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