Associate Quality Assurance

4 - 6 years

1 - 4 Lacs

Posted:1 day ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Part Time

Job Description

Preferred Education/ Qualification B. Pharm/M. Pharm/M.Sc.
Experience: 4– 6 years of experience in Quality Assurance / MQA of sterile dosage manufacturing facility.
Core Competencies :
  • Technology Transfer
  • Change Management process
  • Risk assessments principles and tools
  • Validation of manufacturing equipment’s
  • Drug Product Process validations
  • Regulatory requirements Compendial Changes
Technical Skills
  • Fundamental knowledge on manufacturing and Quality control activities, such as Solution preparation, filling, terminal sterilization, visual inspection, packing, in process sampling and analysis.
  • Technical document review skills
  • Knowledge in change control assessment
  • Knowledge on manufacturing process such as stopper processing, sampling and dispensing, solution preparation, Component Preparation, Filling and Capping of Drug Product
Behavioral/Any Other Skills
  • Acts Decisively: Makes decision in a timely manner based on available information
  • Grows Self: Identify Individual development needs and create a plan and work towards achieving those objectives
  • Critical thinking and Compliance mindset
Core Responsibilities
  • Good performance, partially independent, reviews trends and data
  • Responsible for review of Manufacturing documents such as SOPs, Process validation, cleaning validation, cleaning process verification documents, Batch manufacturing records, Exhibit batch plan, Exhibit batch Summary Reports. study protocols and reports.
  • Tracking of change controls, Providing QA Impact Assessment, preapproval, post approval & closure of action items.
  • Coordinating with CFT for addressing & resolving of Review Comments for timely Closure.
  • Review of product & process related SOP, Job aids & Forms.
  • Review and approval of NVPC, PH and conductivity.
  • Review and approval of APQR’s.
  • Report any non-compliance to the Supervisor

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control
#LI-PFE

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Pfizer

Pharmaceutical Manufacturing

New York New York

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