Senior Analyst handling HR Operations and candidate onboarding in Noida, India. Ensuring efficient processes and supporting client expectations through effective communication.
About the role
- Consultant GMP-Compliance & Qualitätssicherung für die Unterstützung renommierter Pharmaunternehmen. Durchführung von Qualifizierungen und Validierungen in der pharmazeutischen Industrie.
Responsibilities
- Contribute to the development of optimized qualification and validation concepts
- Execute qualifications of high‑tech equipment/systems in the pharmaceutical and biopharmaceutical industry
- Participate in risk analyses
- Support validation projects (e.g., cleaning, process and method validations)
- Prepare GMP‑compliant documentation, including Standard Operating Procedures (SOPs)
- Review technical documents and drawings, as well as changes and deviations
Requirements
- Degree in Process Engineering, Pharmaceutical Engineering, Biotechnology, Chemical Engineering, Life Sciences Engineering, or a comparable engineering or natural sciences program
- Strong technical understanding and the ability to quickly familiarize yourself with different areas of responsibility
- Experience in a GMP environment is an advantage
- Independent and solution‑oriented working style
- Willingness to travel for on‑site qualification activities; Class B driving license required
- Excellent German and good English skills
Benefits
- Exciting and varied projects
- A collegial team and a supportive mentor
- Flexible location and working hours model, plus permanent employment contracts
- Internal and external training and development opportunities
- Open corporate culture with short decision‑making paths
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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