Associate Director, GCP Inspection Office, R&D Quality

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. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

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

R&D Quality encompasses four teams GCLP/GLP Quality, PV Quality, Audit Calibration, Quality and GCP Quality. R&D Quality has a large range of stakeholders, and we have an important role in delivering our 2030 vision to transform the future of cancer treatment.

In the role as AD GCP Inspection Office you will be driving day-to-day GCP Quality activities including audit together with a dedicated and highly skilled team. Furthermore, you will be taking up the role as GCP Inspection QA lead.

The role requires profound understanding of how the GCP requirements are applied into practice, especially with focus on the European requirements and interpretation of ICH GCP R3 and Computerized Systems in Clinical Trials.

The role includes hands on GCP Quality activities such as support to our many stakeholders as well as performing audits alone or together with own team members or with support from neighbouring teams. You become a key member of the R&D Quality leadership team that together drives people engagement, setting strategies and ensuring R&D Quality deliverables.

The role requires strong collaboration capabilities in an international setting across various QA departments as well across the company with target stakeholders such as Clinical Trial Operations, Clinical Data, Integration & Reporting, Digital Development, Medical, GDS&PV, and Regulatory Affairs.

Key Responsibilities

• Develop and maintain the GCP Quality strategies in collaboration with the R&D Quality leadership team
• Foster communication with relevant stakeholders and the teams within R&D Quality
• Ensure that GCP compliance in alignment with Genmab's Quality Policy, procedures and regulatory requirements
• Maintain a risk-based approach for conducting trial site audits, process audits and audits of service providers
• Develop and execute the annual GCP audit plan in partnership with GCLP/GLP Quality and Audit Calibration.
• Oversee and coordinate regulatory GCP inspections, including pre-inspection preparation and post inspection follow ups.
• Drive standardization, harmonization, and scalability of GCP Quality processes
• Ensure compliance with global GxP standards, regulatory requirements, and Genmab Quality Systems
• Lead quality improvement initiatives to enhance processes and procedures.
• Review and contribution to Standard Operating Procedures (SOPs) and approve QMS doc

Requirements

• MS, or BS or similar in Natural Science
• 10+ years of experience in a GCP Quality function or similar
• Deep expertise in GCP processes and the EMA, PMDA and FDA requirements.
• Demonstrated leadership in regulatory inspections and health authority interactions.
• Considered to be a Domain Expert within GCP by peers with a strong interest and ability to educate others
• Experience as Lead Auditor within GCP is an advantage

For US based candidates, the proposed salary band for this position is as follows:

$156,000.00---$234,000.00

The actual salary offer will carefully consider a wide range of factors, including your skills, qualifications, experience, and location. Also, certain positions are eligible for additional forms of compensation, such as discretionary bonuses and long-term incentives.

When you join Genmab, you're joining a culture that supports your physical, financial, social, and emotional wellness. Within the first year, regular full-time U.S. employees are eligible for:

• 401(k) Plan: 100% match on the first 6% of contributions
• Health Benefits: Two medical plan options (including HDHP with HSA), dental, and vision insurance
• Voluntary Plans: Critical illness, accident, and hospital indemnity insurance
• Time Off: Paid vacation, sick leave, holidays, and 12 weeks of discretionary paid parental leave
• Support Resources: Access to child and adult backup care, family support programs, financial wellness tools, and emotional well-being support
• Additional Perks: Commuter benefits, tuition reimbursement, and a Lifestyle Spending Account for wellness and personal expenses

Further details on eligibility for compensation and benefits based on role 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 Job Applicant Privacy Notice (genmab.com) .

Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.