Join a dynamic team as a Senior Process Engineer, supporting capital projects with technical oversight of Commissioning, Qualification, and Validation (CQV) activities in a regulated pharmaceutical environment.
Our Client is looking for a qualified Senior Process Engineer to ensure compliance and maintain inspection readiness. You will utilize your expertise in GMP principles and risk-based methodologies to oversee CQV documentation and strategy. This role emphasizes compliance with regulatory standards while supporting project delivery effectively.
Key Responsibilities:
- Provide oversight on CQV documentation including risk assessments
- Translate process requirements into GMP-compliant strategies
- Identify critical quality attributes and process parameters
- Apply risk assessments for qualification and testing scope
- Review and approve CQV lifecycle documentation
Requirements:
- Bachelor's degree in Engineering (Chemical, Mechanical, Electrical)
- At least 5 years' experience in CQV in a pharmaceutical setting
- Strong knowledge of pharmaceutical manufacturing processes
- Familiar with GMP regulations and ICH guidelines
- Excellent stakeholder management and communication skills
Leverage your CQV expertise and compliance knowledge to drive successful project outcomes with our Client.
Senior Process Engineer for CQV Activities in Lunenburg employer: DPS Group Global
Join a forward-thinking company that prioritizes innovation and sustainability in wastewater treatment solutions. With a strong emphasis on collaboration and safety, employees are encouraged to grow professionally through mentorship opportunities and hands-on project involvement. Located in a vibrant community, this role offers a unique chance to make a meaningful impact while working alongside passionate professionals dedicated to excellence.
