Responsibilities: Assurance of GMP compliance of all manufacturing and QC testing activities at the site. Assurance of qualification of raw material suppliers. Leading of the site Quality team. Member of the site leadership team and global business unit quality team. Leading of global quality teams for specific global quality projects. Planning and supervision of the quality budget of the site. Support of the site continuous improvement process (lean six sigma). Interaction with customers for quality related projects and product development activities. Finished product release according to §19 AMG. Development of quality plan and strategies. Implementation and review of quality KPIs. Leading the quality management review system. Leading of regulatory GMP inspections of the site. Assuarance of compliance in food and medical device regulations.

Responsibilities: Assurance of GMP compliance of all manufacturing and QC testing activities at the site. Assurance of qualification of raw material suppliers. Leading of the site QPD team and development of team members. Member of the site leadership team and global business unit quality team. Leading of global quality teams for specific global quality projects. Planning and supervision of the quality budget of the site. Support of the site continuous improvement process (lean six sigma). Interaction with customers for quality related projects and product development activities. Finished product release according to §19 AMG. Leading of the New Product Implementation team. Development of quality plan and strategies. Implementation and review of quality KPIs. Leading the quality management review system. Leading of regulatory GMP inspections of the site. Budget responsibility for Quality and Product Development Teams.

Responsibilities: Assurance of GMP compliance of all manufacturing and QC testing activities at the site and at contract manufacturers. Leading of the site quality team and development of team members. Member of the site leadership team and global business unit quality team. Planning and supervision of the quality budget of the site. Support of the site continuous improvement process (lean six sigma). Development of innovative quality strategies such as PAT and real time release. Representing Pfizer in Pharmaceutical Drug Manufacturer Association (VfA Unterausschuss)

Responsibilities: Assurance of compliance of manufacturing and testing processes with the registration dossier. Review and approval of changes according to Pfizer quality policy. Review and approval of product quality reviews and identification of process improvement projects. Review and approval of quality agreements with contract manufacturers. Support of registration departments for regulatory requests.Additionally as QP function: Review of manufacturing and testing records and final release of finished products to the market (QP release).

Responsibilities: Assurance that raw materials and finished products (patient packs) used for clinical supplies are tested according to specifications, randomisation plan and GMP requirements. Leading of QC testing team and supervision of operators. Planning of resources. Technical support of dosage form development projects. Review of maunufacturing records and final release of patient packs according to AMG.

Responsibilities: Assurance that raw materials and finished products are tested according to registered specification and GMP requirements. Leading of QC testing team and supervision of operators. Planning of resources. Scheduling of QC testing according to production plan.