CDMO Quality Manager – Pharma/GMP (m/f/d)

Your chance with us

Would you like to become part of an internationally operating company in a future-proof industry? Due to our continued growth, we are offering an initial two-year fixed-term position in a modern working environment surrounded by greenery in Dresden, Germany (01328). As a CDMO Quality Manager – Pharma/GMP (m/f/d) , you can expect challenging responsibilities, flexible working-time models, and attractive benefits designed to support a healthy work-life balance.

More than just a job

• An initial two-year fixed-term position in a future-oriented, internationally operating company
• Flexible working-time models to support the compatibility of work and family life
• 30 days of annual leave
• 10 paid days of leave to care for a sick child
• A modern workplace, including height-adjustable desks, in a green and peaceful environment
• Free company parking and electric vehicle charging facilities
• Three additional discretionary sick days
• Access to a wide range of attractive benefits through our ROTOP Benefits Portal
• Company bicycle leasing and a subsidized public transport pass
• Team-building company events that strengthen collaboration and team spirit
• Diverse career and professional development opportunities as well as additional benefits

Your tasks

• Manage CDMO customer projects from a Quality Assurance and pharmaceutical quality perspective
• Support technology transfers, product launches, and GMP-relevant process changes
• Serve as the main contact for external CDMO customers regarding quality-related and regulatory matters
• Review and approve manufacturing, testing, validation, and quality documents in compliance with GMP requirements
• Process and assess deviations, OOS/OOT results, CAPAs, and change controls
• Support batch release activities and prepare and maintain Quality Agreements
• Plan, support, and follow up on customer audits, inspections, and quality-related actions

Your profile

• A successfully completed degree in a natural science, such as pharmacy, chemistry, biology or biotechnology
• Professional experience in pharmaceutical quality assurance, Quality Assurance or a GMP-regulated environment is an advantage
• Knowledge of deviation management, CAPA, change control, OOS/OOT or batch documentation is desirable
• A careful, precise, and GMP-compliant approach to work
• A strong quality mindset and a good understanding of pharmaceutical processes and cross-functional interfaces
• An independent and structured working style, combined with the ability to coordinate complex tasks effectively
• Very good German and English skills for communication with internal departments and international customers

Your team

Become part of a growing team and help us shape the future. Apply now as a CDMO Quality Manager – Pharma/GMP (m/f/d) and take the opportunity to advance your career in a modern and international working environment.

If you would like to contribute your skills in an innovative environment and continue developing both professionally and personally, we look forward to receiving your application.