Apotex is a Canadian-based global health company. We improve everyday access to affordable, cutting-edge 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.
Preparation of various master documents required for the submission batch execution and supports the product development by preparation of documents like master production records, Master Packing records and various reports like Exhibit Batch Summary Reports, Hold Study reports, Photo stability Reports, Transportation worthiness study report, Bulk product Stability Reports, SOP's and other miscellaneous reports.
Responsible for Maintenance & updating of proper inventory of all the change parts and accessories for the equipments and Instruments.
Indenting the punches, dies & machine change parts for the development and submission batches. Preparation of Purchase indents in SAP for the procurement of raw and packing materials.
Perform all work in accordance with established regulatory, compliance and safety requirements.
Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
for the Formulation Development Laboratory.
To maintain the safety and housekeeping practices at workplace.




To maintain online documents for the activities carried out by him/her in the area.
Produce quality products by following GMP practices and maintaining the yields / reducing the packaging materials waste.
To receive, check, issue and dispense raw materials and packaging materials.
To be responsible for all activities in the Day Stores and Pilot plant including cGMP, documentation and implementation of departmental quality systems.
To generate and maintain records involving the receipt, checking, issue and dispensing of raw materials and packaging materials.
University / College degree in Chemistry, Pharmaceutical Technology, or related science preferable B. Pharm/ M Pharm (Pharmaceutics)
Should have good communication knowledge of English (Speaking, Reading and Writing).
Should have skills in Microsoft Word, Excel and working knowledge in SAP. Knowledge of the Pharmaceutical manufacturing Process and cGMP is desirable.
Should have the attitude of performing the allotted activities in compliance with all the established procedure with an aim to develop Quality Pharmaceuticals.
Should take ownership for quality in the job, support our corporate values of Collaboration, Courage, Perseverance, and Passion.
Experience
Should have minimum 5 year's experience in Technical Writing in the pharmaceutical industry/ GMP environment and overall 6-8 years working knowledge of Formulation Development, Manufacturing process in pharmaceutical industry.

We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

📌 Development Director / Head of Production (Bengaluru)
🏢 Apotex Research
📍 Bengaluru