Quality Control Analyst 100%
Infos sur l'emploi
- Date de publication :08 mai 2025
- Taux d'activité :100%
- Type de contrat :Durée indéterminée
- Langue :anglais (Courant)
- Lieu de travail :Hauptstrasse 104, 2560 Nidau
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 as
Job Description
In this position, you will work across multiple tasks within our growing Quality Team.
- Responsible for various laboratory testing for materials and product (LAL, sterility testing)
- Collect water samples for testing (TOC, HPC, Conductivity) to be send to external supplier
- Compiles and documents data from test procedures to ensure accurate records and compliance with quality and regulatory standards.
- Responsible for managing laboratory consumables, including inventory monitoring, organization, and timely ordering to ensure uninterrupted lab operations.
- Lead and/or assist in project planning, coordination, and tracking by supporting timeline development, maintaining project documentation, and facilitating communication between team members.
- Supports the preparation of investigations, summaries, and reports by reviewing data for compliance with specifications and reporting any deviations or abnormalities.
- Provide technical support to the QC Manager in troubleshooting, method development, and process improvements.
- Responsible for maintaining and updating Standard Operating Procedures (SOPs) and Work Instructions (Wis) relevant to their functional area, ensuring documentation is accurate, current, and aligned with regulatory and operational requirements.
- Support internal and external audits by preparing documentation, responding to auditor queries, and implementing corrective actions as required.
- Foster strong collaboration with cross-functional teams (e.g., Quality Assurance, Manufacturing, Purchasing) to support shared goals and continuous improvement.
- Carries out additional responsibilities as required to support the Quality Control function and adapt to evolving business needs.
Your profile
- Degree in Microbiology, Biology or related scientific field preferred
- Experience in a GMP-regulated laboratory environment, preferably within the medical device or pharmaceutical industry.
- Experience in an FDA- and ISO 13485-regulated
- Minimum 3 years’ experience of relevant experience preferred
- Excellent English skills, both spoken and written. All other languages are an asset
- Proficient IT Skills (e.g. MS Office, eQMS, etc.)
- Very flexible and adaptable to change with ability to work under pressure
- Responsible, team oriented and well-organized personality with a strong attention to details
The right decision: working at STAAR Surgical
STAAR Surgical offers you the ideal environment to develop your career and to progress professionally and personally, within a multicultural and international company. We also offer the following benefits:
- 40 working hours a week
- Modern working spaces
- Minimum 25 days of vacation
- Modern cafeteria spaces
- Monthly contribution to health insurance costs
- Training and development plans
- Free parking spaces as well as very good connections to public transportation
- Regular social company events such as summer party/winter party
If you want to contribute to the Evolution in visual freedom™ and become part of our passionate team, write us an email to send us your full application.
For more information, please reach out to our HR Team (032 33288 88) or visit us online at www.staar.com .