Our company is further expanding by setting up a brand-new manufacturing site located in Nidau. Due to our company’s continued growth and expansion, we are recruiting a professional for the position of
Job Description
In this position, you will work across multiple tasks within our growing Quality Team.
1. Responsible for various laboratory testing for materials and products (LAL, sterility testing).
2. Collect water samples for testing (TOC, HPC, Conductivity) to be sent to external suppliers.
3. Compile and document data from test procedures to ensure accurate records and compliance with quality and regulatory standards.
4. Manage laboratory consumables, including inventory monitoring, organization, and timely ordering to ensure uninterrupted lab operations.
5. Lead and/or assist in project planning, coordination, and tracking by supporting timeline development, maintaining project documentation, and facilitating communication between team members.
6. Support the preparation of investigations, summaries, and reports by reviewing data for compliance with specifications and reporting deviations or abnormalities.
7. Provide technical support to the QC Manager in troubleshooting, method development, and process improvements.
8. Maintain and update Standard Operating Procedures (SOPs) and Work Instructions (WIs) relevant to your functional area, ensuring documentation is accurate, current, and aligned with regulatory and operational requirements.
9. Support internal and external audits by preparing documentation, responding to auditor queries, and implementing corrective actions as needed.
10. Foster strong collaboration with cross-functional teams (e.g., Quality Assurance, Manufacturing, Purchasing) to support shared goals and continuous improvement.
11. Perform additional responsibilities as required to support the Quality Control function and adapt to evolving business needs.
Your Profile
1. Degree in Microbiology, Biology, or a related scientific field preferred.
2. Experience in a GMP-regulated laboratory environment, preferably within the medical device or pharmaceutical industry.
3. Experience in an FDA- and ISO 13485-regulated environment.
4. Minimum of 3 years’ relevant experience preferred.
5. Excellent English skills, both spoken and written; additional languages are an asset.
6. Proficient IT skills (e.g., MS Office, eQMS, etc.).
7. Highly flexible and adaptable to change, with the ability to work under pressure.
8. Responsible, team-oriented, well-organized, with a strong attention to detail.
The Right Decision: Working at STAAR Surgical
STAAR Surgical offers an ideal environment to develop your career and progress professionally and personally within a multicultural and international company. Our benefits include:
* 40 working hours per week
* Modern working spaces
* Minimum of 25 days of vacation
* Modern cafeteria spaces
* Monthly contribution to health insurance costs
* Training and development plans
* Free parking spaces and excellent connections to public transportation
* Regular social events, such as summer and winter parties
If you want to contribute to the evolution in visual freedom and become part of our passionate team, please send your full application via email.
For more information, contact our HR Team at (032 33288 88) or visit us online at www.staar.com.
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