Quality Management System (eQMS), including lifecycle tracking through closure.

  • Perform data verification and document completeness checks to support inspections, audits and regulatory requests.

  • Support regulatory request management, including document retrieval, archival and readiness for repeat requests.

  • Maintain trackers and metrics related to batch record review, record status and WCT deliverables.

  • Author, revise and maintain internal quality documents (i.e., SOPs, work instructions) as assigned.

  • Collaborate with CMO Managers and cross-functional stakeholders to support batch disposition, issue resolution and commercial supply continuity.

  • Perform other WCT responsibilities as assigned.

Education

  • Bachelor’s degree in scientific discipline or equivalent combination of education and 2+ years of work experience.

Required Experience

  • Experience in the pharmaceutical or biotechnology industry

  • Experience working in a GMP-regulated Quality function

  • Commercial Quality Assurance experience preferred

  • Previous experience navigating external manufacturing models would be an advantage

Knowledge, Skills, and Abilities

  • Strong understanding of GMP principles and pharmaceutical quality systems.

  • Working knowledge of pharmaceutical GMP requirements, including ICH Q7, ICH Q9, ICH Q10, 21 CFR Parts 210/211, EU GMP, and applicable global regulations.

  • Ability to support risk-based quality activities and quality system execution in accordance with established procedures and governance.

  • Ability to work independently in a regulated environment and manage competing priorities.

  • Strong analytical, problem-solving and organizational skills.

  • Excellent written, verbal and interpersonal communication skills.

  • High attention to detail and ability to collaborate cross-functionally.

Computer Skills

  • Proficiency in Microsoft Office applications (Outlook, Word, Excel, PowerPoint, Teams)

  • Experience with electronic Quality Management Systems (eQMS) required

Travel

  • Approximately 5 - 10% travel may be required

Salary Range Switzerland: 86,600.00 CHF - 108,200.00 CHF

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

Skills Required

  • Bachelor's degree in a scientific discipline or equivalent combination of education and 2+ years of work experience
  • Experience in the pharmaceutical or biotechnology industry
  • Experience working in a GMP-regulated Quality function
  • Commercial Quality Assurance experience
  • Previous experience navigating external manufacturing models
  • Strong understanding of GMP principles and pharmaceutical quality systems
  • Working knowledge of ICH Q7, ICH Q9, ICH Q10, 21 CFR Parts 210/211, EU GMP, and applicable global regulations
  • Ability to support risk-based quality activities and quality system execution
  • Ability to work independently in a regulated environment and manage competing priorities
  • Strong analytical, problem-solving, and organizational skills
  • Excellent written, verbal, and interpersonal communication skills
  • High attention to detail and ability to collaborate cross-functionally
  • Proficiency in Microsoft Office applications including Outlook, Word, Excel, PowerPoint, and Teams
  • Experience with electronic Quality Management Systems (eQMS)

BeiGene Compensation & Benefits Highlights

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

  • Equity Value & Accessibility Equity grants and stock programs are widely available across roles, including RSU grants at hire and opportunities to participate in company equity plans. Total compensation commonly includes equity alongside base pay and incentives.
  • Healthcare Strength Health coverage is described as comprehensive and high quality, with multiple mentions of “top notch” medical benefits. This strength is consistently highlighted as a key component of the package.
  • Retirement Support Retirement offerings include a 401(k) with a competitive employer match. These features contribute to a strong overall compensation bundle.

BeiGene Insights

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The Company
HQ: Cambridge, MA
2,862 Employees
Year Founded: 2010

What We Do

BeiGene is a global biotechnology company that is developing and commercializing innovative and affordable oncology medicines to improve treatment outcomes and access for far more patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 8,500 colleagues spans five continents, with administrative offices in Beijing, China; Cambridge, U.S.; and Basel, Switzerland. To learn more about BeiGene, please visit www.beigene.com and follow us on Twitter at @BeiGeneGlobal. See our community guidelines: bit.ly/39o3O6j

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