Bachelors degree in Pharma/ Science; Territory Sales Executive -Dry Eye and Ocular Health. To achieve target sales of in-line products

Ensure documentation, compliance, and regulatory readiness in various section like IPQA, QMS, Qualification related activities. Design, develop, and optimize new drug formulations of OSD, Ointment and Injectable.

Making a positive impact on the well-being of human life has inspired every aspect of our work. Each day, we at VIMTA touch millions of lives across the globe with the same intent.

MPharm or MSc; Doctorate degree in Life sciences, Biological Sciences/Biochemistry from a recognized University or equivalent

M.Pharma/ equivalent degree in any branch of Life Sciences; Investigating and translating genomic evidence for public health response to SARS- CoV-2

MBBS or PhD or Masters in Biostatistics or Statistics or Epidemiology or Public Health or Clinical Research or Pharmacology or equivalent. 

Deciphering the role of Fibroblast Growth Factors Dynamics in experimental models of Alzheimers disease. Experience in stereotaxic surgery, In-vitro and molecular biology techniques including RT-PCR, Western blot, In-situ hybridization etc. will be preferred. 

PhD, MD, MDS or equivalent degree OR MVSc, MPharm, ME, MTech, with three years of research, teaching and design and development experience, with at least one research paper in Science Citation Index journal

Evaluation of anti-inflammatory and immunomodulatory therapies using in vivo chronic inflammatory and autoimmune animal models such as psoriasis, colitis, and arthritis. Clinical and translational pharmacology focusing on patient-centric drug safety, pharmacovigilance, and outcome-based clinical investigations.

The Director will provide strategic, academic, and operational leadership to the School/Faculty of Pharmacy and Allied Health Sciences. The successful candidate will be responsible for ensuring the highest standards in teaching, research, regulatory compliance, industry collaboration, and institutional development in alignment with national and international academic benchmarks.

Post-Graduation degree, including the integrated PG degree, in any branch of Life Sciences from a recognized university with five years of post-qualification experience of working with mammalian expression, stable CHO cell line or mRNA vaccine platform and strong molecular biology experience.

MSc in Clinical Research or Master in Dental Surgery or Master in Public Health with 1 year post qualification experience in the field of Research or Data handling or Manuscript writing. Prior experience in implementing health projects and/or engaging multiple stake holders and partners, including international agencies. 

Deciphering Chromatin-mediated mechanisms of transcription regulation in Apicomplexan Parasite Theileria annulata. Post Graduate Degree in life sciences OR Post Graduate degree in professional course. M.V.Sc, M.Tech, MSc. Degree in Biotechnology Biochemistry, Microbiology, Immunology. 

PhD in Science, Engineering, Technology or Masters Degree in Engineering or Technology from recognized university/institute Specialization in Biotechnology, Bioprocessing, Biochemical Engineering, Chemical Engineering, Biochemistry, Chemistry or relevant area with two years’ experience

US-FDA, UK-MHRA, WHO, PICS approved, and our products are exported across US, Europe, South America, Asia-Pacific, and Africa.

Product Development of Topical Dosages forms, Parenteral, Injectable forms, Tablet Dosages forms. Basic knowledge about different pharmaceutical dosage forms.

Synthesize, and characterize novel bioactive molecules under supervision of scientist/senior scientist. Knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalyzed reactions, multi-step synthesis.

Sr. Quality Specialist, Clinical Quality responsible for managing clinical quality function, ensuring compliance with local clinical trial regulatory requirements and Takeda Quality Management Systems. Works in collaboration with local clinical operation team ensuring adherence to Good Clinical Practice Guidance.

EVERSANA is a leading independent provider of global services to the life sciences industry. The company’s integrated solutions are rooted in the patient experience and span all stages of the product life cycle to deliver long-term