Our client is an internationally operating pharmaceutical company specializing in the biotechnological production of active ingredients.
Located in Munich, the company offers an exciting opportunity to take on a role in a dynamic and innovative environment.

Aufgaben

• Responsible for the qualification and requalification of existing and potential suppliers in collaboration with local interfaces and the global supplier qualification team, considering documentation and supplier history
• Preparation, planning, and participation in supplier audits as well as their documentation
• Development, distribution, and evaluation of supplier questionnaires
• Tracking and assessing corrective actions from supplier audits
• Supporting other global sites in conducting relevant supplier audits
• Coordinating and supporting audit activities when outsourcing to qualification service providers
• Assessing internal change requests (Change Control process) and requests from contract manufacturers, as well as monitoring internal processes and measures
• Drafting, negotiating, and making technical decisions regarding the content of quality-related responsibility agreements in coordination with department management, qualified persons, and relevant specialist departments, in accordance with local and global requirements
• Preparing key performance indicators (KPIs) for the supplier qualification and responsibility agreement area
• Supporting internal audits, customer audits, and regulatory inspections within the assigned area of responsibility
• Managing and maintaining manufacturer and supplier information as well as archiving supplier documentation
• Drafting and reviewing SOPs and signing them off for the Quality Affairs department
• Contributing to the quality assurance system and compiling data for the Quality Management Review (QMR)
• Supporting the team in the release of finished pharmaceutical product batches
• Taking on special assignments as directed by superiors

Qualifikation

• Completed studies in pharmacy, life sciences, or a completed PTA (pharmaceutical technical assistant) training
• Professional experience in the pharmaceutical industry in quality assurance, quality control, or manufacturing is desirable
• High sense of responsibility and reliability
• Good MS Office skills
• Very precise and structured working style
• Strong communication skills and conflict management ability
• Excellent German and English skills
• Oracle knowledge is desirable

Benefits

• 2 days Homeoffice
• Performance-based bonus
• Employee discounts via Corporate Benefits
• Work-life benefits such as flexible working hours and the possibility of home office
• 30 days of vacation plus additional bridge days off
• Subsidy for the Germany Ticket and excellent accessibility by public transport
• Company pension scheme
• Disability insurance

Please refer the Job description for details