Apotex Trainee Job For Pharma Candidates – Apply Online
Trainee – Quality – APQR
Date: Oct 21, 2024
Location: Mumbai, MH, IN, 400079
Company: Apotex
About Apotex Inc.:
Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the
Apotex group is focused on the development and sale of generic, biosimilar, and specialty products.
For more information visit: www.apotex.com.
Job Summary:
- Compile annual product quality reviews (APQRs) per applicable SOPs.
- Collect, analyze, and summarize product review data correctly and completely in a timely manner.
Job Responsibilities:
- Perform Annual Product Quality Reviews (APQRs) compilation as per SOP, which includes:
- Manufacturing Process Overview
- Batches Released / Rejected
- APIs, Excipients
- Changes
- Test Method and Specification
- Manufacturing / Process Validation, Equipment and Utilities Qualification
- Sterility Validation / Qualification (If applicable)
- Packaging Component Deviations/Changes
- Compendial Review
- Deviations
- Critical In-Process Attributes
- Analytical Test Results
- Recalls and Field Alerts, Returns
- Retention Samples Review
- Technical Agreements (as appropriate)
- Marketing Authorizations Variations and Post Market Commitments (as appropriate)
- Complaints
- Stability
- Conclusion and Product Rating
- Concerns, Recommendations, and Issues for Follow-Up
- Perform complete and correct transactions of the data as per SOP/WI’s.
- Summarize and trend analytical data from LIMS or other acceptable systems.
- Ensure that the complete APQR is submitted for review and accepted by the Reviewer and Project Leader QA Product Review/Manager, QA Product Review.
- Coordinate with Project Leader(s) – QA Product Review / Manager for project completion.
- Compile the APQRs within required timelines to ensure adequate time for approvals.
- Respond to Project Leader’s queries for APQR summary reports as required.
- Assist in the preparation, review, and revision of Standard Operating Procedures (SOPs) as required.
- Ensure compliance with GMP, SOPs, regulatory requirements, and established safety standards.
- Work independently and as part of intra/inter-departmental teams to ensure timely completion of tasks.
- Collaborate as a team member to achieve outcomes in a safe manner.
- Demonstrate behaviors that reflect the organizational values: Collaboration, Courage, Perseverance, and Passion.
- Ensure personal adherence to all compliance programs, including Global Business Ethics, Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- Perform other relevant duties as assigned.
Job Requirements:
Education:
- B.Pharm / M.Sc. / M. Pharm
Knowledge, Skills, and Abilities:
- Excellent technical writing, communication, and interpersonal skills.
- Good academic record from 10th class onwards.
- Demonstrated cGMP knowledge.
- Ability to maintain tracking systems for the compilation and review of assigned APQRs.
- Commitment to Corporate Values: Courage, Collaboration, Pride, and Perseverance.
- Ability to work both independently and as part of teams to meet business and quality standards.
Experience:
- Minimum 1-2 years in the pharmaceutical industry with an emphasis on Quality Assurance.
Link to Original Notification to apply: Apply Here
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