Senior Specialist, Technical Transfer – Small Molecules (m/f/d)

Merck Gruppe - MSD Sharp & Dohme; Unterschleißheim; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A global pharmaceutical company in Unterschleißheim is seeking a Senior Specialist (m/f/d) for Technical Transfer. The successful candidate will coordinate the transfer of sterile drug products and ensure compliance with technical and regulatory requirements. With 5+ years of experience in the pharma industry and expertise in GMP, this role offers a chance to impact a crucial investment project in a hybrid working environment.

Leistungen

Key role in strategic projects

Opportunity for career growth

Collaboration with global experts

Qualifikationen

• 5+ years of experience in technical transfer and manufacturing in the pharmaceutical industry.
• Familiarity with GMP and regulatory standards.
• Business-level English required; German preferred.

Aufgaben

• Coordinate technical transfers of sterile drug products.
• Act as a point of contact between global functions and the site.
• Monitor project timelines and deliverables.

Kenntnisse

Project Coordination

Technical Transfer

GMP Knowledge

Regulatory Compliance

Leadership

Adaptability

Ausbildung

Scientific or Technical Degree

Jobbeschreibung

Job Description

About the role

Our sterile Small Molecule site in Unterschleißheim is one of the key investment projects in our global manufacturing network.

To support the successful start-up of this facility, we are looking for a Senior Specialist (m/f/d), Technical Transfer – a hands-on expert who ensures that product transfers are executed efficiently, compliant, and on time.

In this role, you will coordinate and support the transfer of sterile drug products into our new site. You will act as a central interface between global functions (Quality, Regulatory, PTS) and local teams, making sure that technical, regulatory, and operational requirements align.

This position is part of the Small Molecules Technology Transfer Execution organization and will play a critical role in ensuring readiness for commercial operations.

Your Contribution

• Support and coordinate technical transfers of sterile Small Molecule drug products (process and analytical methods)
• Act as a key point of contact between global functions and the Unterschleißheim site
• Monitor and track project timelines, deliverables, and risks – using tools like dashboards and regular reporting
• Collaborate on submission packages and ensure alignment with Regulatory Affairs and Quality
• Work cross-functionally to ensure smooth handovers and successful implementation of product transfers
• Build strong working relationships with the local site team and understand the priorities and realities on the ground
• Escalate issues when needed – with confidence and clarity
• Bring a mindset of learning and flexibility – including potential exposure to product validation and PTS-driven projects

What You Bring

• A scientific or technical degree (e.g. in Chemistry, Pharmacy, Biology, Engineering or similar)
• 5+ years of experience in technical transfer, manufacturing, or technical operations in the pharmaceutical industry – preferably with sterile Small Molecule products
• Familiarity with GMP, regulatory standards, and pharma business processes (e.g. change control, deviations, protocols)
• Business-level English required; German preferred
• Strong project coordination skills – with the ability to keep track of multiple workstreams, deadlines and stakeholders
• A proactive, realistic and resilient mindset – you know when to raise your voice, when to listen, and when to push forward
• Experience working in cross-functional and international teams
• Readiness to travel (approx. 10-20%)

What we offer

• A key role in one of our company’s most important investment projects
• The opportunity to work in a newly built sterile facility and shape its operational success
• Collaboration with global experts and local site teams in a highly visible, cross-functional environment
• A culture that values technical excellence, responsibility, and continuous learning

Why This Role? Why Now?

This is a critical role in one of our most strategic investment projects – and a rare opportunity to shape the success of a new sterile manufacturing site from the ground up. Your work will directly impact product readiness, technical excellence, and the long-term success of the facility.

You’ll also gain exposure to global functions, diverse project teams, and cutting-edge operational setups – making this an ideal next step for someone looking to deepen their skills and grow their career within our company.

Interested in shaping something from the start?

Apply now and be part of a team that’s building more than a facility – we’re building the future of manufacturing.

Required Skills

Accountability, Accountability, Adaptability, Business Processes, Clinical Supply Chain Management, Clinical Trial Management, Feasibility Studies, Hardware Implementation, Leadership, Performance Monitoring, Pharmaceutical Management, Pharmaceutical Manufacturing, Pharmacy Regulation, Plan of Action and Milestones (POA&M), Process Improvements, Process Operations, Project Coordination, Project Planning, Quality Assurance (QA) Standards, Real World Evidence (RWE), Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Compliance, Risk Management, Self Motivation {+ 4 more}

Preferred Skills

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation

VISA Sponsorship

Travel Requirements

Hybrid

Flexible Work Arrangements

Hybrid

Shift

Valid Driving License

Hazardous Material(s)

Job Posting End Date

11/11/2025

A job posting is effective until 11:59:59PM on the day before the listed job posting end date. Please ensure you apply to a job posting no later than the day before the job posting end date.

Requisition ID

R371158