Job in Production, Quality Assurance, Quality Control, Regulatory Affairs at Hetero Biopharma | Walk in

 

 

Hetero Drugs established in the year 1993, with the motto to be the best in the API manufacturing, Hetero today embodies the vision of a top notch player in developing and commercialising products catering to a variety of therapeutic categories, integrating into a leading finished dosage manufacturer. True to the Statement, "Where the Future Started Yesterday", with a foresight on the current trends in the Pharmaceutical Market, Hetero has grown from strength to strength, combining its Research Strengths, Manufacturing Capabilities ,Human Resources and well established quality management system.

PRODUCTION /MANUFACTURING

Officer-Sr.Executive (UPSTREAM PROCESS)
Experience : 02-06 years
Job Profile : Upstream/Cell Culture with good exposure on Bioreactors & Fermenters. Sound knowledge in GMP Documentation.

Officer - Sr.Executive (DOWNSTREAM PROCESS)
Experience : 02-06 years
Job Profile : Downstream/Purification with good exposure on chromatography & Filtrations. Sound knowledge in GMP Documentation.

QUALITY ASSURANCE - IPQA

Officer/Executive/Sr.Executive
Experience : 02-06 years
Job Profile : Responsible for giving line clearance before start of manufacturing activities for Drug substance and Drug product Review of the master and executed batch manufacturing records Review of the Manufacturing and QA SOPs.

QUALITY CONTROL

Officer/Executive/Sr.Executive
Experience : 02-06 years
Job Profile : Review of analytical data. Experience in testing on Biopharma products Handling of UPLC and HPLC. Sound knowledge on Empower3 software & should have QMS exposure.

REGULATORY AFFAIRS

Manager/Sr.Manager
Experience : 09-12 years
Job Profile :
Preparation of CTD dossier (Module 1, 2, 3,4, 5 and Administrative / Statutory documents) for registration in Global markets for Biopharma products. Expertise in obtaining all regulatory licenses, certificates. Good exposure in Analytical, Manufacturing & Quality background shall be given a preference.
Clinical trial design, operations & CSR preparations for global markets. Clinical (module 5) content development & Medical writing. Relevant experience in Clinical CRO's, Pharma/Biopharma companies is essential and experience in medico-regulatory is preferred.

Documents to be carried:
One passport photo, 3 months payslips & recent increment letter/appointment letter with annexure copy

Date : 09th Mar 19(Saturday),
Timings: 9.00 AM to 3.00 PM
Venue : Hetero Corporate Office
# 7-2-A2, Industrial Estates, Sanath Nagar, Hyderabad, Telangana
Landmark: Opp to Police Station

Candidates those who cannot attend this drive can share their resume to vinaykumar.b@heterodrugs.com / raghava.n@heterodrugs.com

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