Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of protected and effective products to patients. Our versatile, innovative, 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.

By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy.

What You Will Achieve In this role, you will:
Create, review, and approve test method transfer and validation protocols, reports, and equipment qualification records.
Maintain compliance with Current Valuable Manufacturing Practices in Quality Control and Stability laboratories.
Support in investigations and critical assessments.
Change control process owner, tracking CAPA and BQ Metrics.
Manage Laboratory Information Management System builds, and review laboratory data.
Serve on cross-functional teams, conduct safety inspections, participate in audit walkthrough and responses,



recommend corrective actions, and train junior colleagues.

Here Is What You Need (Minimum Requirements)
M.Sc. Microbiology with 8+ years of industrial experience with any years of relevant experience
Strong technical skills in Change management, Risk management and Investigations.
Experience in microbiological testing and technical review.
Deep understanding of pharmaceutical manufacturing, packaging, and quality assurance operations
Detail-oriented with robust knowledge of quality systems
Effective written and verbal communication, as well as interpersonal skills

Bonus Points If You Have (Preferred Requirements)
Relevant pharmaceutical experience
Solid understanding of computer system utilization.
Experience with Laboratory Information Management Systems (LIMS)
Proficiency in data analysis and interpretation
Knowledge of regulatory requirements and guidelines
Strong problem-solving abilities
Effective time management and organizational skills
Ability to mentor and train junior colleagues

Work Location Assignment: On Premise

📌 Associate Manager Bq Qms And Compliance Visakhapatnam
🏢 Pfizer
📍 Visakhapatnam