QC Expert
at wega Informatik
Visp, VS, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 01 Jan, 2025 | Not Specified | 06 Oct, 2024 | N/A | Product Manufacturing,Biology,Testing,It,Chemistry,Interdisciplinary Collaboration,Microbiology | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
On behalf of our customer in the life sciences field, we are seeking a 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 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
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
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Pharmacy chemistry or biology or an equivalent education
Proficient
1
Visp, VS, Switzerland