Team Leader Quality Assurance (m / f / d)

We create lasting connections : Thanks to our trustworthy contacts with local HR decision-makers, we can offer you attractive jobs with successful companies in the pharmaceutical industry in Frankfurt am Main. We are currently looking for a Supervisor in Quality Control. Are you a pharmacist or biotechnologist looking for a secure job with fair pay and long-term prospects as a QC Lab Team Supervisor? You will find what you are looking for with us - apply now! Our working atmosphere and the openness of our teams promote equal opportunities for all people - including those with disabilities, whose applications we welcome.

Here’s what we offer

• Above-average salary
• Attractive social benefits, for example vacation and Christmas bonuses
• Vacation entitlement of up to 30 days per year
• Opportunity to be taken on by our business partner
• Regular team events such as summer parties and Christmas parties
• Monthly changing employee offers, e.g. for technology, fashion, cars, etc.

Your tasks

• Ensuring the timely execution and documentation of quality inspections of pharmaceutical products in compliance with GMP guidelines and other requirements
• Implementation and support of required quality assurance systems, e.g. failure investigation, under the responsibility of the responsible quality management and head of quality control
• Implementation of the inspection-compliant quality concept by contributing expert knowledge during inspections by the authorities and internal quality audits
• Implementing regulations on occupational safety and health and environmental protection (HSE) and monitoring compliance with these rules
• Maintaining and approving sampling plans, test methods and test specifications as well as the associated acceptance criteria
• Planning, coordination and evaluation of verification, validation and transfer studies in compliance with relevant internal and external guidelines
• Implementing data integrity specifications and ensuring compliance
• Preparation of the annual product evaluation
• Processing complaints in relation to laboratory tests
• Collaboration in project teams

Your profile

• Successfully completed scientific studies
• Professional experience desirable
• Ideally initial experience in managing employees
• Knowledge of GMP and expertise in QC
• Experienced with MS Office
• Good written and spoken English skills
• Independent, proactive and conscientious way of working as well as quick comprehension skills
• Willingness to perform and a strong sense of responsibility

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