Main tasks
Management and coordination of the QC New Product Introduction (NPI) department of quality control for the launch of new pharmaceutical products
Responsible for compliance with quality standards and project timelines
Creation and review of cGMP documents (method transfer, validation protocols, reports, work instructions, device qualification documentation)
Supervision of the implementation of training and analyses for the introduction of new test methods
Processing deviations and implementing corrective measures
Coordination and supervision of problem-solving activities
Collaboration in international analytical projects (organization/participation in international telephone conferences)
Participation in audits and inspections in connection with the introduction of new products into quality control
Your profile
For this interesting and varied position, we are looking for a team player, communicative and proactive personality with a high degree of quality awareness, resilience and flexibility. You are characterized by an independent, precise and goal-oriented way of working as well as reliability and adherence to deadlines. You also have the following professional qualifications:
Degree in biochemistry, chemistry or comparable training
Professional experience in a GMP-regulated environment
Experience in leading diverse teams
Experience in working in an international matrix environment (especially in negotiating activities with multiple stakeholders)
Experience in method transfer/validation preferred
Project management experience
Fluent in written and spoken English and German
Confident handling of MS Office
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