Senior Manager Quality (m/f/d)

About Us:

The Hamburg-based EVP Group connects and coordinates the competencies & resources of medium-sized Consumer Health Care (CHC) companies with differentiated regional and indicative focuses. The core market of our rapidly growing group is Europe, but we also distribute our products worldwide.

We support customers from trade and industry in the development of their own CHC brands with continuously new, trend-oriented product developments. Our full service covers the entire spectrum of services, from tailor-made ideas to the shelf. With our own, individually positioned brands, we also offer attractive solutions for personal health management to differentiated consumer target groups.

Within the group, we currently supply over 500 articles across all regulatory categories (over-the-counter medicinal products, medical devices, dietary supplements, and cosmetics), covering common indications from colds to beauty, as well as all dosage forms from solid to liquid. We rely on high quality standards and innovative technologies and ingredients.

The Team:

To support our team at the Leipzig or Hamburg location, we are looking for a new colleague (m/f/d) in full-time (40h/week).

These tasks await you:

• Technical leadership of a team to ensure GMP and regulatory compliant manufacturing, testing, and release of medicinal products according to AMG and AMWHV, together with external qualified persons.
• Technical leadership of and participation in projects in the field of medicinal products, especially transfers of manufacturing operations.
• Evaluation of PQRs including ongoing stability studies.
• Processing and negotiation of scope of responsibilities agreements with suppliers and customers.
• Communication with EVP's B2B customers on topics related to the quality of medicinal products.
• Evaluation and assessment of complaints regarding the quality of medicinal products (interface to external QPPV).
• Evaluation and assessment of deviations and ensuring an efficient change control system.
• Participation in and execution of GMP audits, production support, and self-inspections, as well as supplier, authority, and customer audits (interface to QM).
• Coordination and participation in the creation of SOPs for the description of process flows.
• Planning and follow-up of the medicinal product budget, creation or participation in relevant business cases, price negotiations with Q service providers.
• Participation in regular further and continuing education.

We are looking for you!

• Successfully completed scientific degree, e.g., in Pharmacy, Chemistry, or Biology; PhD is an advantage.
• Good knowledge and comprehensive practical experience in implementing legal requirements for the quality of medicinal products, e.g., in collaboration with qualified persons.
• Practical experience in pharmaceutical production and/or quality control is advantageous.
• Analytical, process- and solution-oriented thinking and acting.
• High motivation, hands-on mentality, willingness to shape, and goal orientation.
• Independent, systematic, and structured way of working.
• Very good organizational skills.
• Experience in project management.
• Good team and communication skills, stakeholder management, and assertiveness.
• Willingness to travel.
• Negotiation-level German and English skills in speaking and writing.
• Confident use of all standard MS Office applications (e.g., Word/Excel/PowerPoint/Outlook/Sharepoint).

We offer you!

a workplace in a company with high innovative strength, operating in a constantly growing and exciting market.
Look forward to a qualified, motivated, and collegial team in an environment with flat hierarchies and short decision-making paths. We are constantly at the forefront and wish for colleagues (m/f/d) who actively contribute their ideas, think holistically across departments, and want to drive things forward together as a team.

Your contact person

If you would like to get to know us, we look forward to receiving your application with your earliest possible start date.

Questions about the position can be answered in advance by Christopher Oehmig,

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