Quality Manager (m/f/x) – Heidenheim a. d. Brenz/Berlin/remote

The Force CT GmbH; Giengen; Hybrid; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading company in the healthcare sector seeks a Quality Manager to ensure compliance with GMP standards. You will leverage your extensive experience in quality assurance to support various projects. The role offers flexibility in work arrangements and emphasizes a solution-oriented and proactive mindset.

Qualifikationen

• Several years of experience in quality assurance in manufacturing.
• Familiarity with GMP quality systems.
• Fluency in German and English.

Aufgaben

• Ensuring quality control and production compliance.
• Hands-on experience with essential pharmaceutical processes.
• Proactive communication and independent work.

Kenntnisse

Quality assurance

GMP quality systems

Process validation

Communication

Jobbeschreibung

General Information

Position: Quality Manager (m/f/x)

Location: one of our offices in Heidenheim a.d.Brenz/Berlin or remote (Germany)

Starting: at the next possible date

Who We Are

THE FORCE builds companies on behalf of clients in the healthcare, pharmaceutical, and medical device sectors, supporting or managing customer projects of various kinds, and providing qualified personnel to address bottlenecks or problems.

We promote a flexible working environment and embrace diversity in gender, nationality, religion, and working styles. Our unique culture aims to seamlessly integrate employees and partners into one organization.

Our organization is adaptable to customer structures, enabling us to solve problems swiftly, effectively, and efficiently.

People Are Our Strength

People are our most valuable asset and the core of our success. We prioritize flexibility in working hours, location, and tasks, and value your individual talents. We seek that certain something in our team members and are committed to nurturing it.

What Will Allow You To Dive In Right Away

• Several years of experience in quality assurance within a manufacturing pharmaceutical company, ideally with close links to production and/or quality control.
• Familiarity with GMP quality systems and practical experience in various processes.
• Good understanding of German and European laws and standards related to GMP/GDP.
• Hands-on experience with process validation, equipment and premises qualification, and technology transfer.
• Fluency in written and spoken German and English for effective communication.

What Will Be The Wind Beneath Our Wings

• A solution-oriented mindset.
• Efficiency in work without compromising precision.
• Ability to work independently and seek help when needed.
• Proactive and concise communication style.
• High quality awareness, reflection, continuous learning, and skill improvement.

What Will Make You Fit The Bill Even More

• Additional practical experience or specialization, e.g., electronic systems introduction.
• Experience in manufacturing processes of various pharmaceuticals such as non-sterile, solid and liquid dosage forms, parenterals, biologics, or radiopharmaceuticals.
• Successful project management experience.
• Commercial mindset and ability to develop new business ideas or projects.

SOUNDS LIKE YOUR NEW NEST?

Find out if we can flock together and send your application to Tanja Reischl-Stenske.

Please include your CV, cover letter, and any additional documents in English or German.