18 beste Stellen als validation expert in bayern – aktuell auf Personalsuche

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GES Process Lead (f/m/d) (MUSE) - Associate Director

MSD -
Unterschleißheim

Jetzt bewerben

Details zur Stelle

Vollzeit
vor 2 Tagen

Qualifikationen

Bachelor
Projektleitung
Führungserfahrung

Vollständige Stellenbeschreibung

Job Description

Shape the Future of Pharmaceutical Manufacturing

As GES Process Lead (f/m/d), you will provide end-to-end leadership for process engineering and manufacturing design across a major capital project. From early concept development through detailed design, commissioning, qualification, and operational handover, you will ensure that manufacturing systems are safe, compliant, scalable, and ready to deliver for patients.

This role combines technical expertise, project leadership, and stakeholder management. You will work at the intersection of Engineering, Operations, Quality, Automation, and Science Technology, driving critical decisions that influence project success, operational readiness, and long-term business performance.

Primary Responsibilities

Lead process engineering activities from concept design through startup and handover to Operations.
Translate manufacturing requirements into robust process and equipment designs that meet safety, quality, compliance, and operational objectives.
Own key process engineering deliverables, including process design documentation, equipment specifications, process risk assessments, and control strategies.
Drive cross-functional collaboration across Engineering, Operations, Quality, CQV, Automation, and external partners.
Ensure compliance with GMP requirements, company standards, engineering best practices, and regulatory expectations.
Lead technical reviews, risk assessments, and design decisions to support project execution and operational readiness.
Guide process equipment selection, implementation, commissioning, qualification, and startup activities.
Provide leadership to Suite Leads and Process Package Owners, ensuring alignment across project workstreams.
Support governance, issue resolution, escalation management, project schedule adherence, and sustainable knowledge transfer to site operations.

Required Experience Skills

Bachelors degree in Chemical Engineering, Biotechnology, Pharmaceutical Engineering, or a related field.
Extensive experience in pharmaceutical, biotech, vaccine, or other highly regulated manufacturing environments.
Demonstrated success leading process engineering workstreams on complex capital projects.
Strong understanding of GMP, process design, commissioning, qualification, and validation principles.
Experience driving decisions and delivering results in large, cross-functional project teams.
Excellent communication, stakeholder management, and leadership skills.
Ability to navigate complexity, influence across functions, and maintain focus on business outcomes.

What We Offer

Youll have the opportunity to lead high-impact projects that enable the delivery of innovative medicines and vaccines to patients worldwide. Working with global teams and industry-leading experts, youll help shape next-generation manufacturing capabilities while expanding your own leadership and technical expertise.

We are proud to be an equal opportunity employer and are committed to fostering an inclusive and diverse workplace.

Required Skills:
Adaptability, Adaptability, Asset Management, Chemical Engineering, Cross-Functional Collaboration, Customer-Focused, Data-Driven Decision Making, Drug Product Development, Engineering Processes, Engineering Standards, Equipment Sizing, Estimation and Planning, GMP Compliance, Manufacturing Quality Control, Manufacturing Strategies, Pharmaceutical Process Development, Phenomenology, Process Architecture, Process Control Automation, Process Engineering, Process Optimization, Process Technologies, Product Formulation, Project Delivery, Safety Compliance {+ 2 more}

Preferred Skills:
Current Employees applyHERE

Current Contingent Workers applyHERE

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:
No relocation

VISA Sponsorship:
No

Travel Requirements:
25%

Flexible Work Arrangements:
Not Applicable

Shift:
Not Indicated

Valid Driving License:
No

Hazardous Material(s):
n/a

Job Posting End Date:
07/27/2026*A job posting is effective until 11:59:59PM on the dayBEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFORE the job posting end date.
Requisition ID: R406637

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validation expert Jobs in bayern

GES Process Lead (f/m/d) (MUSE) - Associate Director

Solution Architect - Implementation Lead

Principal System Engineer (f/m/d)

Entwicklungsingenieur E/E (w/m/d)

Principal Analog Engineer - Intelligent Power Devices

Product Owner - VDC Manager (f/m/d)

Sachbearbeiter - Rechnungswesen Rechnungsbearbeitung / SAP VIM (all genders) in Teilzeit

Working Student Software Engineering Python (all genders)

Functional Safety Architect (f/m/d)

Embedded Systems Working Student

Senior Embedded Software Developer (C) (f/m/d)

Werkstudent*in (w/m/d) Clinical Insights for AI in Medical Imaging

Working Student Software Engineering Python (all genders)

Senior Hardware Design Engineer (f/m/d)

Flight Control Engineer (m/f/d)

Principal Technical Leader for Automotive Systems Power

Flight Control Engineer (Modelling and System Identification) (m/f/d)

Quantum Software Engineer, Benchmarking and Error Reduction

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