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Trainee, Quality Assurance

0-1 years
Not Disclosed
10 Oct. 31, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Trainee, Quality Assurance

📍 Location: Bangalore, Karnataka, India (560099)
📅 Date Posted: October 29, 2025
🏢 Company: Apotex Inc.


About Apotex Inc.

Apotex is a Canadian-based global health company dedicated to improving everyday access to affordable and innovative medicines for millions worldwide.
With a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals, and consumer health products, Apotex stands as Canada’s largest pharmaceutical company.

Headquartered in Toronto, with regional offices across the United States, Mexico, and India, Apotex serves as a trusted health partner for pharmaceutical licensing and product acquisitions.

🌐 Learn more: www.apotex.com


Job Summary

As a Trainee in Quality Assurance (QA), you will support the execution of QA-related activities within the manufacturing and packaging units.
Your responsibilities include sample collection, documentation, review, and support to IPQA operations, ensuring compliance with regulatory and safety standards.


Key Responsibilities

  • Support sampling activities for:

    • Raw materials and packing materials

    • Blend uniformity and swab/rinse samples

    • Hold time study, SFG (Semi-Finished Goods), and FG (Finished Goods) stage samples

  • Collect and submit stratified and pooled samples to the Quality Control (QC) department.

  • Submit executed batch documents to the release team and document cell.

  • Arrange and maintain sampling accessories, reserve samples, and hold-time sample cabinets.

  • Clean sampling aids, accessories, and IPQA cabinets.

  • Perform destruction of reserve samples as per procedures.

  • Manage the request, receipt, and submission of protocols and logbooks to the document cell.

  • Handle issuance of Apo Web formats and other related documentation.

  • Organize IPQA area cupboards within manufacturing and packing areas.

  • Review executed logbooks of manufacturing and packing areas.

  • Provide support to IPQA personnel for various in-process and compliance activities.

  • Maintain compliance with all regulatory, quality, and safety requirements.

  • Work collaboratively as part of a team, demonstrating Apotex’s values:
    Collaboration, Courage, Perseverance, and Passion.


Education

🎓 Required: B.Sc. / B.Pharm / Science or an equivalent degree.


Experience

🧪 Required: 0–1 year of relevant experience in pharmaceutical quality assurance or a related field.


Knowledge, Skills, and Abilities

  • Strong communication and interpersonal skills.

  • Positive attitude and professional temperament.

  • Proficiency in MS Office (Word, Excel, PowerPoint).

  • Attention to detail, documentation accuracy, and organizational ability.

  • Basic understanding of QA and GMP (Good Manufacturing Practices) principles.


Core Competencies

  • Teamwork and collaboration

  • Quality focus and compliance mindset

  • Time management and accountability

  • Process adherence and documentation discipline


Work Environment & Inclusion

Apotex is committed to providing a welcoming, inclusive, and accessible work environment where everyone feels valued, respected, and supported.
Applicants requiring accommodations during recruitment or interviews are encouraged to inform us in advance.


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