Quality Assurance Manager (all genders) Product Life Cycle Management

Midas Pharma GmbH.; Frei-Weinheim; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A well-established pharmaceutical company in Germany seeks a dedicated professional to supervise development projects for finished medicinal products. Ideal candidates will have several years of experience in the pharmaceutical industry, strong knowledge of GxP guidelines, and expertise in validation. The company offers a secure, respectful working atmosphere, flexible working hours, and various benefits including comprehensive training opportunities.

Leistungen

Flexible working hours

30 days' vacation

Comprehensive training opportunities

Employee restaurant

Regular events

Qualifikationen

• Several years of professional experience in the pharmaceutical industry, particularly in manufacturing finished medicinal products.
• Very good knowledge of GxP guidelines and relevant ICH guidelines.
• Expertise in validation according to EU GMP Annex 11 and Annex 15.

Aufgaben

• Supervision of development projects for finished medicinal products up to market launch.
• Processing of complaints, deviations and change requests.
• Creation, review and maintenance of quality documents.

Kenntnisse

Strong communication

Teamwork

Responsibility

Decision-making

Very good knowledge of German

Very good knowledge of English

Ausbildung

Successfully completed scientific or technical studies

Jobbeschreibung

Your mission

• Supervision of development projects in interdisciplinary teams for finished medicinal products up to market launch and throughout the entire product life cycle.
• Processing of complaints, deviations and change requests
• Creation, review and maintenance of quality documents (e.g. MBR, PQR, risk assessments, stability program)
• Coordination of all quality-relevant topics relating to finished products with the quality units of our manufacturing partners and our customers
• Presentation of quality processes in customer audits, inspections by authorities and internal audits
• Support in the planning, coordination, and implementation of the validation of computer-based systems in accordance with applicable regulations

Your profile

• Successfully completed scientific or technical studies
• Several years of professional experience in the pharmaceutical industry, particularly in the area of manufacturing finished medicinal products
• Very good knowledge of GxP guidelines and the relevant ICH guidelines
• Expertise in validation according to EU GMP Annex 11 and Annex 15
• Strong communication and teamwork skills
• Enjoy taking responsibility and making decisions
• Very good knowledge of German and English

Our Offer

• We are looking for you as a personality and want you to make an authentic contribution - we encourage this in turn by giving you plenty of scope for creativity and independence
• A career in sales combined with interesting and challenging tasks in a dynamic, constantly growing company
• A secure job in an established and renowned family business that offers you the security of over 35 years in business as well as a personal and respectful working atmosphere
• We have flat hierarchies and small teams - this enables us to have clear and direct communication channels that lead to quick decision-making processes
• Flexible working hours and 30 days' vacation
• Comprehensive training opportunities with a fixed annual training budget
• Various benefits such as JobRad, EGYM Wellpass, employee restaurant, regular events and much more.