Handling HPLC, UPLC and GC. Knowledge in handling empower 3 software. Experience from Regulatory approved Sites are preferred.

Online filling of the BPRs and records and performing jobs related to SAP, Operate equipment's reactor, Sparkler Filter, Candle Filters , Centrifuge, Dryers as per SOP

To author and review quality agreements between Sun Pharma & CMO site. Also, ensure qualified and approved external service providers are used.

Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates.

Post Graduation Degree in am branch of Life Science, Medical Sciences, Pharmaceutical Sciences, or Biotechnology Plus 2 years of research experience with or without NET, NET, GATE, Equivalent

Assessing Phenytoin and Levetiracetam Efficacy, Cost- Effectiveness and CYP2C9, SV2A Polymorphism in Early Post-Traumatic Seizures, A Multicentric Prospective Randomized Trial; Post graduate Degree including integrated PG degree with PhD Biochemistry, Biotechnology, Microbiology, Pharmacology and other allied subjects

Post graduation in life science OR Masters degree, diploma in life sciences, pharmacy, public health, healthcare or other related discipline with one year of post qualification relevant clinical research experience; Effects of extreme heat on maternal, placental and fetal physiology, lactation and newborn health in India

First Class Post Graduate degree from a recognized University in Biochemistry, Immunology, Molecular biology, Biotechnology, Pharmacology

BE, B.Tech, ME, M.Tech, MS, M.Sc,B. Pharm, M.Pharm, MBBS, BDS or equivalent degree in relevant disciplines, specializations.

A new Chemo-enzymatic process for the synthesis of Pregabalin; M.Sc. in Biological Sciences, Microbiology, Biotechnology , Biochemistry, Life Science, Biochemical Engineering or Technology from a recognized University or equivalent.

Demonstrating a good degree of competence in regulatory affairs and understanding of dossier technical requirements within the region, this role provides technical subject matter expertise to support Country RA teams with their local publishing and agency submission transmission needs.

To create an awareness regarding antibiotic resistance. Postgraduate degree in basic science or graduate/ post graduate degree in professional course

Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy, safety profiles to support on-label prescribing for appropriate patients.

Bachelors, Master degree or PhD in science, math, engineering or related discipline; The Principal, Regulatory Affairs, Intelligence, Materials is expected to perform with minimal supervision and is an experienced and detail-oriented professional with expertise in materials and with an understanding of the interplay of materials and medical devices, pharmaceuticals and combination products.

A Phase-lV, single-arm, multicentric study to assess the safety of SIIPLs qHPV vaccineCERVAVAC when administered in a two-dose schedule to girls and boys aged 9-14 years and in a three dose schedule to women and men aged 15-26

Candidates holding Postgraduate, Master’s degree M.Sc. , M.Tech. , M.Pharm etc. Two Years Course in the area related to life sciences including botany, chemistry, biochemistry, biotechnology, agriculture sciences, microbiology, plant sciences, pharmaceutical chemistry, food technology

M.Pharm, M.Sc, M.Tech Bioinformatics, Pharmaceutical Chemistry or Biotechnology. Experience in Molecular Modelling, Computer-aided drug design, ML, AI skills with experience in various tools

B. Pharm, B.Sc. for BA BE and For clinical B. Pharma or M.Sc. Or M.B.B.S.B. V. Sc. and A.H is compulsory. M. V. Sc. Pharmacology and Toxicology is desirable for preclinical; Check CROs for conducting preclinical/ clinical/ bio equivalence studies by site feasibility/ selection visits or evaluation for ensuring adequate facility, skill and experience for conducting the studies as per requirements

Dossier and document preparation as per CTD,ACTD and country specific guidelines, Review of dossiers, DMF and Technical documents, Answer query raised from regulatory authority, package insert, SmPC, PIL & MSDS preparation