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Walk in interview in Production, Regulatory Affairs, Product Development at Apotex Research

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Apollo Pharmacy hiring

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Apotex Research Pvt. Ltd. is a wholly owned subsidiary of Apotex Inc. Canada which is a number one generic pharma co. in Canada. The position is for Bangalore location which has an R&D Centre, Manufacturing and a Bioequivalence Centre.

Post: Manager, Pharmacist, Team Leader, Technicians, Research Scientist


Analytical Operations ( Research Scientist / Sr. Research Scientist ): M. Pharm/M.Sc. with 3-9 years of experience, with exposure to product development activities for regulated markets, exposure to solids orals / semi solids will be added advantage. 

Formulation Development ( Research Scientist / Sr. Research Scientist ) : M. PHARMA with 2-5 years of experience in solid oral dosage form development for regulated market. Exposure to USFDA, MHRA, Health Canada, TGA Markets. Quality by Design and Planning of experiments using DoE is desirable.  Technical Operations

Technical Operations ( Research Scientist / Sr. Research Scientist ) :  M. PHARMA with 2-5 years of experience in scale-up and technology transfer of solid oral dosage form for regulated market. 

Product Evaluation & Analytical Support: M. Pharma / M. Sc. in chemistry with 2-6 years of experience in stability studies / stability data trending ( preferably in NWA software / stability documentation) for regulated markets.


Production ( Production Technician / Operator / Machine Operator ):  Diploma in engineering /  Pharmacy /  B.Sc. with 2-7 years of experience in manufacturing/packaging of tablets and capsules. Hands on experience in granulation, compression, coating, blister packaging, cartonator, or bottle packing. 

Production ( Pharmacist / Officer / Executive / Team Leader ):  B. Pharma/M. Pharma with 2-8 ( Pharmacist / Sr. Pharmacist ) 0r 10-14 years (Team Leader) of experience in manufacturing and packaging of tablets and capsules.

Regulatory Affairs ( Associate / Sr. Associate ): M. Pharma with 3-5 years of experience in dossier compilation & submission of US, Canada or EU markets. Experience in submission and post approval management. 

Regulatory Affairs ( Group Leader / Dy Manager ) : M. Pharma 8-12 years of eCTD publishing experience. Experience in regulated markets for solid oral dosage form is a must. 

Regulatory Affairs ( Sr. Associate / Team Leader ) : 5-10 years of experience in Regulatory compliance/plant regulatory affairs. Experience in post approval life cycle management or regulatory compliance is a must. 

Regulatory Affairs Labelling ( Group Leader / Dy Manager) : B. Pharma with 8-10 years of experience in labelling for new submissions and product lifecycle management for US & Canada markets. Exposure to other regulated markets and eCTD will be an added advantage.

Additional Information:
Experience : 2-10 years
Qualification : B.Pharm, M.Sc, M.Pharm
Location : Bangalore
Industry Type :  Pharma / Biotech / Clinical Research
Functional Area :
Production, Manufacturing, Maintenance

Walk in Interview
23rd Saturday & 24th Sunday July 2016. 
Time: 9.00 AM to 4.00 PM

Sri Venkateshwara College Of Pharmacy,86, Hitech City Road, Madhapur, Hyderabad, Telangana 500081

Candidates are requested to carry 2 copies of resume, passport photo, pay slips, Education certificates, salary annexure and previous experience certificates.

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