Munich: Quality Manager Supplier Qualification (m/f/d)

TRIGA – Wir vermitteln nicht nur Personal, sondern Menschen. Engagiert, erfahren und erfolgreich. Mit umfassender und individueller Karriereberatung, branchenspezifischem Know-how und einem weitreichenden Netzwerk bieten wir eine Vielfalt attraktiver Vakanzen.

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.

Your Responsibilities:

• 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

Your Profile:

• 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 English skills
• Oracle knowledge is desirable

What the company offers:

• 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

Contact:

Mariana Chaumont
Senior Consultant
089-809130720
chaumont@triga-consulting.de