The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global Lifescience company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives. The group aspires to become a global life-sciences company transforming lives through pathbreaking discoveries. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil.
Department: Production (API)
- Designation: Officer | Executive
- Qualification: BSc | MSc (Chemistry)
- Location : Dabhasa
- Experience: 2 – 5 years relevant experience in API regulated plant
Candidates should have an adequate exposure in handling reactors, centrifuges and clean room equipment with sound knowledge in cGMP and SOPs. Should have exposure to regulatory requirement of documentation and also adherence to Quality, Safety, Health and Environment measures.
Department: Quality Control (API)
- Designation: Executive | Senior Executive
- Qualification: B.Sc | M.Sc (Chemistry)
- Location : Dabhasa
- Experience: 2 – 5 years relevant experience in API regulated plant.
Should have relevant exposure in analyse the Raw materials, In-process & intermediates finished product and stability samples as per respective test procedures. Expertise in handling HPLC, GC, UV, IR, KF, Melting point etc. To perform the daily calibration of Instruments / Equipment. Preparation of STP / SPC / SOP for QC documentation on a routine basis. Hands on Analytical techniques like weighing, pipetting and dilutions with trouble shooting knowledge of various instrument used in QC Lab.
Department: Development QA (API)
- Designation: Executive | Senior Executive
- Qualification: MSc (Chemistry)
- Location : Dabhasa
- Experience: 2 – 4 years
Responsible for document and data control of DQA i.e. Receiving, Distribution, Archival, Retrieval, Control, Storage and destruction. Responsible for sample management activity. Issuance, Logging, Closing and Handling of Incidence and change control DQA/R&D-synthesis/R&D-Analytical. To support in preparation, implementation and compliance of DQA/R&D-synthesis/R&D-Analytical relevant SOPs. Prepare the Specification and Standard testing procedure of API site through change control system (Track wise).
