Job Summary
The successful candidate will be responsible for ensuring compliance with cGMP, BPD, and EHS standards in a quality control environment. They will conduct routine and non-routine quality control activities, manage deviations, and propose solutions for complex technical issues.
Key Responsibilities
1. Compliance and Quality Control: Adhere to regulatory standards, perform quality control activities, and oversee equipment maintenance.
2. Deviations and CAPA: Initiate and handle deviations, ensuring proper implementation of corrective actions.
3. Technical Problem Solving: Identify, propose, and resolve complex technical issues related to biochemical methods and technology.
4. Training and Knowledge Sharing: Train analysts on QC methods, systems, and equipment, and share expertise on laboratory techniques.
5. Continuous Improvement: Develop and implement process improvements, collaborating with QC Sciences on projects and initiatives.
6. Collaboration and Support: Work with the quality control team on regulatory submissions and harmonization projects, providing subject matter expertise as needed.
Requirements
* Solid laboratory experience, including biochemical methods such as HPLC, ELISA, enzyme activity, Western blot, etc.
* CFC in laboratory / biology or other relevant scientific field (minimum level of education).
* Minimum 3 years' experience in a QC laboratory in a cGMP environment for a junior position, 5 for a senior position.
* Desirable: Experience in HPLC electrophoresis, Elisa or enzyme activity determination.
* Fluent French and technical English language skills.
* Eligibility: Swiss or EU nationality, or valid Swiss work permit.
About the Opportunity
* A six-month contract with an internationally known biotechnology company.
* An opportunity to develop your career in a dynamic and innovative environment.