Associate scientist Jobs in Nidderau
- Gesponsert
Natural Scientist as Qualified Person / QP (f / m / d)
STADA Arzneimittel AGBad Vilbel, DE
Scientist (m / w / d) Analytik & Downstream Processing in Frankfurt
GELITA AGHessen, DE
Sr. Clinical Research Associate
AvaniaHesse, DE
Distribution Sales Manager - DACH Region
Hypertherm AssociatesHanau, Germany- Gesponsert
Analytics Engineer (w / m / d) - Business Analysis, Ingenieur
LotumBad Nauheim, DE
Data Scientist / Data Analyst / Data Engineer (m / w / d) bis zu 7.000€
Tech Staff Solutions Heidelberg GmbHHanau, Hessen, DE
Fachinformatiker für Systemintegration (m / w / d)
Herrmann Personaldienste GmbHHanau, Hessen, DE
Director RWD Scientist
SEC Life SciencesHessen
Associate Finance 1+
Schollmeyer&SteidlHessenNatural Scientist as Qualified Person / QP (f / m / d)
STADA Arzneimittel AGBad Vilbel, DE- Vollzeit
Caring for People's Health as a Trusted Partner" - This mission motivates us at STADA every day to improve the health of people worldwide. With our wide range of generics, consumer health products and specialty pharmaceuticals, we offer patients, doctors and pharmacists a wide range of therapeutic options.
Around 11,700 employees live our values of Integrity, Entrepreneurship, Agility and One STADA. Together we are on an exciting growth journey and want to successfully shape the future of STADA.
Do you want to become part of a dynamic, international team and grow with us? Then apply now as :
Qualified Person / QP (f / m / d)
Bad Vilbel | Germany (DE) | Full-time | Permanent | Quality | Management / Executives
What you can expect
As a Qualified Person (m / f / d) in Finished Product Control, you take on the critical responsibility as a Qualified Person according to §14 AMG and as the Head of Quality Control according to §14 AMWHV for products not manufactured and packaged at the Bad Vilbel site.
- You ensure that each batch is manufactured and tested in accordance with legal regulations
- You approve or reject bulk and finished products and sign the corresponding test protocols
- You approve specifications, sampling instructions, and testing instructions and ensure compliance with them
- You determine the required scope of testing and monitor implementation, considering legal frameworks, GMP guidelines, and cost-effectiveness
- You address issues arising from daily operations
- You ensure the implementation of QS-relevant parts of CCPs / MOCs
- You handle deviations and test reports as well as OOS-specific issues
- You organize departmental documentation in accordance with GMP guidelines
- You evaluate PQRs (Product Quality Reviews) and stability studies
Who we are looking for
What we offer
We look forward to receiving your application via our . At jobs.stada.com you will also find numerous other job opportunities, as we are always looking for motivated talents who can strengthen our team with their expertise and personality. Do you have further questions? Then please reach out to . We will consider requests to work part-time on an individual basis. Please contact us in advance by e-mail ([email protected]) and let us know how many hours per week you would like to work.
STADA Group promotes its diverse culture, regardless of gender, age, social or ethnic origin, disabilities, religion, ideology or sexual orientation. We use the strength of this diversity to develop creative ideas, expand our experience and increase innovative strength. Our focus is on equal opportunities, respectful cooperation and the promotion of an inclusive working environment. #LI-DH1