Pfizer Microbiology Job Opening – Online Application Process

Pfizer Microbiology Job

Pfizer Microbiology Job Opening – Online Application Process

Pfizer Microbiology Job Opening – Online Application Process. Pfizer is hiring candidates for an Associate Manager (Microbiology) vacancy. Interested and eligible applicants can check out all of the details on the same below –

Job Title – Associate Manager (Microbiology)

Job ID – 4859284

Location of Pfizer Vacancy – India – Vizag

What You Will Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients.

Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D.

As a Senior Associate, your knowledge and skills will contribute to the goals and objectives of the team.  Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate explaining difficult issues and establishing consensus between teams


It is your hard work and commitment that will make 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 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
  •  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 in Microbiological test validation and testing procedure.

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