GMP Specialist – All Gender

This is a fully remote position, open to applicants in Germany.

📋 Description

• You will guarantee compliance with GMP standards in development, production, and/or quality processes.

• You will be responsible for creating, reviewing, and approving SOPs, batch records, deviation reports, as well as CAPA and change-control documentation.

• You will assist in audits, inspections, and qualifications.

• You will execute process validations (CQV, CSV) and provide training within a GxP environment.

• You will engage in interdisciplinary projects aimed at process optimization, data integrity, and digitization.

• You will collaborate closely with Production, Quality Control, Regulatory Affairs, and Engineering teams.

⛳️ Requirements

• A degree in Pharmacy or a related scientific field.

• A minimum of three years of professional experience in a regulated environment (GxP, ISO 13485, MDR, etc.).

• Familiarity with quality assurance, validation, documentation, or production processes.

• A team-oriented attitude, driven by goals, and highly dedicated.

• Proficiency in both German and English, written and spoken.

🏝️ Benefits

• Talent Management – we invest in your career development.

• Work–life balance – enjoy flexible working hours and the option to work remotely.

• Fit and relaxed – access to EGYM Wellpass.

• Enjoy biking – take advantage of company bike leasing.

• Green Mobility – enjoy discounted travel options.

• We also provide a permanent contract, corporate benefits, and team events.