Our client is a prominent biotech company at the forefront of groundbreaking developments in immunotherapy. They are seeking a highly skilled and dedicated QA Systems Specialist to join their team in Switzerland.
- System Oversight: Manage and maintain the Quality Assurance systems, including Quality Management Systems (QMS), document control, and training systems.
- Compliance Assurance: Ensure that all quality management systems are in compliance with relevant regulatory standards, such as GxP, ISO, and FDA requirements.
- Documentation Control: Oversee document control procedures, including document creation, review, approval, distribution, and archiving.
- Continuous Improvement: Collaborate on the development and improvement of quality processes and systems, identifying areas for enhancement and optimization.
- Audits and Inspections: Support internal and external audits and inspections related to quality management systems.
- Risk Management: Implement and maintain risk management processes to ensure proactive identification and mitigation of quality risks.
- Bachelor's degree in a related field, such as Life Sciences or Quality Management.
- Proven experience in managing Quality Assurance systems, ideally within the biotech or pharmaceutical industry.
- Strong knowledge of regulatory requirements, including GxP, ISO, and FDA standards.
- Proficiency in using QMS and document control systems.
- Excellent communication and interpersonal skills.
- A proactive and detail-oriented approach to work.
- Fluent in English and French; additional language skills are a plus.
- Strong problem-solving skills and the ability to work collaboratively.
Can this be interesting for you or anyone you know? If so, please apply here or contact Conor Kelly with your number/CV ASAP and he will give you a call.
?: +41 (0) 44 5514 407