HomeProductionMicrobiologySenior Executive - Microbiology | Pfizer Ltd | Vizag

Senior Executive – Microbiology | Pfizer Ltd | Vizag


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The global Pfizer leadership is making efforts to make the company lean and agile. Employees are encouraged to be innovative and entrepreneurial. We are also working to create an environment where all colleagues have the opportunity to grow and maximize their contributions to the company’s success.

Pfizer is a Fortune 500 company that embraces the spirit of a small company while exploiting the advantages of its unmatched scale and reach.

Position: Sr. Executive – Microbiology

Location: Vizag, Andhra Pradesh, India

Job Description:

Why Patients Need You

Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.  Our science and risk-based compliant quality culture are flexible, innovative, and customer-oriented. Whether you are involved in the development, maintenance, compliance, or analysis through research programs, your contribution will directly impact patients.

What You Will Achieve

  • You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. Your knowledge of quality control will be helpful to support our quality programs.
  • Your ability to analyze chemical, biological or microbiological products will help us manage our quality.
  • Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification, and sterility testing will help Pfizer provide safe drugs to its patients.
  • Your qualifications of unique Quality Control instruments will help us meet accuracy specifications for sample management, retains management, interpretation and evaluation.
  • You will also be relied on for establishing requirements for the transfer of methodology from R&D.
  • As an associate, your focus on the job will contribute in achieving project tasks and goals.
  • Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
  • It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

  • Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
  • Lead efforts to improve process performance, procedures and reporting to meet changing quality and regulatory compliance.
  • Able to create, review, and approve compliant test method transfer and validation protocols and reports and equipment qualification/computer validation records.
  • Perform tasks associated with maintaining Current Good Manufacturing Practices {part of GxP} compliant Quality Control and Stability laboratories.
  • Support preparation of media, receipt, storage and handling of Bio ball cultures, and investigations related to microbiology.
  • Perform testing including, but not limited to clinical and/or commercial product, raw materials, validation, stability, and Environment Monitoring samples.
  • Support detailing requirements for Laboratory Information Management System builds, building, testing and managing its Master Data changes.
  • Review and authorize all laboratory data and have an extensive overall knowledge of all laboratory operations.
  • Serve on cross functional teams to represent Quality Control and facilitate communications and activities/projects
  • Perform safety inspection of laboratories and surrounding office area as assigned and prepare a report.
  • Participate in out-of-specification and failure investigations and recommend corrective actions and demonstrate problem solving abilities.
  • Train junior colleagues and may develop training plans and/or oversee training activities for groups.



  • Master’s Degree in Biological Science
  • 5+ years’ experience
  • Technical Skills Experience in ML T method validation and testing
  • Experience in microbiological testing of water
  • Understanding of pharmaceutical manufacturing, packaging, and quality assurance operations
  • Detail oriented with Quality systems knowledge
  • Knowledge of research unit clinical and analytical Laboratory environment
  • Excellent effective written and verbal communication and interpersonal skills
  • Ability to work in a team environment


  • Master’s degree
  • Relevant pharmaceutical experience
  • Knowledge of computer system hardware, infrastructure and networks

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