Senior Associate Project Manager CMC Product Lifecycle Management

Genmab; København; In loco; DKK 507.000 - 760.000; Tempo pieno

Vantaggi offerti da questo lavoro

Pension

Health insurance and wellness benefits

Paid time off

Employee support programs

Descrizione del lavoro

Genmab is seeking an Associate Project Manager to join the CMC Life Cycle Management team in Denmark. You will provide operational coordination to Project Managers and Directors, supporting post-launch lifecycle activities and manufacturing oversight across CMOs and internal partners.

The role focuses on maintaining plans, records, and timely communications, in a regulated environment, with opportunities to impact product lifecycle management and quality processes.

Competenze

• Master’s degree in science or related field required.
• 2+ years in TechOps or related biopharma area in a regulated setting.
• Experience supporting project activities for commercial products.
• Fluent in English and able to communicate across cultures.

Mansioni

• Support manufacturing and lifecycle plans with schedules and trackers.
• Coordinate meetings, prepare materials, and track actions across teams.
• Monitor deviations, changes, complaints, and batch release activities.
• Maintain records in GXP systems and assist regulatory submissions as needed.
• Identify risks and improvements; assist in SOP and process updates.

Conoscenze

Masters in science

TechOps experience

Project coordination

English fluency

Organizational skills

Formazione

Master’s degree in science

Strumenti

QMS systems

Descrizione del lavoro

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?

At Genmab, we are committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people who are caring, candid, and impact-driven to our business, which is innovative and rooted in science, we believe that being proudly unique, determined to be our best, and authentic is essential to fulfilling our purpose.

The Role and Department

Genmab is seeking an Associate Project Manager to join the CMC Life Cycle Management (LCM) team and provide operational coordination and administrative support to Project Managers, Senior Project Managers and Associate Directors managing our commercial product portfolio.

The LCM team supports post-launch CMC lifecycle activities and manufacturing oversight. You will help keep plans, actions and documentation current, working with Commercial Supply Chain, MSAT, Regulatory CMC, Commercial QA, External Manufacturing and CMOs.

The team is part of CMC Project and Portfolio Management within CMC Development and Manufacturing, based in Denmark.

Application deadline: 1. November 2026

Key Responsibilities

• Support execution of manufacturing and lifecycle plans by maintaining schedules, milestone trackers and task lists, following up on deliverables and flagging delays to accountable LCM leads
• Coordinate meetings and routine communication across project teams, CMOs and stakeholders; prepare agendas and materials, record decisions and actions, and follow up with action owners
• Support daily operations by tracking assigned LCM activities relating to deviations, changes, complaints, batch release and supply
• Coordinate information and follow-up with responsible functions. Update and maintain necessary records in the associated GXP systems
• Provide support for lifecycle regulatory documentation and submissions as needed by collecting information, organizing records and tracking review deadlines under guidance from LCM colleagues
• Follow Genmab quality system requirements and develop an understanding of CMO/Partner quality agreements and their quality and technical implications
• Identify risks, missing information and overdue actions; maintain risk and issue logs and elevate concerns promptly to the accountable LCM responsible
• Identify improvement opportunities and support updates to tools, templates, documentation processes and LCM ways of working
• Support development of associated SOPs, working instructions and other relevant documents to support LCM ways of working and product lifecycle management

Requirements

• Master’s degree in science or a related technical discipline, such as engineering, biotechnology, pharmaceutical sciences, biochemistry or biology, or equivalent experience
• 2+ years of experience in TechOps or a related area in biopharma, biotechnology, medical devices or another relevant industry, or an equivalent combination of education and experience
• Hands‑on experience supporting project activities or operations activities for products in commercial phase and managing tasks in a structured, regulated environment; familiarity with document management tools and QMS systems
• Basic understanding of pharmaceutical regulations and quality requirements, with willingness to develop knowledge of commercial manufacturing and CMO collaboration
• Some experience building relationships and stakeholder management; clear communication skills and fluency in English.
• Strong organizational skills; ability to prioritize assigned tasks and collaborate across functions and cultures

The proposed gross annual/hourly base salary range for this position, in the primary location, based on a full time schedule is:

DKK506.532,00---759.798,00

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

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

Benefits

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 eligibility for compensation and benefits based on the 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.

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