Microbiology Job Vacancy at Pfizer
Looking for Microbiology Jobs in the pharmaceutical industry? Here’s an exciting opportunity from Pfizer Jobs for the position of Associate – Microbiology at its Vizag facility. If you have a background in Microbiology, Biotechnology, Life Sciences, Pharmacy, or related disciplines and are eager to build a rewarding career in quality control and microbiological testing, this Life Science Jobs opening could be the perfect next step. Explore eligibility, responsibilities, required skills, and application details below before the opportunity closes.
About Pfizer
Pfizer is one of the world’s leading biopharmaceutical companies dedicated to discovering, developing, manufacturing, and delivering innovative medicines and vaccines. Operating in more than 180 countries, Pfizer focuses on improving patient health through scientific innovation, quality manufacturing, and regulatory excellence. The company’s India operations offer outstanding career opportunities across research, manufacturing, quality control, microbiology, regulatory affairs, and other Life Science Jobs, making Pfizer Jobs highly sought after by life science professionals.
Job Details
- Job Title: Associate – Microbiology
- Location: Vizag, India
- Time Type: Full time
- Job Requisition ID: 4960404
Position Overview
The Associate – Microbiology is responsible for performing microbiological testing, laboratory operations, and quality control activities to ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). The role supports the production of safe and effective pharmaceutical products through accurate testing, documentation, data analysis, and adherence to regulatory standards. The associate works under the guidance of supervisors while contributing to laboratory efficiency, quality assurance, and continuous improvement initiatives.
Key Responsibilities
- Assists in the preparation and maintenance of microbiological media stocks, including sterilization of laboratory accessories using autoclave cycles.
- Manages the receipt, storage, and handling of BioBall cultures and supports the maintenance of master cultures and preparation of cryovials.
- Performs routine microbiological analyses, including water testing, Microbial Limit Tests (MLT), Sterility Testing, Bacterial Endotoxin Tests (BET), Container Closure Integrity Testing (CCIT), and microbial challenge studies.
- Conducts sampling, labeling, and verification of materials, laboratory equipment, and analytical instruments according to established procedures.
- Interprets and evaluates analytical data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective and preventive actions when required.
- Maintains accurate laboratory documentation and quality records in compliance with GMP, GLP, and regulatory requirements.
- Reviews, updates, and revises Standard Operating Procedures (SOPs), analytical methods, and related laboratory documentation.
- Performs quality control analyses on finished products, raw materials, and packaging components.
- Enters, reviews, and approves laboratory data within computerized quality management systems and generates Environmental Monitoring System (EMS) reports.
- Maintains training records to ensure personnel competency and compliance with laboratory qualification requirements.
- Supports project execution by planning work activities, managing priorities, and meeting established timelines under supervisory guidance.
- Collaborates with cross-functional teams to ensure laboratory operations meet quality, safety, and compliance standards.
Required Qualifications
- Bachelor’s degree in a relevant scientific discipline, or
- Associate’s degree with four years of relevant laboratory experience, or
- High school diploma (or equivalent) with six years of relevant laboratory experience.
Technical Skills
- Knowledge of microbiological laboratory techniques and quality control testing.
- Experience in microbiological analyses, including water testing, sterility testing, microbial limit testing, bacterial endotoxin testing, CCIT, and environmental monitoring.
- Understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and applicable regulatory requirements.
- Ability to interpret pharmacopeial methods, Standard Operating Procedures (SOPs), technical documents, and regulatory guidelines.
- Proficiency in laboratory instrumentation, sample management, data interpretation, and computerized laboratory systems.
- Strong documentation practices and regulatory compliance awareness.
Preferred Skills
- Experience with analytical laboratory techniques, particularly High-Performance Liquid Chromatography (HPLC).
- Knowledge of Lean Manufacturing principles, Six Sigma methodologies, and statistical analysis.
- Experience leading or contributing to continuous improvement initiatives.
- Familiarity with Environmental Monitoring Systems (EMS) and computerized laboratory databases.
- Experience using AI-powered productivity tools such as ChatGPT or Microsoft Copilot while adhering to responsible AI practices and ethical guidelines.
Core Competencies
- Strong analytical and problem-solving abilities.
- High attention to detail and commitment to data integrity.
- Excellent organizational and time management skills.
- Ability to manage multiple priorities while meeting deadlines.
- Effective written and verbal communication skills.
- Strong interpersonal and teamwork abilities.
- Adaptability, continuous learning mindset, and willingness to adopt new laboratory technologies and procedures.
- Commitment to quality, regulatory compliance, and patient safety.
