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Project Manager GMP & Quality Operations (mfd) Global Quality Operations

Merz Therapeutics


Job Location:

Frankfurt am Main - Germany

Monthly Salary: Not provided by the employer
Posted: 3 September 2026 (11 days ago)
Application Deadline: 1 December 2026
Vacancies: 1 Vacancy

Job Summary

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 needsinvesting 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


Required Experience:

IC


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