Director Quality Control

4w4 weeks ago

Ferring Pharmaceuticals

DE · Full-time · €110,000 – €140,000

About this role

Ferring GmbH is the German production arm of a rapidly expanding international pharmaceutical group headquartered in Saint-Prex, Switzerland. In Kiel, we manufacture critical products for reproductive medicine, endocrinology, urology, pediatrics, and gastroenterology, specializing in sterile dosage forms and peptide hormones.

As Director Quality Control, you will hold overall responsibility for quality control of raw materials, intermediates, and bulk products, as well as stability management. You will lead the Analytics & Pharmacology, Microbiology & Pharmacology, Validation & Services, and Stability teams, driving the strategic development of the QC organization.

Reporting directly to the Managing Director of Ferring GmbH, you will be a member of the local management team. Your day-to-day work involves ensuring compliance with §14 AMWHV, overseeing pharmaceutical quality testing, managing budgets and investments, and coordinating with regulatory authorities including local agencies and the FDA during audits and inspections.

This role offers the opportunity to shape the future of a key production site within a global company that values research and development. With about 500 employees in Kiel and subsidiaries in nearly 60 countries, you will have a tangible impact on products that reach patients in 110 countries worldwide.

Requirements

Completed degree in Chemistry, Pharmacy, or a comparable natural science field
At least 10 years of experience in pharmaceutical quality control
In-depth knowledge of GMP and regulatory requirements, including §14 AMWHV
Proven leadership experience in managing multiple teams and driving strategic development
Experience with international regulatory inspections, such as from FDA or local authorities
Strong understanding of analytical methods, microbiology, and stability management
Ability to manage budgets, investments, and service contracts effectively

Responsibilities

Assume overall responsibility for quality control according to §14 AMWHV
Organize and conduct pharmaceutical quality testing of raw materials, intermediates, and bulk products
Lead, develop, and strategically align multiple QC teams, including Analytics & Pharmacology, Microbiology & Pharmacology, Validation & Services, and the Stability team
Implement and advance the occupational safety management system
Manage budget planning, budget control, and investment decisions for the QC department
Create and continuously improve specifications and test methods in close collaboration with the Qualified Person
Adapt test methods to the current state of science and technology
Serve as an active contact for national and international authorities (e.g., local agencies, FDA) and accompany audits at contract laboratories, contract manufacturers, and internal self-inspections