QA for QC Expert
wega Informatik AG
Publication date:
02 October 2024Workload:
100%Contract type:
Permanent position- Place of work:Visp
On behalf of our customer in the life sciences field, we are seeking a QA for QC Expert who will play a fundamental role in ensuring highest quality standards of their products.
Start date: asap
Duration: 1 year (extension possible)
Workload: 80 - 100%
Location: Visp (3 days onsite)
Your Area of Responsibilities:
- Supporting the QC department in the GMP-compliant set-up of QC laboratories and their processes. Furthermore, create all required documents to define QA for QC processes.
- Being responsible for the timely release of documents (e.g. SOPs, qualification documents, specifications, test methods and method validations) related to Drug Product testing
- Quality oversight of QC- and that QC processes comply with applicable legal and regulatory requirements
- Ensure a high level of quality in accordance with GMP guidelines
- Support the entire QC team in various topics and contribute ideas for the ongoing optimization and further development of procedures, working methods and processes
Your Qualification and Experience:
- University degree in pharmacy, chemistry or biology or an equivalent education
- Proven track record in a QA area in a GMP-regulated environment for drug product manufacturing or testing
- Experience in microbiology and QC is an advantage
- Fluent in German and English (writing and speaking)
- Works independently, efficiently, are a team player and appreciate interdisciplinary collaboration
- Proactive, thinks outside the box and a willingness to take on responsibilities
- Demonstrates a high degree of flexibility when it comes to solving problem