GMP Project Manager - Pharma (80 - 100%)

Eurofins Germany BioPharma Product Testing; Konstanz; Hybrid; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading biopharmaceutical outsourcing partner in Germany is looking for a GMP Project Manager Pharma. This role involves end-to-end project leadership in Pharma Analytics, ensuring compliance with GMP standards and managing project timelines. The ideal candidate will hold a degree in life sciences and have at least 3 years of experience in a regulated environment. Strong communication, project management, and problem-solving skills are essential. The company offers flexible working hours and opportunities for professional development.

Leistungen

Flexible working hours

Professional development opportunities

Competitive compensation

Inclusive culture

Qualifikationen

• 3+ years of relevant professional experience in a regulated environment.
• Hands-on experience in pharmaceutical QC or analytical development.
• Excellent organizational skills and ability to prioritize.

Aufgaben

• Lead end-to-end project for Pharma Analytics.
• Ensure GMP compliance and contribute to audit readiness.
• Coordinate with internal labs, clients, and partners.

Kenntnisse

Project management

Customer orientation

Analytical development

GMP compliance

Problem-solving

Communication

Ausbildung

Degree in life sciences

Tools

LIMS

Office skills

Jobbeschreibung

Job Description

The Eurofins BioPharma Services Network of Companies is a first-class biopharmaceutical outsourcing services partner (Contract Research Organization - CRO), working with pharmaceutical, chemical, biotechnology, medical device, and cosmetic clients.

The network covers the whole chain of drug development thanks to an international network of laboratories and testing units with global reach, uniform QA systems, and high-quality services.

We are looking for a GMP Project Manager Pharma who will contribute to the significant growth of our business by :

Key Responsibilities

• End-to-end project leadership for Pharma Analytics : Analytical Development & Method validation, Dissolution, Chromatography, Particle Testing, Stability Storage, and related subcontracted services within the Eurofins Group
• Project planning and timeline management : define project plans, track milestones, manage POs and risks, and report status to stakeholders
• Technical coordination : review and approve technical documents (plans, protocols, validation reports) and analysis results
• GMP compliance : ensure correct execution of commissioned analytical work per GMP; contribute to audit readiness and continuous improvement
• LIMS configuration : map and configure projects in LIMS and support data integrity best practices
• Stakeholder management : coordinate interfaces between internal labs, clients, and external partners; support new project acquisition
• Quality system contributions : assist in authoring and maintaining SOPs and GMP documentation; support client, GMP, and regulatory audits
• Process optimization : identify and implement improvements to increase efficiency, quality, and throughput at the site

Qualifications

• Degree in life sciences (pharmacy, chemistry, biology) or completed vocational training in a pharmaceutical or chemical field combined with 3+ years of relevant professional experience in a regulated environment ( ISO 17025, GLP, ideally GMP )
• Hands‑on experience in pharmaceutical QC and / or analytical development
• Strong customer orientation with clear, confident communication (written & verbal)
• Very good IT literacy and Office skills; LIMS experience is a plus
• Demonstrated project management capability; certification (e.g., PMP, IPMA) is an advantage
• Excellent organizational skills , prioritization, and problem‑solving in dynamic settings
• High sense of responsibility, reliability, and team spirit
• Language : very good German , good English

What We Offer

• Flexible working hours and the option for partial remote work
• Professional development : training, certifications, and mobility opportunities within the Eurofins Group
• International exposure : projects across the global network with standardized QA systems
• Modern workplace & tools : LIMS-driven environment, digital collaboration, and data integrity focus
• Competitive compensation and attractive social benefits
• Inclusive culture : diversity, equity & inclusion are embedded in our global organization

Additional Information

If we have aroused your interest, we would be delighted if you could send us a personal cover letter, your CV and references.

We look forward to receiving your application!

We support your development! Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.

Weembracediversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer . We prohibit discrimination against employees or applications based on gender identity and / or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.

Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal!

Find out more in our career page : https : / / careers.eurofins.com /

Please note that as per Eurofins policy, we do not accept unsolicited resumes from third‑party recruiters unless such recruiters were engaged to provide candidates for a specified opening. Any employment agency, person or entity that submits an unsolicited resume does so with the understanding that Eurofins will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity.