Employee (m/f/d) Quality Assurance

Eckert & Ziegler Strahlen- und Medizintechnik AG; Braunschweig; Vor Ort; EUR 50.000 - 65.000; Vollzeit

Zusammenfassung

A leading radiopharmaceutical company in Braunschweig is seeking a Quality Management professional to support and develop their QM system in compliance with EU GMP guidelines. Key responsibilities include implementing QM processes, documentation, and conducting audits. Ideal candidates should have a scientific background, initial experience, and be fluent in German and English. This role offers stability, competitive salary, and a family-friendly environment with flexible working hours and numerous benefits.

Leistungen

Flexible working hours

30 days holiday

Health insurance

Company pension scheme

Bicycle leasing offer

Qualifikationen

• Initial professional experience in the field of Quality Management.
• Independent, structured and efficient way of working.

Aufgaben

• Support in maintenance of the QM system for pharmaceuticals.
• Implementation and support of QM processes.
• Monitoring QM processes implementation.
• Documentation tasks like writing QA instructions.
• Conducting internal audits and supplier audits.
• Planning and conducting employee training.

Kenntnisse

Knowledge of GMP

Proficient in MS Office programs

Fluent in German

Fluent in English

Strong communication skills

Teamwork ability

Ausbildung

Successfully completed scientific studies

Jobbeschreibung

CONTRIBUTING TO SAVING LIVES | WIR HELFEN ZU HEILEN

Eckert & Ziegler Radiopharma GmbH, a subsidiary of the renowned and internationally active Eckert & Ziegler Group, has been an important and reliable partner to the radiopharmaceutical industry for over 20 years.

Radiopharmaceuticals have become an indispensable part of modern medicine. They play a particularly important role in the research and development of new therapeutic options, but also in the treatment and diagnosis of various types of cancer. We supply clinics, pharmaceutical companies and institutes with GMP-compliant radioisotopes and radiopharmaceuticals and develop tailor‑made solutions for research companies. With our support, new processes and methods are created from development to production.

Join our ambitious and highly skilled team and help to heal.

Your contribution to success

• Support in the maintenance and further development of the QM system for the production of pharmaceuticals and medical devices at the Braunschweig site in accordance with the EU GMP guidelines, ISO 9001 and ISO 13485
• Implementation and support of QM processes (deviation, CAPA, change control, complaint, internal audits, etc.)
• Monitoring the implementation of QM processes
• Documentation tasks (e.g. writing QA instructions / SOPs)
• Support in conducting internal and supplier audits
• Planning and conducting employee training

This qualifies you

• Successfully completed scientific studies
• Initial professional experience in the above-mentioned field of activity
• Knowledge of GMP, ISO 9001 and ISO 13485 desirable
• Proficient in using MS Office programs
• Fluent written and spoken German and English
• Independent, structured and efficient way of working
• Strong communication skills and ability to work in a team

You can look forward to

• Family‑friendly organisation with flexible working hours, no weekend or shift work
• Stable and secure job
• Attractive salaries and benefits, as well as a company pension scheme
• 30 days holiday and paid time off for special reasons, such as relocation, wedding or sick child days
• Health benefits, such as health insurance and health days
• Interesting and challenging work with a high degree of personal responsibility
• Bicycle leasing offer
• Pleasant working environment in a dedicated team
• Opportunities for individual development
• Flat hierarchies and short decision paths
• Catering options in the company canteen
• Parking and good public transport links

We look forward to receiving your application!

Please apply by using our online application form, which can be easily access by clicking on the "Apply Now" button at the end of each vacancy.

In our search for new talent, we welcome all applications regardless of gender, age, race, sexual identity, disability, religion or belief. We value diversity and the different perspectives you can bring to our business. We welcome your application even if you do not meet all of the criteria, because we value individual skills, motivation and potential over categorisation.

Show us what makes you special. Take the next step in your career and send us your informative application documents, stating your salary expectations and your earliest possible starting date.

Do you have any questions? Please contact us: