Urgent Pfizer Hiring Associate Quality Control | M.Pharm & MSc Apply

Pfizer is hiring experienced professionals for the position of Associate – Quality Control at its Vizag manufacturing facility. This opportunity is ideal for candidates with expertise in analytical method validation, method transfer, GMP-regulated laboratory operations, quality control testing, and pharmaceutical analytical sciences.

Professionals seeking careers in Quality Control, Analytical Research, Method Validation, Pharmaceutical Testing, GMP Compliance, and Regulatory Laboratory Operations can explore this exciting opportunity with one of the world’s leading pharmaceutical companies.

Company Overview

Pfizer is a globally recognized biopharmaceutical company committed to discovering, developing, and delivering innovative medicines and vaccines that improve patient health worldwide. The company operates advanced manufacturing and research facilities across multiple countries and is known for maintaining the highest standards of pharmaceutical quality, compliance, and scientific excellence.

Pfizer’s Quality Control teams play a critical role in ensuring that medicines meet stringent regulatory, safety, and quality standards before reaching patients.

Job Role & Responsibilities

Analytical Method Validation & Transfer

• Perform analytical method validation activities as per approved protocols.
• Execute analytical method transfer and method verification studies.
• Support new product introduction (NPI) projects through analytical assessments.
• Conduct method gap assessments against pharmacopeial requirements.
• Ensure compliance with ICH, USP, EP, and regulatory standards.

Quality Control Testing

• Perform testing of raw materials, finished products, and packaging components.
• Execute analytical evaluations using validated methods.
• Review and interpret analytical data.
• Ensure accurate recording and reporting of laboratory results.
• Support batch release testing activities.

Instrument Operation & Laboratory Analysis

• Operate advanced analytical instruments.
• Perform routine and specialized laboratory testing.
• Ensure instruments meet calibration and performance requirements.
• Support troubleshooting and laboratory investigations.

Documentation & Compliance

• Maintain documentation in compliance with Good Manufacturing Practices (GMP).
• Follow Good Laboratory Practices (GLP) requirements.
• Review and revise Standard Operating Procedures (SOPs).
• Maintain quality records and laboratory documentation.
• Support audit and inspection readiness activities.

Data Analysis & Continuous Improvement

• Analyze trends and identify potential quality risks.
• Evaluate analytical results for accuracy and precision.
• Recommend corrective and preventive actions where required.
• Participate in continuous improvement and laboratory excellence initiatives.

Eligibility / Qualifications

Educational Qualification

Candidates must possess:

• M.Sc Chemistry
• M.Pharm

Eligible Specializations

M.Sc Analytical Chemistry, M.Sc Organic Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Applied Chemistry, M.Sc Medicinal Chemistry, M.Pharm Pharmaceutical Analysis, M.Pharm Quality Assurance, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Chemistry, M.Pharm Drug Regulatory Affairs, and related specializations.

Experience Required

• 2 to 5 years of relevant pharmaceutical Quality Control experience.
• Experience in Analytical Method Transfer and Method Validation is mandatory.
• Experience in GMP-regulated pharmaceutical laboratories preferred.

Required Skills

Quality Control & Analytical Skills

• Analytical Method Validation
• Analytical Method Transfer
• Method Verification
• Pharmaceutical Quality Control
• Stability Testing
• Laboratory Investigations

Instrumentation Expertise

Candidates should be qualified in multiple analytical techniques, including:

• HPLC (High Performance Liquid Chromatography)
• GC (Gas Chromatography)
• UV-Visible Spectroscopy
• FTIR
• Karl Fischer Titration
• pH Meter Analysis

Regulatory & Compliance Knowledge

• ICH Q2 (R1/R2)
• USP Standards
• EP Standards
• BP Standards
• JP Standards
• GMP Compliance
• GLP Compliance
• Data Integrity Requirements

Professional Skills

• Analytical Thinking
• Problem Solving
• Documentation Management
• Time Management
• Communication Skills
• Attention to Detail
• Cross-Functional Collaboration

Location & Salary

Location: Visakhapatnam (Vizag), Andhra Pradesh

Salary: ₹6.5 LPA – ₹11 LPA (Approximate Industry Standard Based on Experience and Technical Expertise)

Application Process

Interested candidates can apply through the official Pfizer Careers portal.

Apply Here:

Frequently Asked Questions (FAQs)

1. What qualifications are required for the Associate Quality Control role?

Candidates with M.Sc Chemistry or M.Pharm qualifications are eligible.

2. How much experience is required?

Applicants should have 2–5 years of experience in Quality Control, particularly in method validation and method transfer activities.

3. Which analytical instruments should candidates be familiar with?

Candidates should have experience with HPLC, GC, UV-Vis, FTIR, Karl Fischer titration, and pH meters.

4. Is knowledge of ICH guidelines required?

Yes. Candidates should have working knowledge of ICH Q2, USP, EP, BP, and JP requirements.

5. What type of projects will the selected candidate support?

The role involves analytical method validation, method transfer, quality control testing, and new product introduction activities.

6. Where is the job located?

The position is based in Visakhapatnam (Vizag), Andhra Pradesh.

Job Summary