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Pfizer
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Associate Manager - Validations

Associate Manager - Validations

Pfizer

4 - 7 years

6 - 10 Lacs

Visakhapatnam

Posted:14 hours ago| Platform:

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Skills Required

Medical devices Data analysis Manager Quality Assurance Compliance Analytical Pharma Quality systems New product development Document management system Auditing

Work Mode

Work from Office

Job Type

Full Time

Job Description

Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care.

What You Will Achieve

In this role, you will:

Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.
Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution.
Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations.
Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards.
Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.
Manage routine Quality systems such as Change Control, Quality Agreement, Documentation, and Investigations, and coordinate testing with functional groups.
Maintain the Site Validation Master Plan, support regulatory audits, and represent engineering validation on site or network teams.
Support product transfers, new product development, regulatory queries, cost improvement projects, and Cleaning Validation, ensuring integration of validation schedules in production and participating in deviation investigations.

Here Is What You Need (Minimum Requirements)

High school diploma (or equivalent) with 8+ years of experience or associate s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience
Proven expertise in Good Manufacturing Practices
Strong working knowledge of various quality systems and processes
Familiarity with information systems such as Global Document Management System, System Application & Products, and Quality Tracking System
Excellent verbal and written communication skills
Ability to work independently and in a team environment

Bonus Points If You Have (Preferred Requirements)

Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems
Experience with sterile products and medical devices
Strong analytical and problem-solving skills
Strong organizational and time management skills
Ability to mentor and guide other colleagues
Experience in regulatory audits and compliance

Quality Assurance and Control

#LI-PFE

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Associate Manager - Validations