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PHARMA JOBS POST > Visakhapatnam > Pfizer- Quality Control (QC) Analyst (Walk – In – Interviews) on 28th April 2024
VisakhapatnamWalk In DriveWalk In Interview

Pfizer- Quality Control (QC) Analyst (Walk – In – Interviews) on 28th April 2024

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Last updated: April 20, 2024 9:34 am
ADMIN 1 year ago 2.7k Views
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Pfizer- Quality Control (QC) Analyst (Walk – In – Interviews) on 28th April 2024

Pfizer Healthcare India Private Limited

Job Title: QC Analyst roles.

Walk in interview on Sunday, 28th April 2024 at 8:00 AM

Interview Venue: GINGER HOTEL – GAJUWAKA- VIZAG

#27-8-308/1/1 |Sri Ram Nagar|Srinagar|Near Vadlapudi Railway Gate|Vadlapudi|Gajuwaka |Visakhapatnam 530046.

Job description:

  • Equipment handling experience:
  • Waters HPLC with EMPOWER, GC, IC, UV, IR, Potentiometer, KF, LBPC
  • Preferably: Experience on Analytical method validations, method transfers handling of Stability testing for injectable products.
  • Ensure training records are updated and correctly filed to reflect current testing capabilities.
  • Perform sampling and labeling of materials as per defined procedure and verification of all the equipment / instruments.
  • Interpret and evaluate data in terms of accuracy, precision, trends and potential Good Manufacturing Practices {also cGMP} impact and recommend appropriate corrective actions.
  • Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance to existing policies.
  • Review and revise Standard Operating Procedures (SOPs), analytical methods and related procedures/documents, to keep them current.
  • Perform analyses on finished products, raw materials, and components including entry, review, and/or approval of data in a computerized database and generate EMS reports.
  • Conduct Microbiological protocols on an as needed basis.
  • 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.

Qualifications

Must-Have

  • Bachelor’s Degree/ master’s degree
  • 1 to 5 Years of 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

Nice-to-Have

  • Laboratory work experience with analytical HPLC (High Pressure Liquid Chromotography) technique
  • Experience leading continuous improvement projects
  • Knowledge of lean manufacturing, six sigma methodologies, and statistics
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