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CROSS Research is looking for a Quality Assurance to join its Quality Assurance team. This position will collaborate with the Quality Assurance Manager to establish and ensure the quality of clinical studies conducted by CROSS Research. Responsibilities include:
Performing internal and external audits of clinical trials, documents, and subcontractors to ensure adherence to GCP, applicable regulations, and SOPs.
Supporting the management and organization of the company's Quality System, including preparation of SOPs, other quality documents, and management of training documentation.
Candidates who satisfy the following requirements may be preferred:
Degree in Biology, Pharmacy, Chemistry, or related disciplines.
Previous experience as Clinical Monitor, Auditor, Quality Assurance, or Regulator.
Basic analytical experience to support laboratory audits.
Fluent in English and capable of independently preparing technical documents and reports.
Strong practical and theoretical computer skills, with an aptitude for quickly learning new IT systems and technologies.
Availability to travel regularly for audit activities.
The main place of work will be Mendrisio, Switzerland, with activities also performed at other sites; own car is required. This is a full-time on-site position (40 hours/week). A challenging opportunity in a small, dedicated team is offered.
Note: Unsatisfactory candidates will not receive a response.
Seniority level Entry level
Employment type Full-time
Job function Quality Assurance
Industries Research Services
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