Head of Quality Assurance - CDMO (m/f/d)

Head of Quality Assurance – CDMO (m/f/d)

On behalf of our client, a globally successful company specializing in the development and production of aseptically produced pharmaceuticals, we are seeking a Head of Quality Assurance (m/f/d). Our client offers comprehensive services and is the competent partner for the entire value chain up to market introduction and commercial production. For over 25 years, they have demonstrated continuous growth, thanks to the dedicated efforts of their employees at the most modern production facilities.

Main Responsibilities:

• Management of the Quality Assurance department, including the sub-areas of Quality Systems and GMP Compliance, and associated staff positions.
• Taking responsibility for a reliable and effective quality assurance system, including the areas of Deviation, CAPA, Change Control, Complaint Management, Training, Batch Record Review, and its continuous development in line with international regulations.
• Responsibility for local administration and participation in the further development of the electronic document management and quality management system within the company group.
• Ensuring the implementation of new regulatory requirements.
• Conducting customer audits and regulatory inspections on-site.
• Preparation and implementation of management reviews.
• Provision of relevant quality-descriptive KPIs.
• Supporting the department head in strategic management and planning within the department.

Key Requirements:

• Completed scientific Master\’s or FH degree, such as Biotechnology or Pharmaceutical Technology.
• Extensive practical experience in the field of quality assurance in the pharmaceutical industry.
• Experience in leading employees.
• Very good knowledge and experience in the application of national and international laws and regulations (e.g., EU GMP Guide, Aseptic Guide, etc.).
• Very good English skills, both spoken and written.

What\’s in it for you?

• A broad, interesting, and responsible range of tasks awaits you.
• The opportunity to implement projects independently.
• Demand-oriented IT training and further education.
• You will start in a permanent employment relationship.
• A dynamic and motivated team looks forward to welcoming you.
• Attractive conditions, a wide range of offers for work-life balance, and an excellent training offer.

Seniority level: Director

Employment type: Full-time

Job function: Quality Assurance

Industries: Pharmaceutical Manufacturing

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