Our client is actively seeking a skilled QA CSV Specialist to join their dynamic team. If you're passionate about Computer System Validation (CSV) in a biotech setting and possess a keen eye for quality, this is your opportunity to contribute to cutting-edge biotechnological breakthroughs.
- Lead and execute CSV activities for critical systems within the biotech environment.
- Develop and implement CSV strategies, protocols, and procedures in alignment with regulatory requirements and industry best practices.
- Collaborate closely with cross-functional teams to ensure seamless integration of CSV processes into system development life cycles.
- Conduct risk assessments and implement risk mitigation strategies related to CSV activities.
- Drive continuous improvement initiatives to enhance the efficiency and effectiveness of CSV processes.
- Provide expertise during regulatory inspections and audits related to CSV.
- Bachelor's or advanced degree in a relevant scientific or technical discipline.
- Proven experience in Computer System Validation within the biotech or pharmaceutical industry.
- In-depth knowledge of regulatory requirements and guidelines for CSV in a GxP environment.
- Strong analytical, problem-solving, and documentation skills.
- Excellent communication and collaboration abilities.
- Familiarity with automation systems and data integrity considerations.
- Fluency in English; additional language proficiency is a plus.
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