Commissioning & Validation Engineer - Pharmaceutical Manufacturing

5 days ago


London, Greater London, United Kingdom Consultys Full time
About Consultys

We are a global engineering and services consulting company dedicated exclusively to the Life Sciences industry. Our team of 750 consultants works on innovative activities in engineering, production, quality (QA, QC, validation), R&D, and regulatory affairs across various regions.

Job Summary

We are seeking an experienced Commissioning, Qualification, and Validation (CQV) Engineer to join our team. The CQV Engineer will play a crucial role in ensuring that all systems and equipment are properly commissioned, qualified, and validated according to industry standards and regulatory requirements.

Key Responsibilities
  1. Lead CQV activities for pharmaceutical manufacturing projects, ensuring compliance with industry regulations and standards.
  2. Develop and execute commissioning, qualification, and validation protocols, collaborating with cross-functional teams.
  3. Conduct risk assessments and develop mitigation strategies to ensure the successful implementation of CQV activities.
  4. Document and report on CQV activities, findings, and corrective actions, supporting continuous improvement initiatives.
Requirements
  1. Bachelor's or Master's degree in Engineering or a related field.
  2. Minimum of 5 years of industrial experience in CQV roles, with at least 2 years in the pharmaceutical industry.
  3. Strong understanding of industry regulations and standards, such as cGMP and FDA guidelines.
  4. Excellent analytical and problem-solving skills, with effective communication and interpersonal skills.
  5. Ability to work effectively within cross-functional teams, supporting the company's mission and values.

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