QA Job at Apotex | B Pharma Graduates Apply
Apotex Inc., a global leader in pharmaceuticals, is hiring for the Executive, Quality Assurance (B Pharma Job) position in Bangalore, India. For those interested in a QA Job, this is an excellent opportunity for professionals with experience in GMP-regulated environments to join a team committed to quality, innovation, and patient well-being. As a part of Apotex, you’ll contribute to ensuring top-notch standards in manufacturing, packaging, and compliance within a world-class pharmaceutical company.
Job Details
- Job Position: Executive, Quality Assurance
- Location: Bangalore, KA, IN – 560099
About the Company:
Apotex Inc. is a Canadian-based global health company dedicated to improving access to affordable and innovative medicines worldwide. Headquartered in Toronto, Apotex operates in over 45 countries, including key markets in the United States, Mexico, and India. With a strong focus on generic, biosimilar, and branded pharmaceuticals, Apotex is the largest Canadian-owned pharmaceutical company and a trusted global health partner.
Job Description
The Executive, Quality Assurance will be responsible for ensuring compliance with Good Manufacturing Practices (GMP) across manufacturing, packaging, and warehouse operations. You will excel in this QA Job by overseeing in-process quality assurance (IPQA), reviewing manufacturing records, coordinating sampling activities, and actively participating in regulatory audits.
Key Responsibilities
- Conduct line clearance at various in-process stages such as Dispensing, Granulation, Compression, Coating, Packaging, and Sampling.
- Monitor functional areas to ensure adherence to SOPs and quality standards.
- Coordinate and execute sampling activities for raw and packaging materials.
- Support daily activities in manufacturing and packaging areas.
- Review Master Manufacturing and Packing Records (MMaR’s / MPaR’s).
- Perform AQL checks, trending, and sampling for validation, commercial batches, and hold-time studies.
- Coordinate CAPA implementation and process validation activities.
- Review temperature and humidity reports using TESTO software.
- Prepare and review Standard Operating Procedures (SOPs).
- Oversee swab/rinse sampling for cleaning verification and validation.
- Coordinate calibration activities (in-house and external).
- Prepare for and support regulatory audits and ensure compliance.
- Promote a culture of trust, collaboration, and professional development among team members.
Educational Qualification
Bachelor’s degree in Pharmacy or Science (or an equivalent qualification).
Experience and Skills
- Minimum of 2 years in a GMP-regulated pharmaceutical industry. Prior experience in a QA Job will be beneficial.
- Strong communication and interpersonal abilities.
- Proficiency in MS Office and Internet applications.
- In-depth understanding of quality assurance processes, documentation, and regulatory standards.
