Pfizer

Associate Microbiology

Posted 2 Days Ago

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Vizag, Vishākhapatnam, Andhra Pradesh, IND

In-Office

Senior level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Support microbiology QC testing and documentation under cGMP/GLP: prepare media, maintain cultures, run sterility, endotoxin, water and CCIT tests, sample and label materials, analyze data, update SOPs, enter and review results in computerized systems, and contribute to projects under supervisor direction.

Summary Generated by Built In

Use Your Power for Purpose
Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard.
What You Will Achieve
In this role, you will:

Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles.
Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials.
Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies.
Ensure training records are updated and correctly filed to reflect current testing capabilities.
Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.
Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.
Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.
Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.
Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.

Here Is What You Need (Minimum Requirements)

Master's degree (Microbiology / Bio-technology) with 4-5 years of experience and relevant experience
Demonstrated technical skills in method validation and testing
Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
Knowledge of Good Manufacturing Practices and its application standards, processes, and policies.
Excellent organizational skills and strong ability to multi-task
Strong written and verbal communication skills
Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Bonus Points If You Have (Preferred Requirements)

Proven track record in leading continuous improvement projects
Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis
Strong problem-solving skills and attention to detail
Ability to manage multiple priorities and meet deadlines.
Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
Adaptability and willingness to learn new techniques and procedures
Experience 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

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

Skills Required

Master's degree in Microbiology or Biotechnology with 4-5 years of relevant experience
Demonstrated technical skills in method validation and testing
Ability to read and understand compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
Knowledge of Good Manufacturing Practices (cGMP) and its application standards, processes, and policies
Excellent organizational skills and strong ability to multi-task
Strong written and verbal communication skills
Proficiency with Quality Control instruments for sample management, retention management, interpretation, and evaluation

What the Team is Saying

Pfizer Compensation & Benefits Highlights

Healthcare Strength — Official materials describe comprehensive medical, dental, vision, and mental-health support, plus fertility/family‑building and transgender‑inclusive coverage; eligible Pfizer medications are noted as available at no cost in U.S. plans. Wellness resources such as telehealth and preventative programs are also emphasized.
Retirement Support — Company documents highlight a 401(k) with matching contributions plus an additional Retirement Savings Contribution beyond the match. Financial planning support and company‑paid life and disability insurance further bolster long‑term security.
Leave & Time Off Breadth — Corporate pages and job postings describe paid vacation and holidays, caregiver leave, and paid parental leave for both parents. Materials also note that details can vary by role and location.

Learn more about Pfizer's Compensation & Benefits →

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.