Associate Manager - Quality Assurance (Batch release)

Pfizer · Visakhapatnam

  • Experience8–10 yrs
  • SalaryNot disclosed
  • Work modeonsite
  • Posted29 Sept 2026

About Pfizer

Pfizer is hiring in Visakhapatnam in pharma biotech. This role looks for around 8+ years of experience.

Skills

  • pharmaceutical manufacturing quality
  • Good Manufacturing Practice
  • Good Documentation Practice
  • Microsoft Office
  • Microsoft Project
  • Statistical Software
  • audit management
  • sterile injectable manufacturing

The role

An associate quality assurance manager at a pharmaceutical manufacturing company ensures batch release through pharmaceutical manufacturing quality, Good Manufacturing Practice, and audit management, while applying Microsoft Office and SAP.

Full job description

Use Your Power for Purpose

Pfizer is driven by an unwavering commitment to delivering safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Your contributions will be vital and will have a direct impact on patient care, ensuring we deliver on our promise of quality and safety.

What You Will Achieve

In this role, you will:

Ensure that the electronic Batch Record/manual batch record Audit items are complete / approved per applicable policy/procedure. Ensure Expiration Date of the product/batch as per Marketing authorization specified. Ensure that all investigations are closed and disposition against the specified batches. Responsible for tracking of Quality restrictions/holds. Ensure adherence to Safety Procedures/GMP & GDP Practices. Interface with necessary plant disciplines to facilitate the accumulation, review, correction, and release of manufactured lots. Participate in and take responsibility for workplace environment, health and safety at the level required for this position, following the guidelines in the company Environmental, Health and Safety Management System Manual.

Here Is What You Need (Minimum Requirements)

B.Pharma, M.Pharma or MSC with 8-10 years of experience in Manufacturing Quality/Quality Control/ Production or in Quality Assurance of a pharmaceutical manufacturing facility. Sterile injectable experienceFundamental knowledge of basic work routines and standards sufficient to operate within narrow boundaries. Advanced/well-developed skills and knowledge within a specific professional discipline involving the integration of theory and principles with organizational practices and precedents. Excellent technical writing, communication, and presentation skillsProficiency in Microsoft Office, Microsoft Project, and Statistical SoftwareExperience in preparing and participating in audits and inspections

Bonus Points If You Have (Preferred Requirements)

Knowledge on SAP, gLIMS and AMPS. Strong analytical and problem-solving skillsAbility to work independently and as part of a teamStrong interpersonal skills and the ability to communicate effectively with all levels of the organizationAbility to adapt to changing priorities and manage multiple tasks simultaneouslyExperience in mentoring and training colleaguesExperience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Quality Assurance and Control