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Walk In Drive at Indore for Pharma and Science candidates in QC, Production at Lupin

Awareness on current Data Integrity requirements & cGMP requirements, Stability studies. Knowledgeable in handling OOS/OOT/Deviations and QMS (CAPA, CCP etc.) / LIMS Software.
Quality Control, Quality Assurance, Production Jobs at Glenmark Pharma
Analysis of Raw material, Stability and Finished product samples, must have hands on experience of instruments like, HPLC, GC, UV, KF, ICPMS & IR etc., QC investigation and QMS.
Apprenticeship in Production, QA, QC, ADL at Bharat Parenterals
Bharat Parenterals Ltd. is a Gujarat based pharmaceutical company, established in 1992 by Mr. Ramesh Desai, who started the company with a vision of making world class affordable medicines.
QA, QC, Packing Jobs at Torrent Pharma
Torrent Pharma, the flagship Company of Torrent Group is one of the leading pharma companies of the Country.
QA, QC, Production, HVAC, Warehouse Jobs at Gufic Biosciences
Knowledge of Injectable plant in IPQA, GLR QMS, Validation, Vendor Qualification, Audit Compliance
National Postdoctoral Fellowship under IITI–ANRF PAIR Theme
Medical postgraduate in relevant disciplines such as Microbiology./ Biotechnology / Biomedical Sciences / Molecular Biology / Life Sciences / Pharmaceutical Sciences/ Medical Technology or allied areas.
NIPGR Advertisement for Life Sciences Professional
Candidates having Masters degree in any subject of Life Sciences with at least one year of research experience in the field of Bioinformatics / Data Science / Machine Learning / AI or related fields are eligible to apply.
Fellowships for Life Sciences, Biochemistry, Biotechnology at Jamia Hamdard
MSc. degree (with minimum 55% marks) in Life Sciences / Molecular Medicine/ Biochemistry / Biotechnology or equivalent subject.
IITI-ANRF National Postdoctoral Fellowship
PhD in Chemistry / Biomass Conversion / Animal Biotechnology / Plant Biotechnology / Molecular Biology.
Regulatory Affairs Jobs at Macleods
Experience in Pharmaceutical Regulatory Affairs, prepare & submit Regulatory documentation to authorities, Compile original ANDA modules submission knowledge of changing FDA requirements for solid oral, injectable, MDI.