Pfizer Microbiology Investigation Lead
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Pfizer Microbiology Investigation Lead Job – Apply Online

Pfizer Microbiology Investigation Lead Job – Apply Online. Pfizer is hiring Microbiology candidates for Investigation Lead – Microbiology vacancy. Interested and eligible applicants can check out all of the details on the same below:

Pfizer Vacancy Details

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Job Title: Investigation Lead – Microbiology

Job ID: 4784431

Location of Pfizer Vacancy: India – Vizag

Job Description:

  • To ensure the lab functions are in line with the current cGMP requirements. To guarantee compliance with quality/ safety/cGMP procedures.
  • To support regulatory, corporate and customer (if applicable) audits and to provide timely response and compliance to the audit findings.
  • To participate in corporate discussions on Microbiology related activities and provide an overview of the site procedures.
  • To provide necessary resources for smooth and timely execution of analysis and lab functions.
  • To identify the manpower needs and to recruit the people with adequate competencies.
  • To induct the new joiners as per the procedures.
  • To guarantee adherence to Excellent Documentation Practices. To monitor documentation errors and to create awareness among the teams via training and periodic interactions for minimization of the same.
  • To review investigations for their adequacy and to recommend additional investigation areas if not adequate. Additionally to develop and implement effective CAPA’s.
  • Review, approve and implement CAPA’s, change controls and site quality and improvement initiatives.
  • To review/approve method validation/verification protocols and all various other miscellaneous studies.
  • To coordinate with cross-functional teams (CFT’s) for any kind of unresolved issues and to resolve,
  • To escalate any kind of unresolved quality/ resource-related issues to the next level.
  • To participate/ facilitate cross-functional teams for investigations and provide oversight on microbiology aspects to the investigation teams.
  • Creating quality/compliance/safety awareness among the team members through periodic team meetings.
  • To keep up to date with changes in the pharmacopoeia/ regulations/guidelines and cascade the same to the -teams for awareness and to organize the creation/revision of the laboratory procedures in line with the changes for compliance.
  • Review and approval of training modules and to guarantee that a robust analyst qualification program is in place and maintained.
  • To monitor/ participate in the media fills and in media fill failure investigations (if applicable).
  • To review and approve SOP, Specification, Validation protocols and Worksheets.
  • To approve or reject the starting materials, packaging materials, intermediate, bulk and finished products.
  • Ensure that a qualification, maintenance and calibration program is in place and adhered to.
  • Ensure that housekeeping and lab facilities are maintained according to current standards.
  • Guarantee that environmental monitoring systems are in place and maintained for all classified areas, utilities (water, pure steam and gasses) and pure steam at the Vizag facility.
  • Ensure waste management of Biological, toxic and hazardous water materials.
  • Ensure approved contract testing labs are used for all analysis activities.
  • Ensure that procedures are maintained for the storage, handling and destruction of microbial culture.
  • #LI- PFE.
See Also
Centre of Biomedical Research Life Science / Biotech Project Recruitment

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