20 beste vacatures voor de functie van regulatory, permitting & solutioning in utrecht leidsche rijn (nieuwe medewerkers gezocht)

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Scientist, Mass Spectrometry Characterization

Genmab -
Utrecht

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Vacaturegegevens

€ 58.000 - € 87.000 per jaar
13 dagen geleden

Kwalificaties

Doctor
Projectcoördinatie
Master
Analytisch vermogen
Leidinggevende ervaring
Begeleiding
Scheikunde

Volledige vacaturetekst

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

As a Scientist Mass Spectrometry within the Structural Characterization group of the Analytical Development department, you will contribute to the analytical characterization of our antibody-based therapeutics, helping to generate the data and scientific insights that support their progression from development through to regulatory submission and beyond. While you will contribute across the product lifecycle, your primary focus will be on early-stage CMC development and regulatory filings.

In this entry-level Scientist role, you will design, coordinate, interpret, and communicate mass spectrometry-based characterization studies using state-of-the-art instrumentation. You will combine hands-on scientific expertise with project coordination and will provide day-to-day guidance to a small team of Research Associates, helping them grow while ensuring high-quality execution.

Working closely with colleagues across Analytical Development and CMC, you will ensure that studies are scientifically robust, regulatory relevant, and delivered with a strong focus on data integrity. You will also have the opportunity to contribute to the continuous development of our mass spectrometry capabilities, helping shape how we characterize the next generation of antibody therapeutics.

Does this sound like you? We encourage you to apply by submitting your CV and motivation letter. We look forward to learning more about you and your experience!

Responsibilities

Manage, coach, and support a small group of Research Associates, including day-to-day prioritization, scientific guidance, feedback, and development.

Plan, coordinate, and provide scientific oversight for mass spectrometry-based characterization studies of antibody-based therapeutics across early- and late-stage CMC projects.

Guide the design, optimization, troubleshooting, and implementation of LC-MS/MS-based analytical workflows, including peptide mapping, intact and reduced mass analysis, and other protein characterization approaches.

Interpret complex analytical data and translate findings into clear conclusions, recommendations, technical reports, and regulatory-supporting documentation.

Collaborate with internal and external stakeholders to support product understanding, comparability, process development, formulation development, and regulatory filings.

Contribute to continuous improvement of mass spectrometry workflows by identifying opportunities to strengthen robustness, efficiency, data quality, and scientific relevance.

Requirements

A PhD in a relevant scientific discipline, or an MSc with approximately three to five years of relevant experience in mass spectrometry-based analytics.

Strong understanding of LC-MS/MS, protein chemistry, peptide mapping, intact and reduced mass analysis, chromatography, and mass spectrometry data interpretation.

Experience with analytical characterization of therapeutic proteins, preferably antibody-based products, in a CMC or biologics development environment.

Experience with coaching, mentoring, supervising, or coordinating the work of others is preferred.

Ability to manage multiple priorities, communicate clearly, and deliver high-quality scientific output within agreed timelines.

Motivated by working in a collaborative environment, supporting the development of others, and continuously improving analytical workflows.

Intended Recruitment Timeline

Application deadline: Thursday 13 August (end of day).
Shortlisting: week of 17 August.
Virtual screenings: weeks of 24 August.
Onsite interviews: first two weeks of September.
Intended start date: 1 Oct / 1 Nov.

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

EUR58.000,00-87.000,00


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.

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.

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 contract.

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regulatory, permitting & solutioning vacatures in utrecht leidsche rijn

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Director, Global Drug Safety & Pharmacovigilance Physician

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Consultant – Climate Change Advisory

Clinical Research Associate

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Director, Global Regulatory Affairs, Strategy

Junior Consultant Site Investigation and Remediation - Netherlands

Regulatory Compliance Specialist

IAM Expert

Senior QA Officer

Senior Environment & Regulatory Affairs Advisor

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Global Land Logistics Expert

Senior Compliance Officer

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory, permitting & solutioning in utrecht leidsche rijn

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