CSV Validation Specialist

il y a 3 semaines


Toulouse, Occitanie, France Optimus Life Sciences Temps plein

Job Title: CSV Validation Specialist


We are seeking an experienced CSV Validation Specialist to join our team at Optimus Life Sciences. As a CSV Validation Specialist, you will be responsible for ensuring the validation of computerized systems in the biopharmaceutical industry.


Responsibilities:

  • Validate computerized systems to ensure compliance with GMP regulations
  • Develop and implement validation plans and protocols
  • Conduct risk assessments and identify potential validation risks
  • Collaborate with cross-functional teams to ensure validation activities are completed on time and within budget
  • Develop and maintain validation documentation and records
  • Stay up-to-date with industry regulations and trends


Requirements:

  • 5-10 years of experience in CSV validation
  • Experience working in the biopharmaceutical industry under GMP regulations
  • Strong understanding of GMP regulations and industry standards
  • Excellent communication and collaboration skills
  • Fluent in English


About Optimus Life Sciences:

Optimus Life Sciences is a leading company in the biopharmaceutical industry. We are committed to delivering high-quality products and services to our clients. Our team is passionate about innovation and excellence, and we are seeking like-minded individuals to join our team.


How to Apply:

If you are interested in this role, please submit your CV and a cover letter to us. We look forward to hearing from you


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