Skip to main content

Ipca Laboratories Limited Invites Pharma candidates in Production, QA, Stores

For more than 60 years. Ipca has been a crucial healthcare partner in over 120 countries across the 6 continents. We are a fully-integrated pharmaceutical company that manufactures over 350formulations and 80 APIs for various therapeutic segments. Today, we are one of the world’s largest manufacturers and suppliers of over a dozen APIs. These are produced from scratch at fully-automated manufacturing facilities, approved by the world's most discerning drug regulatory authorities like UK-MHRA. EDQM-Europe. and WHO Geneva, among others.

Interview for Drug Safety Associates at Indegene
Interview for Drug Safety Associates at Indegene

Indegene help biopharmaceutical, emerging biotech and medical device companies develop products, get them to the market, and grow their impact through the life cycle in a more effective, efficient, and modern way. We bring together healthcare domain expertise, fit-for-purpose technology, and an agile operating model to provide a diverse range of solutions. These aim to deliver, amongst other outcomes, a personalized, scalable and omnichannel experience for patients and physicians. It’s what drives our team and our purpose to enable healthcare organizations to be future ready. 

Require Regulatory Compliance Senior Manager at EY
Require Regulatory Compliance Senior Manager at EY
As a Senior Manager – Regulatory Compliance, you will lead IT implementation projects in regulated GxP environments, leveraging your deep expertise in Regulatory Affairs and Regulatory Information Management Systems (RIMS) and strong consulting capabilities.
Work as Clinical Evaluation Manager at Zydus Lifesciences
Work as Clinical Evaluation Manager at Zydus Lifesciences
Bachelors or masters degree in Life Sciences (e.g., Biomedical Engineering, Nursing, Medicine, Pharmacy). Zydus Lifesciences
Apply Online for PK Medical Writer at ICON plc
Apply Online for PK Medical Writer at ICON plc
Advanced degree in Life Sciences, Pharmacy, Medicine, or related field, with a minimum of 3-5 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization industry.
Work as Associate Senior Clinical Data Scientist at Novo Nordisk
Work as Associate Senior Clinical Data Scientist at Novo Nordisk
Bachelors or Masters degree in life sciences, natural sciences, engineering, or equivalent qualifications. 2-3 years of programming experience, preferably working with biological data or equivalent knowledge through relevant practical experience. 
IQVIA Require Clinical Data Specialist
IQVIA Require Clinical Data Specialist
Bachelors Degree Clinical, biological. Provide basic and some comprehensive data management expertise to the Clinical Data Management, CDM team to provide efficient, quality data management products that meet customer needs. IQVIA
Clinisys looking for Senior Regulatory Analyst
Clinisys looking for Senior Regulatory Analyst
Bachelors degree in Regulatory Affairs, Science, Life Sciences, Healthcare. Author and maintain regulatory documentation including technical documentation, declarations, regulatory assessments, intended use statements, labeling reviews, and compliance records.
Production, Microbiology, Packing Openings at Acme Generics
Production, Microbiology, Packing Openings at Acme Generics
The Acme Group began its journey in 2005 with a bold mission of becoming a leader in the contract manufacturing space and a preferred business partner for pharmaceutical companies seeking world-class capabilities and scalable operations.
Technical positions for Pharma, Chemistry, Life Sciences candidates at NIT Agartala
Technical positions for Pharma, Chemistry, Life Sciences candidates at NIT Agartala
Four years Graduate degree in Biotechnology, Biochemical Engineering, Bioengineering, Biotechnology & Biochemical Engineering, Chemical Engineering, Biosciences and Bioengineering, Food Engineering/Technology, Pharmacy and allied disciplines. NIT Agartala