Head of MSAT Process Science Marburg (m/f/d)

Heute
Marburg an der Lahn
Vollzeit
Geschätztes Gehalt

Das könntest du laut kununu User:innen als Leiter:in Prozessmanagement in Deutschland verdienen

Ø 90.600 €
Bruttodurchschnittsgehalt Vollzeit
55.500 €147.100 €
Was die Firma über den Job sagt

Head of MSAT Process Science Marburg (m/f/d)

Business Introduction

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.

Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.

We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary

As Head of MSAT Process Science, you will lead the MSAT Process Science laboratories in Marburg. You will provide scientific and people leadership, support manufacturing operations, drive proactive process improvements through laboratory studies, and investigate and resolve complex manufacturing challenges.

You will strengthen Process Science capabilities across four pillars: process knowledge; people competency and capacity; laboratory infrastructure; and internal and external networking capability. You will ensure that laboratory priorities, resources and capabilities remain aligned with product and platform portfolio needs.

In this role, your key responsibilities will include:

  • Fulfil the employer’s occupational health and safety duties for MSAT Process Science, including preventing work-related accidents and diseases and implementing necessary health measures.
  • Provide long-term strategic direction and technical input to Manufacturing Support Teams, local MSAT communities and Molecule Steward groups to support product lifecycle decisions across the relevant portfolio, including viral vaccines such as measles, mumps and rubella, recombinant proteins for Bexsero, and conjugate vaccines.
  • Ensure technical and scientific support for commercial manufacturing technology transfers, including comprehensive product technical assessments and the sharing of data, product knowledge and process expertise.
  • Lead technical and laboratory resources to deliver product-related projects and changes.
  • Lead, coach and develop a multidisciplinary laboratory team; establish clear objectives, succession and capability plans, and an inclusive, accountable culture.
  • Own laboratory strategy, capacity planning, resource prioritization and budget stewardship, including equipment lifecycle, maintenance, qualification and future capability investments.
  • Ensure laboratory activities, methods, documentation, data and computerized systems comply with applicable GLP, data integrity, quality and regulatory requirements.
  • Oversee scientifically rigorous study design, execution, interpretation and reporting, applying risk assessment, design of experiments, statistical analysis and process modelling where appropriate.
  • Provide technical leadership on governance committees and decision-making bodies.
  • Manage the portfolio of manufacturing technologies and innovations.
  • Provide technical oversight and leadership for manufacturing operations, commercial contract manufacturing organizations (CMOs) and manufacturing partners to help achieve business objectives.
  • Develop and govern harmonized business processes and tools for technical manufacturing support, technology transfer, product lifecycle management and innovation management.
  • Build effective technical relationships across Manufacturing, Quality, Regulatory, R&D, Engineering, Digital/Data, other MSAT teams, external partners and sites.
  • Ensure appropriate GSP, housekeeping and safety standards within your areas of responsibility, in accordance with company requirements and applicable national and international regulations.

Additional information

  • Reporting line: Biologics Platform Technologies Head
  • Position level: Director
  • People management: approximately 16 direct reports
  • Primary location: Marburg Main Site (Germany)
  • Secondary location: N/A
  • Working arrangement: hybrid
  • Business travel: limited
  • Languages: fluent German and English, spoken and written

Why You?

Basic Qualifications

We are looking for professionals with the following skills and qualifications:

  • MSc, preferably in science, engineering or pharmaceutical technology, or equivalent experience
  • Substantial experience in pharmaceutical or biopharmaceutical R&D, Process Development, MSAT or commercial manufacturing in a regulated environment
  • Demonstrated experience leading process-science or laboratory teams and delivering through cross-functional and matrix organizations
  • Strong operational leadership, people development, resource prioritization and stakeholder-influence experience at senior level
  • Strong scientific knowledge of vaccine manufacturing, process characterization, analytical testing, technology transfer, validation and product lifecycle management
  • Experience applying risk management, root-cause analysis, design of experiments, process modelling and statistics to manufacturing and laboratory challenges
  • Experience with statistical and data-analysis software; coding experience in Python, C++ or similar tools is an advantage
  • Understanding of complex transformation and change management projects
  • Ability to navigate ambiguity and apply an agile mindset in a complex site environment
  • Digital fluency, with a strong understanding of data integrity and the use of digital tools in a regulated laboratory environment
  • Fluency in German and English, spoken and written (mandatory requirement)

Preferred Qualifications

The following qualifications and attributes would be an advantage:

  • PhD in pharmacy, pharmaceutical technology, chemical or biochemical engineering, chemistry, life sciences, or a related discipline
  • Significant experience leading a GMP laboratory, process-science function or comparable technical organization, ideally supporting vaccines or biologics
  • Ability to influence a wide range of stakeholders, communicate clearly and demonstrate resilience
  • A proactive, agile and independent approach, with a strong focus on delivering results
  • Ability to offer objective perspectives and practical solutions to challenges across functions and business areas
  • Excellent interpersonal and communication skills.

What you will bring

You will bring scientific expertise, a collaborative leadership approach and a commitment to safe, high-quality manufacturing. You will connect teams across sites, translate process knowledge into practical improvements and strengthen the capabilities needed to support reliable product supply.

How to apply

Please submit your CV and a short note explaining how your experience aligns with the responsibilities and qualifications for this role. We welcome applicants from all backgrounds and encourage people who value inclusion and teamwork to apply. We look forward to hearing from you.

Application end date

Sunday, 6 December 2026, end of day CET

#LI-GSK

Skills

Digital Fluency, German Language, Manufacturing Processes, Manufacturing Production, Manufacturing Technologies, People Leadership, People Management, Research and Development, Technology Transfer

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at DE.Contact-Recruitment@gsk.com where you can also request a call.

Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to ethnicity, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

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