CQV Engineer
Job Description & How to Apply Below
Drive commissioning and qualification activities as a CQV Engineer with Pharm Eng Technology. This role emphasizes independent validation work, supporting technical management across various projects involving equipment and facilities.
As a key player, you will work with Technical Services management to increase throughput and efficiency in C&Q activities. The role involves reviewing documentation for compliance with regulatory standards and participating in all phases of validation projects. Your expertise will aid in resolving issues related to equipment, cleaning, and validation deviations.
Key Responsibilities:
• Provide direct services to Technical Services management
• Validate commissioning and qualification documentation for accuracy
• Review technical documents for compliance and validation principles
• Support investigations and troubleshooting efforts
• Offer effective solutions for system deviations and non-conformances
Requirements:
• Bachelor’s degree in engineering, biology, chemistry, or pharmacy
• 2-5 years of technical experience in CQV
• Hands-on experience in validation disciplines
• Strong knowledge of cGMP requirements
• Ability to work independently and collaboratively
Utilize your CQV expertise at Pharm Eng Technology to enhance project success and regulatory compliance.
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