Quality Specialist Systems
- Location
- United States
- Listed
- 3 days ago
About the role
- Degree in pharmacy, human/veterinary medicine or natural sciences or similar
- At least 2 years' experience as a Quality Manager in the pharmaceutical industry, ideally in a sales and marketing-oriented company
- Sound knowledge and experience in pharmaceutical manufacturing, development or testing
- Strong knowledge of EU and German legal and regulatory requirements (GMP/GDP, AMG, AMWHV, BtMG, MPG)
- Knowledge of drug approval
- Very good user skills in Excel, Access and PowerPoint
- Business fluent in German and English
From Zentiva's careers page, first listed on Rolev.ai on November 6, 2026. Rolev.ai is not the employer.
How Rolev.ai helps with this application
Rolev.ai is a job search and application tool for US job seekers. For this Quality Specialist Systems role at Zentiva, it shows how your resume fits, tailors your resume to the posting, and prepares the application for you to review.
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Common questions
Where is the Quality Specialist Systems job at Zentiva located?
This Quality Specialist Systems position at Zentiva is located in United States. Always check Zentiva's application page for specific state eligibility or relocation policies.
How do I apply for the Quality Specialist Systems position at Zentiva?
This listing links directly to Zentiva's Workday application page. You can apply directly on Zentiva's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.