Associate Manager - MQA Downstream

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Associate – Equipment Maintenance

Pfizer

In OfficeVisakhapatnam

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Skills you'll use

What you'll do

• Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations.
• Maintain regulatory compliance in accordance with cGMP practices
• Ensure manufacturing policies and procedures conform to Pfizer standards
• Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Team leader.
• Review of Batch reports, and Equipment audit trails.
• Hands on Inspector qualification and defect kit management activities.

Who can apply

• Preferred Education/ Qualification
• B. Pharm, M. Pharm, MSc.
• Here Is What You Need (Minimum Requirements)
• 6-8 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility.
• Strong facilitation skills combined with instructional systems design experience
• Excellent interpersonal and communication skills to build and maintain effective working partnerships across all levels of the organization
• Proven ability to lead complex projects to successful outcomes
• Excellent computer skills, including proficiency in Microsoft Office Suite
• Ability to manage and assess vendors who develop and conduct training programs for the manufacturing team
• Bonus Points If You Have (Preferred Requirements)

About Pfizer

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