M.Sc. in Medical Microbiology / Biochemistry / Biotechnology / Public Health / Physician Assistant or Pharm.D. Kasturba Medical College, Manipal.

Masters degree in Microbiology, Biochemistry, Biotechnology, Microbial Biotechnology, Industrial Biotechnology, Pharmaceutical (Bio)Technology, Biochemical Engineering, or equivalent degrees in relevant fields from a recognized University / Institute, NCL Pune

M.Sc. (Biotechnology/Microbiology/Biochemistry or relevant life sciences discipline) with a minimum of 55% marks. funded by Gujarat State Biotechnology Mission, Govt. of Gujarat at Gujarat Biotechnology University (GBU)

MSc (Bioinformatics / Biophysics / Biochemistry / Biotechnology) or Masters degree in any other stream of Biological / Physical /Computational Sciences, NII Pune

M.Sc. (Life Sciences/Biotechnology) or M.Tech. Biotechnology Qualified GATE Experience with protein NMR is preferred. Indian Institute of Technology - Roorkee 

M.Sc in Life Sciences from a recognized university/institution with 2 years of Research Experience. Dr. R.P. Centre for Ophthalmic Sciences, AIIMS.

MSc. in Virology / Microbiology / Biotechnology from a recognized University/Institution, with two or more years of research experience. 

Sun Pharma is inviting passionate professionals to join Indias No. 1 pharmaceutical company and contribute to delivering medicines worldwide.

Conduct in-process and retrospective audits for studies and method validations. Review reports, source data, audit trails and regulatory compliance. 

Ciron has carved a niche for itself in the sphere of operations of manufacturing Ampoules, Vials, Eye / Ear / Nasal drops, Lyophilized products and Lyophilized bulk. Manufactured in India

Serves as a Clinical Data Reviewer and identify any errors in data by performing data review per DRP and issuing/closing queries.

Responsible for providing this service to clients either as a support function to the client project groups or as stand- alone business.

Provides support according to the needs for delivery activities, i.e. co-authoring safety documents and assisting in providing safety input to regulatory and clinical documents, as well as ad hoc Health Authority queries.

Responsible for preparing lower complexity documents such as synoptic or abbreviated CSRs under guidance of more senior staff. Assist Medical Writers in the preparation and background writing of clinical study protocols, CSRs, and subject narratives.

Senior Principal Consultant - Validation leads enterprise‑level validation strategy by shaping frameworks, harmonizing standards across portfolios, and ensuring global regulatory compliance while driving high‑risk programs, organizational capability building, and long‑term CSV transformation with executive stakeholders.

Contributes, with appropriate oversight, to all relevant aspects of global clinical trial activities to deliver study outcomes within schedule, budget, quality, compliance and performance standards. May lead specific aspects of global clinical trial. High quality contributions to study documents e.g. protocol, ICF, clinical sections of CTA -Clearly demonstrates Novartis Values and Behaviors i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity.

Coordinates data cleaning tasks and delegates to appropriate data management staff to ensure quality standards are maintained and project deliverable timelines are met with minimal supervision.

Performs E2E process related scientific writing that includes but not limited to manage workflow in PubConnect, create publication plan, author approvals, pre-submission queries, submission activities etc.

Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.