Quality Assurance Job at Apotex | Pharmacy Graduates Apply Now for the Executive Role
Join Apotex, a leading Canadian-based global pharmaceutical company, as an Executive – Quality Assurance Operations in Bangalore. This Quality Assurance Job offers an exciting opportunity to ensure compliance, product quality, and operational excellence in a GMP-regulated manufacturing environment. If you are passionate about maintaining high-quality standards in pharmaceutical production and want to grow in a global, innovation-driven company — this is the perfect opportunity for you.
- Job Post: Executive, Quality Assurance Operations
- Location: Bangalore, KA, IN, 560099
About Apotex Inc.
Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico, and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.
Pharmacy Job Summary
- IPQA activities.
- Warehouse QA activities
- MMaR’s / MPaR’s Review.
Pharmacy Job Responsibilities
- Line clearance of Various in process stage such as Dispensing, Granulation, Compression, Coating, Packaging, and Sampling.
- Routine monitoring of all functional area to ensure adherence to the SOPs.
- Co-ordination & Ensuring timely execution of Sampling activity of Raw and Packing materials.
- Co-ordination of daily activities in Manufacturing and packaging areas.
- Create signature and methods for raw materials by using Truscan RM analyzer.
- Approved / Rejected labels affixing for API, Excipients, Primary packing, and secondary packing materials finished goods and operation supplies.
- Verification of Temperature and Relative Humidity reports generated from TESTO software.
- Co-ordination & ensuring timely execution of in-process activities for manufacturing and Packaging.
- Coordination for implementation of CAPA.
- In-process checks during manufacturing & packaging stage, Performance of AQL, collection of samples as applicable and trending of AQL.
- Sampling of validation & commercial batch, Shelf life expiration date (SLED), Bulk completion date (BCD), sampling, Hold time study sample, In-process samples/Finished product samples, Collection, storage, and disposal of Reserve Sample.
- Preparation, Review and updating of standard operating procedure.
- Planning, co-ordination, and sampling of Raw and Packaging materials.
- Co-ordination for Process validation & cleaning validation execution.
- Approved/ Rejected labels affixing for API, Excipients, Primary and Secondary packaging materials.
- Swab/Rinse sampling for the cleaning verification & validation program, cleaning & verification of sampling thief’s & accessories.
- Co-ordination for in-house and external calibration.
- Review of Master Manufacturing Records & Master Packing records & logbooks.
- Works as a member of a team to achieve all outcomes.
- Performs all work in accordance with all established regulatory and compliance and safety requirements.
- Preparation for regulatory audits and making the compliance for the same.
- To ensure that the impact of any risk reduction measures is not detrimental to the systems, facilities, utilities, equipment, or processes.
Job Requirements
Education
Bachelor of Pharmacy/ Science or any equivalent degree.
Knowledge, Skills and Abilities
- Should possess good communication and interpersonal skills along with Computer efficacy in MS-Office and Internet.
Experience
Minimum 02 Years of experience in GMP Regulated Pharmaceutical industry.
