Masters degree in Pharmacy or Pharmaceutical Chemistry or Pharmacology or Chemistry or Biochemistry or Bacteriology or Medicine or Microbiology or Biotechnology; in the Regional Drugs Testing Laboratory, Guwahati, CDSCO, DGHS, Ministry of Health and Family Welfare.
ECHS Unites application to engage the following vacancies Medical. Para Medical & Non Medical Staff on contractual basis in 02 x Polyclinic. Devlali and Dhule for a period of one year renewable for additional period of one year/ till attaining the maximum age subject to performance of candidates/ other conditions according to the criteria as mentioned against each post :
M.S (Pharm)/ M. Pharm/ M.Sc in Pharmacy/ Biomedical Engineering, Biotechnology; The project involves development of synthetic tracheal tubes, evaluation of in vitro cytotoxicity and in vivo biocompatibility in animal model.
M.Sc. In Biochemistry/ Pharmacology/ Biotechnology/ Life Scienccs or equivalent with two years of research experience or M.Tech. Study of selected Ayurvedic herbs for their anti-angiogenic potential and toxicity profile in zebrafish embryo model for cancer management.
Development and Evaluation of the Effectiveness of Improved Take-home Foods in Combination with Behaviour Change Intervention to Improve Nutritional Status. in Children in Selected Districts of Six States of India, A Cluster Randomized Controlled Trial
PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.
Post : Senior Regulatory Affairs Associate (Labelling)
M.Pharm/B.Pharm/M.Sc/B.Sc; IPQA/APQR/Validation and Qualification; Handling Change Control/ CAPA/ Deviation/ Investigation and Audit Management; Issuance and Retrieval of GMP Document
Centaur Pharmaceutical is the largest specialty of drug manufacturing Organization. We provide high quality affordable medicines trusted by healthcare professionals like USFDA and MHRA. We are one of the rapidly growing Pharmaceutical Company in India. To keep pace with our growth plan, we required young and energetic professionals for our Pune site, having experience in Formulation / Oral solid dosage.
Ph. D, MD, MS, MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc, M.Pharm, ME, M.Tech with at least one research paper in Science Citation Indexed journal.
Passed Madhyamik, Secondary from a recognised Board and Diploma, Certificate course in Ayurvedic Pharmacy, Homeopathic Pharmacy conducted by the Paschim Banga Ayurved Parishad, Council of Homeopathic Medicine, West Bengal.
To visit medical professionals and promote company products as per the company strategy by generating prescriptions. To visit chemists and Stockists and ensure availability of the products.
Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca'a API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.
To provide scientific support to analysts at bench level for developing & qualifying methods required for product Analytics. Execution of critical experiments for specific deliverables.
Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs. Hetero business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.
The ideal candidate will ensure smooth running of multiple cell-based and biochemical assays while maintaining highest quality and integrity of data and meeting established timelines.
You will be responsible for generating new product ideas from Key Opinion Leaders interactions, prioritizing these ideas, preparing business cases, analyzing market and competitor data, and handling creative aspects like branding. The aim is to ensure the timely launch of products that address unmet market needs.
Celebrating Life Sundyota Numandis, our name, truly defines our purpose of existence. It means A sparkling expression of joy, empowered by the cosmic energy of the Sun.
Works closely with the Global Regulatory Lead, Regulatory Affairs Manager providing the submission strategy and with the Submission Manager executing the submissions.
In this role, you will perform coding activities on the assigned project in a timely and efficient manner, code the Medical Conditions and Medication terms in the Coding tool, generate Queries to clarify in order to facilitate coding, and participate in study related meetings as needed.