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Associate- Microbiology

Pfizer
Pfizer
2-4 years
6-7 LPA
Chennai, India
10 April 27, 2026
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate – Microbiology (Quality Control / Quality Assurance)


Location: Visakhapatnam (Vizag), India (On-Site)
Company: Pfizer
Job ID: 4943934
Employment Type: Full-Time
Experience Required: Minimum 4+ years (Not suitable for freshers)


About the Company
Pfizer is a leading global biopharmaceutical organization committed to delivering safe, effective, and high-quality medicines worldwide. Driven by science, innovation, and compliance excellence, the company plays a critical role in improving patient outcomes through rigorous quality standards and continuous advancement.


Role Overview
The Associate – Microbiology role is a critical position within Quality Control and Quality Assurance functions, focusing on microbiological testing, compliance, and laboratory operations. This role directly contributes to ensuring product safety, regulatory adherence, and high-quality standards in pharmaceutical manufacturing.


Key Responsibilities

  • Prepare and maintain microbiological media, including sterilization using validated autoclave cycles

  • Handle Bio ball cultures, manage storage, and support Master culture maintenance and Cryo vial preparation

  • Perform microbiological testing such as water analysis, Microbial Limit Test (MLT), sterility testing, Bacterial Endotoxin Test (BET), Container Closure Integrity Testing (CCIT), and microbial challenge studies

  • Conduct sampling, labeling, and verification of materials, instruments, and laboratory equipment as per SOPs

  • Interpret microbiological data for accuracy, trends, and cGMP impact, recommending corrective and preventive actions

  • Maintain compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) in all documentation and quality records

  • Review, update, and revise Standard Operating Procedures (SOPs), analytical methods, and laboratory documentation

  • Perform analysis of finished products, raw materials, and components, including data entry, review, and approval in electronic systems

  • Generate Environmental Monitoring System (EMS) reports and support quality investigations

  • Collaborate with cross-functional teams to ensure timely completion of projects and adherence to quality timelines


Minimum Qualifications

  • Bachelor’s Degree or Associate Degree in Microbiology, Life Sciences, Pharmacy, or related field

  • Minimum 4+ years of hands-on experience in microbiology laboratory or pharmaceutical quality control

  • Strong technical expertise in microbiological testing and method validation

  • Ability to interpret compendial methods, SOPs, and regulatory guidelines

  • In-depth knowledge of GMP standards, laboratory compliance, and quality systems

  • Strong organizational, analytical, and multitasking skills

  • Effective written and verbal communication skills

  • Experience with quality control instruments and laboratory data management systems


Preferred Qualifications

  • Practical experience in microbiology laboratory techniques and aseptic practices

  • Exposure to continuous improvement initiatives such as Lean Manufacturing or Six Sigma

  • Strong understanding of statistical analysis and quality metrics

  • Problem-solving mindset with high attention to detail

  • Ability to manage multiple priorities in a regulated environment

  • Strong interpersonal skills and adaptability to evolving laboratory processes


Work Environment
On-site role based in Visakhapatnam, India, within a regulated pharmaceutical manufacturing and quality control environment.


Equal Opportunity Statement
Pfizer is an equal opportunity employer committed to fostering an inclusive and diverse workplace while complying with all applicable employment laws and regulations.


Important Note for Applicants
This role requires prior experience in microbiology and pharmaceutical quality control. Freshers are encouraged to apply for entry-level roles such as QC Microbiology Trainee, Quality Control Analyst, or Production roles to build relevant experience before applying to this position.


How to Apply
Apply through the official careers page or explore more verified global pharmaceutical job opportunities on ThePharmaDaily.com.