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  • Multiple Job openings for M.Pharm, M.Sc in Etico Lifesciences Private Limited

    Etico is an ethical pharmaceutical company founded in 2016 and based out in Hyderabad, India. We are specialized in development of oncological and non-oncological parenteral dosage forms development and provide product development and technology transfer solutions to innovator and generic pharmaceutical companies worldwide.

  • Job for Senior Executive in R&D (API) at Ind-Swift

    Established in 1995 Ind-Swift has fast evolved towards a business model that is focused on deep-rooted domestic presence and leveraged on high-value mature regulated markets along with considerable growth in emerging markets.  With manufacturing sites at 6 different locations across India and an independent State-of-the-Art R&D Centre, the Group has embarked upon a journey to establish itself as reliable partner in the Global Pharmaceutical Industry. In house capabilities for Development of APIs, Finished Dosage forms, Non-Infringing Process & World Class facilities for Contract Manufacturing are the inherent strengths.

    Post : Sr. Executive / AM – ARD || R&D (API)

  • Job for M.Pharm, M.Sc in Manufacturing, Packaging at SANOFI | walk in

    SANOFI is a global healthcare company committed to improving access to healthcare and supporting the people we serve throughout their health journey.

    Post : EXECUTIVE / ASSISTANT MANAGER PHARMA MANUFACTURING / PACKAGING

  • Job for Senior Officer in Production at Mankind Pharma

    Mankind Pharma, one of the top 5 leading pharmaceutical companies in India, started its journey in 1995. Today, we have 12,000 employees and are heading towards a turnover of INR 50000 million.  Our vast network includes 61 C&F agents and 6000 stockists. We provide a wide range of products – Antibiotic, Antifungal, NSAIDs, Gastrointestinal, Anthelmintic, Cardiovascular, Dermal, Erectile Dysfunction, and several other categories – across the nation.

  • Job for M.Pharm, M.Sc as Research Associate at Aurigene

    Aurigene is a specialized biotech company, focused on oncology and inflammatory diseases. Aurigene has deep target and therapeutic area expertise, gained from the experience of multiple programs reaching global clinical development from its efforts. Aurigene has pioneered a unique, collaborative business model to work with pharma and biotech partners, in a win-win partnership that combines Aurigene’s deep expertise in oncology and inflammation, with our collaboration partners’ needs for expertise, scalability and high-quality, quick and cost-effective prosecution of targets.

    Post : Research Associate – CMB

  • Vacancy for Junior Regulatory Affairs Associate at PAREXEL

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

    Post : Junior Regulatory Affairs Associate

  • Work as Scientist in Bioanalytical at USP

    The United States Pharmacopeia (USP) is a non–governmental, official public standards–setting authority for prescription and over–the–counter medicines and other healthcare products manufactured or sold in the United States. USP also sets widely recognized standards for food ingredients and dietary supplements. USP sets standards for the quality, purity, strength, and consistency of these products–critical to the public health. USP's standards are recognized and used in more than 130 countries around the globe. These standards have helped to ensure public health throughout the world for close to 200 years.

    Post : Scientist II, Bioanalytical

  • Job for Analytical Scientist at Syngene International Limited

    Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

    Post : Research Associate/ Senior Research Associate/Associate Scientist/ Sr. Associate Scientist

  • Walk in Interview for M.Pharm, B.Pharm, M.Sc in Quality Control at Ajanta Pharma Limited

    Ajanta Pharma Limited is a specialty pharmaceutical company engaged in development, manufacture and marketing of quality finished dosages in domestic and international markets. We are looking suitable candidates for below openings at our flagship formulation facility located at Paithan Aurangabad, which is approved by the US FDA, UK MHRA. It also holds WHO pre- qualification.

    Post : QC Sr. executive/Executive/Sr. Officer / Officer

  • Job for M.Sc in Production at Syngene International

    Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

    Post : Jr.Exe/ Asso.Exe/Exe/Sr.Exe/Jr.Mgr-Production(API)

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