Senior Manager, QA Commercial - Chemical Intermediates

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

The Role

The role is a senior quality manager responsible for GMP quality oversight of commercial Chemical Intermediates (CI) manufactured at external Contract Manufacturing Organizations (CMOs). The role is based in Denmark and reports to the Director responsible for QA Commercial - Head of Drug Substance & Intermediate.

You will be part of an experienced and highly skilled QA organization, with this position holding primary accountability for Chemical Intermediates, while working closely with colleagues responsible for Biologic Intermediates (BI) and Drug Substance (DS) to ensure aligned quality governance across commercial supply chains. The role interfaces extensively with CMOs, partners, and internal subject matter experts across Quality, Regulatory Affairs, Technical Operations, and Supply Chain.

Key Responsibilities

General Compliance

• Lead QA representation for Chemical Intermediate supply chains in cross-functional Genmab project groups and key external collaborations, providing expert input and ensuring alignment with QA governance and regulatory expectations.
• Act as a QA subject matter expert on GMP for Chemical Intermediates, including small-molecule intermediates and related manufacturing activities, providing expert guidance and supporting resolution of complex quality issues.
• Gain and maintain expert knowledge of applicable GMP legislation, guidelines, and industry practices relevant to Chemical Intermediate manufacturing; assess applicability to Genmab activities and ensure structured dissemination of relevant updates to stakeholders.
• Lead the resolution of CI-related quality issues in collaboration with internal and external stakeholders, escalating critical or high-risk matters as appropriate to ensure timely and compliant decision-making

Pharmaceutical Quality System (PQS)

• Continuously improving PQS: Participate in developing, maintaining, and continuously improving Genmab's Pharmaceutical Quality System (PQS) in alignment with applicable GMP and GDP requirements.
• Quality Risk Management: Apply and support quality risk management principles in complex PQS activities, providing expert input to risk assessments and mitigation actions.
• Procedures: Review/authoring and approval of SOPs, Work Instructions, templates and forms within assigned areas, and support document updates in accordance with the PQS.
• Deviation, CAPA, Change Control: Handle and support deviations, CAPAs and change controls, providing expert input and ensuring compliance with procedures and applicable regulatory requirements.
• Inspections & Audits: Participate in audits and inspections performed by national authorities and internal or external auditors as required. Support audit and inspection readiness by ensuring documentation, procedures and processes within assigned scope are maintained in compliance with company standards and applicable regulations. Support audit and inspection preparation and conduct through back-office activities, documentation and presentation support.
• QMR: Provide expert input to Quality Management Reviews (QMRs) as part of the PQS, contributing to data analysis, trend interpretation and identification of quality risks and improvement opportunities.
• Complaints & Recalls: Handle and support complex product complaints and recall-related activities as part of the PQS, providing expert input to investigations, risk assessments and corrective actions in compliance with procedures and regulatory requirements.
• Batch Review & Release: Perform batch review and batch release activities and act as delegated QP and ensure compliance with approved procedures and regulatory requirements.
• CPV: Support, review and approve Continued Process Verification (CPV) activities as part of the PQS, providing expert input to data analysis, trend evaluation and identification of potential process risks in compliance with regulatory requirements.
• APQR: Prepare, review and support complex Annual Product Quality Reviews (APQRs) as part of the PQS, providing expert input to data analysis, trend evaluation and conclusions in compliance with regulatory requirements.
• Training: Provide expert training in complex or specialized quality topics as defined by QA, supporting consistent understanding and application of quality requirements.

Supplier Quality Oversight

• Provide expert and operational supplier quality oversight for Chemical Intermediate manufacturers and relevant raw material suppliers, including supplier audits, supplier risk evaluations, Quality Agreements, supplier meetings, and external notifications.
• Provide expert input to the resolution of complex CI-related supplier quality issues, ensuring compliance with regulatory requirements and Genmab quality standards.

Requirements

• Bachelor's or Master's degree (or equivalent) in a relevant life science discipline.
• Solid experience (5 years) within pharmaceutical QA GMP, Related to Chemical Intermediates.
• Experience with outsourced manufacturing.
• Strong communication and collaboration skills; fluent in English.
• Ability to work independently in a complex and fast-paced environment.
• Ability to thrive in a fast-paced and changing environment
• Results-oriented and committed to contributing to Genmab's overall success

The proposed gross annual base salary range for this position, in the primary location, based on a full time schedule is:
DKK607.920,00---911.880,00

The final salary offer will depend on several factors, including your skills, qualifications, and experience.

In addition to base salary, this position is eligible to additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you become a part of a culture that supports your physical, financial, social, and emotional well-being. Our benefits include, but are not limited to:

• Pension
• Health insurance and wellness benefits
• Paid time off
• Employee support programs

Further details on compensation and benefits will be provided during the recruitment process.

About Genmab

Genmab is an international biotechnology company with a core purpose to improve the lives of patients through innovative and differentiated antibody therapeutics. For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. By 2030, Genmab's vision is to transform the lives of people with cancer and other serious diseases with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Established in 1999, Genmab is headquartered in Copenhagen, Denmark with international presence across North America, Europe and Asia Pacific. For more information, please visit Genmab.com and follow us on LinkedIn and X.

Genmab is committed to protecting your personal data and privacy. Please see our privacy policy for handling your data in connection with your application on our website

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