Full-time
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Technical Validation Director for Sterile Manufacturing
Posted by Jubilant Pharma, LLC • June 05, 2026
Description
Drive innovation in sterile manufacturing as Director of Validation. Use your technical acumen to ensure ongoing compliance and inspire teams during regulatory inspections.
In this influential role, you will act as the technical authority for the validation lifecycle. Your responsibilities include establishing governance frameworks while ensuring compliance with major regulatory bodies. With a focus on science-based decision-making, you will lead teams in maintaining high performance throughout validation activities.
Key Responsibilities:
• Define and execute validation governance strategies
• Manage validation plans, including engineering specifications
• Verify controlled validation states throughout production
• Oversee critical installations and equipment qualifications
• Ensure compliance in cleaning and sterilization validations
Requirements:
• Bachelor’s degree in engineering; microbiology courses are a plus
• 10-15 years of relevant validation expe...
In this influential role, you will act as the technical authority for the validation lifecycle. Your responsibilities include establishing governance frameworks while ensuring compliance with major regulatory bodies. With a focus on science-based decision-making, you will lead teams in maintaining high performance throughout validation activities.
Key Responsibilities:
• Define and execute validation governance strategies
• Manage validation plans, including engineering specifications
• Verify controlled validation states throughout production
• Oversee critical installations and equipment qualifications
• Ensure compliance in cleaning and sterilization validations
Requirements:
• Bachelor’s degree in engineering; microbiology courses are a plus
• 10-15 years of relevant validation expe...
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Submit your application today and take the next step in your career with Jubilant Pharma, LLC.
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