Project Manager GMP & Quality Operations (m/f/d) Global Quality Operations

Merz Therapeutics; Frankfurt; Vor Ort; EUR 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Hybrid work model

Attractive remuneration with social

WellPass/Deutschland-Ticket/Corporate-

JobBike

Company restaurant

Zusammenfassung

Merz Therapeutics in Germany seeks a Project Manager GMP & Quality Operations to drive cross-functional, GMP-relevant projects within Global Quality Operations. You will coordinate infrastructure, quality, and process-improvement initiatives, delivering on time and within budget over a 24-month fixed-term contract.

The role requires 5+ years in pharma (Quality/Operations/PM), GMP/GDP expertise, and strong communication. English fluent; German a plus.

Qualifikationen

• Degree in a scientific field (pharmacy, chemistry, biology, biotech, engineering)
• Min. 5 years in pharma, ideally Quality/Operations/PM
• Experience with GMP-regulated infrastructure, lab, transfer projects
• Strong knowledge of GMP/GDP, quality systems, change control, qualification, validation
• PMI, PRINCE2 or similar certification is an advantage
• Strong analytical thinking; ability to manage complex topics
• Excellent communication and stakeholder management with hands-on mindset
• Business fluent in English; German is a plus

Aufgaben

• Manage cross-functional quality and compliance projects, timelines, budgets, and quality targets
• Coordinate setup of a new GMP laboratory incl. infrastructure and facilities
• Lead equipment transfer, qualification, and requalification with key stakeholders
• Coordinate internal and external stakeholders incl. suppliers, service providers, and contract manufacturers
• Support change control activities and risk assessments related to quality, compliance, and patient safety
• Coordinate quality-related implementation of regulatory packaging material requirements and monitor progress
• Maintain project plans, risk assessments, status reports, and audit-ready documentation
• Support process implementation and handover to operational quality teams

Kenntnisse

Project management

GMP/GDP knowledge

Stakeholder management

Analytical thinking

Communication

English proficiency

German language (plus)

Ausbildung

Degree in Pharmacy, Chemistry, Biology, Biotechnology, Engineering or related field

Tools

PMI/PRINCE2 certification

Jobbeschreibung

YOUR CONTRIBUTION

As Project Manager GMP & Quality Operations (m/f/d), you will play a key role in driving complex cross-functional projects within Global Quality Operations. You will ensure that strategic, GMP-relevant, and compliance-critical initiatives are delivered on time, within budget, and according to quality requirements. Acting as a central coordinator, you will collaborate with internal and external stakeholders to successfully implement infrastructure, quality, and process improvement projects. This position is offered as a fixed-term contract for 24 months.

Your responsibilities will include the following tasks:

• Manage cross-functional quality and compliance projects, ensuring timelines, budgets, and quality targets are met
• Coordinate the setup of a new GMP laboratory, including infrastructure, equipment, and technical facilities
• Drive equipment transfer, qualification, and requalification activities with key stakeholders
• Coordinate internal and external stakeholders, including suppliers, service providers, and contract manufacturers
• Support change control activities and risk assessments related to quality, compliance, and patient safety
• Coordinate quality-related implementation of new regulatory packaging material requirements and monitor progress
• Maintain project plans, risk assessments, status reports, and audit-ready documentation
• Support process implementation and ensure effective handover to operational quality teams

YOUR PROFILE

• Degree in Pharmacy, Chemistry, Biology, Biotechnology, Engineering, or a related scientific field
• Min. 5 years of experience in the pharmaceutical industry, ideally in Quality, Operations, or Project Management
• Experience managing GMP-regulated infrastructure, laboratory, qualification, or equipment transfer projects
• Strong knowledge of GMP/GDP requirements, quality systems, change control, qualification, and validation
• Excellent project management skills; PMI, PRINCE2, or similar certification is an advantage
• Strong analytical thinking and ability to manage complex technical and regulatory topics
• Excellent communication, stakeholder management, and organizational skills with a hands-on mindset
• Business fluent in English; German language skills are a plus

YOUR BENEFITS

• Individual career development in a purposeful job: you improve the quality of life of our patients!
• Global family business with flat hierarchies and an open, respectful corporate culture
• Hybrid work model that allows a good work-life balance
• Attractive location with good transport links, modern workplaces and a company restaurant
• Attractive remuneration with extensive social benefits
• Variety of employer-subsidized benefits such as WellPass, Deutschland-Ticket, Corporate Benefits and JobBike

Find out more about our benefits here.

ABOUT US

Welcome to Merz Therapeutics, a global leader in specialty neurology, delivering innovative treatments that help people with movement disorders, neurodegenerative conditions, liver disease, and other serious health challenges regain their quality of life.

We are proud to be a family-owned company with over 117 years of heritage. Our therapies reach patients in more than 80 countries, driven by a passion for innovation and a commitment to growth.

Our goal is to address urgent, unmet medical needs-investing in research, expanding our portfolio, and empowering people to live better lives.

Join our international Merz Therapeutics family and help us achieve our mission:

"BETTER OUTCOMES FOR MORE PATIENTS"