Job Description & How to Apply Below
Your role will focus on advancing commissioning and qualification processes within the pharmaceutical industry.
As a skilled CQV Engineer, you'll ensure all compliance measures are met while supporting diverse projects. You'll independently manage C&Q documentation, review critical technical documents, and provide solutions for any validation discrepancies. Your contributions will help maintain the rigorous standards expected in healthcare and pharmaceutical manufacturing.
Key Responsibilities:
• Provide services to site management for C&Q initiatives
• Review and ensure accuracy of commissioning documentation
• Participate actively in validation project phases
• Support troubleshooting and resolutions for validation issues
• Offer recommendations for qualified systems acceptance
Requirements:
• Bachelor's degree in a relevant technical field
• 2-5 years of CQV experience in pharmaceuticals or biotech
• Hands-on skills in validation and compliance
• Understanding of cGMP guidelines
• Capability to address validation deviations
Enhance your career while supporting high-standard healthcare products at Pharm Eng Technology.
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