Key Responsibilities:

• Develop and implement validation protocols that adhere to cGMP and FDA regulations.
• Prepare and maintain comprehensive validation documentation and reports.
• Collaborate with various departments to address validation requirements and manage inspections effectively.

Requirements:

• Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related field.
• 1–3 years of relevant experience in pharmaceutical or nutraceutical manufacturing.

Job Type: Full-time | Work Location: On-site

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