Pfizer Hiring QA,QC

Pfizer QA QC Jobs Visakhapatnam Pharma Hiring

Pfizer hiring for QA and QC roles in Visakhapatnam. B.Pharm, M.Sc candidates with 2–8 yrs pharma experience apply now.

Pfizer Healthcare India Private Limited is hiring experienced professionals for multiple Quality Assurance (QA) and Quality Control (QC) roles at its Visakhapatnam facility. This is a premium opportunity for candidates looking for pharmaceutical QA jobs, analytical QC careers, microbiology quality control positions, and regulatory compliance roles in a globally recognized pharmaceutical company.

Professionals with expertise in analytical testing, cGMP compliance, method validation, quality systems, and injectable manufacturing can build long-term careers in one of the world’s most respected healthcare organizations. These openings are especially valuable for candidates aiming to work in regulated pharmaceutical environments with exposure to global quality standards.

Company Overview

Pfizer is one of the world’s leading pharmaceutical and biotechnology companies, known for delivering breakthrough medicines and innovative healthcare solutions. The company operates globally with a strong focus on research, quality systems, regulatory compliance, and patient safety.

Pfizer’s Visakhapatnam facility plays an important role in pharmaceutical manufacturing and quality operations. Working at Pfizer provides professionals with exposure to international regulatory standards including cGMP, Good Laboratory Practices (GLP), quality risk management systems, and pharmaceutical compliance management.

The company’s commitment to innovation and quality assurance makes it one of the most preferred employers for pharmaceutical, microbiology, and biotech professionals.

Job Role & Responsibilities

Pfizer is hiring for multiple positions across Quality Control and Quality Assurance functions.

Associate – Quality Control (Injectables)

Key Responsibilities

• Perform analytical method transfers, method validation, and method verification activities
• Conduct analytical testing using complex laboratory techniques
• Interpret laboratory data for accuracy, precision, and cGMP impact
• Review and revise SOPs, analytical methods, and quality documents
• Perform analysis of raw materials, finished products, and components
• Ensure compliance with GMP and GLP documentation standards
• Support laboratory investigations and corrective action processes

Associate Manager – Quality Assurance

Key Responsibilities

• Review clinical and commercial drug batches for compliance
• Perform sampling and statistical process control activities
• Approve investigations and change control activities
• Assess quality impact and cGMP compliance risks
• Ensure manufacturing and packaging quality standards are maintained
• Support project execution and quality documentation management

Associate Manager – Quality Control (QC)

Key Responsibilities

• Create and approve method transfer and validation protocols
• Maintain compliance within QC and stability laboratories
• Support microbiology-related investigations and media preparation
• Handle Laboratory Information Management System (LIMS) activities
• Conduct laboratory testing and data review processes
• Train junior colleagues and participate in quality investigations

Associate – Quality Assurance (QA)

Key Responsibilities

• Evaluate product and process quality documents
• Review manufacturing and packaging quality compliance
• Identify and manage deviations from established standards
• Support investigations and change control processes
• Ensure compliance with pharmaceutical quality systems and cGMP standards

These responsibilities directly contribute to patient safety, pharmaceutical product quality, and regulatory compliance in global healthcare manufacturing.

Eligibility / Qualifications

Associate – Quality Control (Injectables)

• Bachelor’s Degree in Chemistry or Microbiology with 4–5 years of analytical testing experience
  OR
• Master’s Degree in Chemistry or Microbiology with 2–3 years of analytical testing experience

Associate Manager – Quality Assurance

• Bachelor’s Degree in Science or Pharmacy with 6–8 years of pharma/biotech experience
  OR
• Master’s Degree in Science or Pharmacy with 5–7 years of pharma/biotech experience

Associate Manager – Quality Control

• Master’s Degree in Chemistry or Microbiology with 5–7 years of analytical testing experience

Associate – Quality Assurance

• Bachelor’s Degree in Science or Pharmacy with 4–5 years of pharma/biotech experience
  OR
• Master’s Degree in Science or Pharmacy with 2–3 years of pharma/biotech experience

Relevant Courses

B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Microbiology, M.Sc Biotechnology, Pharmaceutical Analysis, Quality Assurance, Regulatory Affairs

Required Skills

• Analytical testing and method validation expertise
• Knowledge of cGMP, GLP, and pharmaceutical compliance management
• Experience with HPLC, laboratory systems, and QC documentation
• QA investigation handling and change control management
• Sterile injectable manufacturing and microbiology knowledge
• Regulatory compliance and audit readiness skills

Location & Salary

Job Location: Pfizer Healthcare India Private Limited, Visakhapatnam

Salary: Competitive pharmaceutical QA/QC salary package based on qualification, technical expertise, and regulatory experience

Professionals with expertise in injectable manufacturing, quality systems, and analytical testing are among the highest-demand talent categories in the pharmaceutical and biotech sectors.

Application Process

Interested and qualified candidates can share their updated CV to:

Email: IOANNA.ZOURELIDOU@pfizer.com

Applicants should ensure that their resume highlights experience in analytical testing, quality systems, regulatory compliance, investigations, and pharmaceutical documentation.

Why This Opportunity Matters

Quality Assurance and Quality Control are among the most important and highest-paying domains in pharmaceutical manufacturing because they directly impact product quality, regulatory approvals, and patient safety.

Professionals with expertise in analytical testing, method validation, injectable quality systems, and pharmaceutical compliance management are highly valued globally. Experience with Pfizer significantly enhances professional credibility and opens pathways into senior regulatory, validation, and quality leadership roles.

Working in regulated pharmaceutical environments also improves expertise in global audit readiness, change management systems, laboratory compliance, and risk-based quality operations.

Key Highlights

• Company: Pfizer Healthcare India Private Limited
• Departments: Quality Assurance, Quality Control
• Roles: Associate, Associate Manager
• Qualification: B.Pharm, M.Pharm, M.Sc
• Experience: 2–8 Years
• Industry: Pharma / Biotech / Injectables
• Location: Visakhapatnam

FAQs

Who can apply for Pfizer QA/QC jobs?

Candidates with B.Pharm, M.Pharm, M.Sc Chemistry, or Microbiology qualifications and relevant pharma experience can apply.

What experience is required?

Candidates should have 2 to 8 years of experience in pharma, biotech, analytical testing, QA, or QC operations.

What technical skills are preferred?

Method validation, analytical testing, cGMP compliance, investigations, LIMS, injectable quality systems, and microbiology testing.

Are injectable manufacturing skills preferred?

Yes, candidates with injectable manufacturing and sterile compliance experience are highly preferred.

How can I apply?

Interested candidates can apply by sending their updated CV to the official Pfizer recruitment email.

Summary Table

|———————————-|———————————-|
| Company | Pfizer Healthcare India Pvt. Ltd. |
| Vacancies | Associate QA, Associate QC, Associate Manager QA/QC |
| Required Education | B.Pharm, M.Pharm, M.Sc |

Experience	2–8 Years