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September 2025

Rusan Pharma looking for Area General Manager

Strong knowledge of GMP regulations including WHO, EU GMP, PICS, TGA, MHRA, USFDA & other global regulatory guidlines. Expertise in handling CAPA, CCF, deviations, market complaints, product recalls if any.
BRIC-RGCB Opening for Chemistry, Biochemistry, Biotechnology candidates
Good Academic record with First Class Masters Degree in Chemistry/Biochemistry/Biotechnology with a qualified National Eligibility Test–CSIR-UGC-NET/LS or DBT-BET/ ICMR/Fellowship or GATE
Sun Pharma Hiring Packaging & Device Development Senior Officer - B.Pharm Apply
Preparation & review of New and Existing Products artwork. Responsible to maintained artworks track records in excel.
Interview for Team Member Posts at Dr. Reddy’s | M.Pharm, B.Pharm, MSc Apply
Preparation and Execution of qualification protocols for Equipment's, Autoclave, Tunnel, Filling and capping machine, Lyophilizer, Washing machine, bung processor etc.
Openings for B.Pharm, MSc in Quality Control at Macleods
Macleods is one of the fastest growing pharmaceutical company, having strong presence in various therapeutics segments. Ranked amongst the top 10 companies.
Interview for M.Pharm, B.Pharm, MSc in Quality Control, Production at Aurobindo Pharma
Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India
Amneal Pharma Hiring IPQA Trainee Officer - B.Pharm, M.Pharm Apply
To perform the role & responsibilities defined as per TMS software. Escalation to Superior for major non- conformities timely.
Openings for Research Associates and Team Lead posts at Dr. Reddy’s Biologics
Skilled in medical device packaging and Visual inspection, with expertise in strategic planning, documentation, aligned with cGMP standards.
Openings in Regulatory Affairs at JAMP group
Assist in the preparation of response packages to Health Canada requests in a timely manner to minimize delays in the submission review process. 
Work as Clinical Trial Associate at Novartis
Designs and coordinates the overall direction of clinical development projects. Coordinates activities of associates and investigators to ensure compliance with protocol and overall pre-clinical objectives. Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings