D.Pharm, Integrated Pharmacy Course for certificates issued by Government. vacant posts on a lump sum basis through the District Welfare Association on the basis of contract of the Siddha Medical Department.

To support the teaching needs of the M.Sc. in Clinical Research program with a specialization in Clinical Trials at THSTI.  Contribute ongoing and future clinical trials, epidemiological studies, and other health- related research projects by providing robust statistical expertise.

A Diploma in Pharmacy, Bachelor of Pharmacy. Must have registered with Pharmacy Council and must keep the registration alive by renewing it regularly every year.

BPharm, BSc, MPharm, MSc, MBBS, BAMS; Experience in PV/ Clinical Research drug safety preferred. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.

TCS combines tech expertise and business intelligence to catalyze change and deliver results. Our mission is to help customers achieve their business objectives by providing innovative, best-in-class consulting, IT solutions and services and to make it a joy for all stakeholders to work with us. Clinical Data, Regulatory, Clinical Operations, Pharmacovigilance; Should be open to work In shifts

Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines

As part of our team, you'll be responsible for a diverse range of tasks within the drug discovery process. In this role, you will have ample opportunities to collaborate with our dynamic team, providing scientific expertise and strategic leadership.

Hands-on experience with HPLC, GC, UV-Visible Spectroscopy and Dissolution tester. Proficient in Empower-3 software. Strong analytical and problem- solving skills.

As Technical Leader, define, organize, plan and lead the projects that are technically complex and cross functional in nature at a global front. Broad understanding of the overall product and therapy along with deep technical expertise in one or more fields related to drugs and medical devices

The Clinical Data Management Associate is responsible for providing expert skills as part of the clinical data management team within the Data Management and Statistics Department to ensure that efficient and quality data management products are produced in accordance with customer requirements.

The Senior Specialist, Expert License Management prepare dossiers and execute actions that support the license security and product compliance on the markets, and that meet companys and health authorities requirements. Encounter the challenges to enable representatives from all major disciplines involved to reach agreement on the license management strategy and approach.

Ph.D, MD, MS, MDS or equivalent degree or having 3 years of research experience after MVSc, M.Pharm, ME, M.Tech with at least one research paper in Science Citation Indexed journal.

To work in Clinical Trials as a Non-Medical Co-ordinator. Pharmacist for the Department of Endocrinology, Diabetes & Metabolism. B.Pharm, with Tamil Nadu Pharmacy Council Number.

Prior experience in virology or immunology is desirable. Candidates must have experience in immunological or virological assays for BSL2 or BSL3 labs. Animal handling and experimentation is desirable. 

Ph.D or Ph.D thesis submitted or defended experience Biochemistry, Biotechnology, Stem Cell Biology and Neurobiology, Neuroscience with a strong publication record and research experience in Cell Biology, Molecular Biology and Neurobiology.

Expertise in different types of purification techniques. Sound knowledge of different column chemistry used in HPLC. Responsible for troubleshooting of instruments and their calibration

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Ensure that Bulk Viral Antigen production adheres to GMP standards on the shop floor, including line clearance, dispensing, and preparation processes. Examining and approving batch records, standard operating procedures, project plans, customer verification, and APS documents.

Post Graduation in Science M.Pharm, Life Sciences, Biotech, Zoology, Botany, etc. With PG Diploma in Clinical Research is mandatory. Candidates should have at least one-year experience as Clinical Trial / Research Coordinator is mandatory.