GMP Project Coordinator - Pharma

Eurofins; Konstanz; On-site; EUR 50,000 - 75,000; Full time

Benefits offered by this job

Flexible working hours

Professional development opportunities

Modern workplace & tools

Competitive compensation

Inclusive culture

Job summary

Stryker Corporation in Konstanz, Germany, is seeking a qualified professional for end-to-end project leadership in Pharma Analytics. The role requires a degree in life sciences or vocational training in a related field along with relevant experience in a regulated environment.

Responsibilities include managing project timelines, ensuring GMP compliance, and coordinating with stakeholders. The position offers flexible working hours and opportunities for professional development within a diverse and inclusive culture.

Qualifications

• 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.
• Excellent organizational skills, prioritization, and problem-solving in dynamic settings.

Responsibilities

• Lead end-to-end project leadership for Pharma Analytics.
• Manage project planning and timelines effectively.
• Ensure compliance with GMP during analytical work.

Skills

Customer orientation

Project management

Organizational skills

IT literacy

Communication (German, English)

Education

Degree in life sciences (pharmacy, chemistry, biology)

Completed vocational training in pharmaceutical/chemical field

Tools

LIMS experience

Job description

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, risks and forecasts, and report status to stakeholders
• Technical coordination: review and evaluate technical customer requests and create appropriate work packages and proposals
• 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 preferably 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
• 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

We embrace diversity! 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.