Responsible for upkeep of Encapsulation area in Production and Supervising area in production. Preparation and review of SOPs and other documentation in manufacturing areas.
ANNORA Pharma is committed to provide medicines with highest quality, safety and efficacy that meets the needs of the customers with applicable statutory and regulatory requirements.
Finecure Pharmaceuticals Limited and its subsidiaries are leading manufacturers and marketers of Pharmaceutical formulations and Nutraceuticals in several therapeutic segments in dosage forms of Tablets, Capsules, Oral Liquids, Dry Syrup, Powders, Injections and Sachet.
Lincoln Pharmaceuticals Ltd., Ahmedabad based 40 years old, public limited having presence in 75+ countries, 1700+ registered products, own Manufacturing and R&D center and among india’s top 70 pharma company.
Drug patent expiration presents a significant opportunity for the launch of generic medications, which can dramatically alter market dynamics. When a branded drug's patent expires, it opens the door for generic manufacturers to produce and sell bioequivalent versions at a lower cost, leading to increased competition and reduced prices. This not only makes medications more accessible to patients but also creates substantial market opportunities for generic pharmaceutical companies.
Deciphering the contribution of proestrous-estrous transition to seizure susceptibility in drug resistant epilepsy pathologies. Masters degree in Medical Biophysics, Biochemistry, Zoology, Neuroscience, Biomedical Sciences or any other branch of Life Sciences or M.Pharm Pharmacology.
Diploma in Pharmacy from recognized institute. Should be registered as Pharmacist with the Punjab Pharmacy Council. Candidates should have passed subject of Punjabi upto Matric standard.
Post Graduate Degree in Life Sciences Biotechnology, Biochemistry, Microbiology, Immunology, etc. with 2 years duration and NET, GATE qualification along with 2 years of research experience after Post-graduation in any of following relevant field
An open–label phase II trial evaluating the activity and safety of JDQ443 single agent as first-line treatment for patients with locally advanced or metastatic KRAS G12Cmutated non-small cell lung cancer
Clinical relevance of mitochondrial signaling in pediatric intraocular malignancy project funded by ANRF Erstwhile SERB-DST for a period of 3 years in the Department of Pediatrics.
Your function in ensuring data accuracy is critical. You’ll validate ingredient information and toxicological data to maintain consistency across products and platforms. You will connect these elements by adapting to the evolving landscape of consumer safety and seeking innovative ways to manage and communicate ingredient data.
Exposure of analysis for Finished Products, Stability Samples and Raw Materials. Having Knowledge of Analytical Method Validation, Verification and Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals and Quality process.
Responsible for monitoring and ensuring quality of products and comply with cGMP standards. Monitoring of critical process parameters, line clearance before batch initiation, verification of RM and equipment. In process sampling for quality check like pH, moisture content, and reaction monitoring.
Pharma Graduate with 2-8 years of experience in tablet and Liquid sterile manufacturing and Production QMS. Track and Trace systems, Manufacturing, Compounding of Nasal Spray formulations, vial Washing and filling machines. Having Good experience on online documentation and Knowledge to work in GMP environment.
Expected B.Pharm, M.Pharm, M.Sc, B.Sc by education with 2 plus years experience in Vial, Ampoule, Sterilizer, Tunnel & Washing, Component GMP wash & dry, Filling & Sealingarea and Documentation
Line clearance activity for Washing, Filling, Sealing, Visual inspection. Performing Environmental monitoring activity in Grade A, B, C and D clean room area. In process activity.
The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
Novartis announced that it has entered into an agreement to acquire Regulus Therapeutics, a San Diego-based, publicly traded clinical-stage biopharmaceutical company focused on developing microRNA therapeutics. Regulus’ lead asset, farabursen.
Researchers have uncovered multiple new genes and genetic pathways that could lead to repurposing hundreds of existing drugs for osteoarthritis, the most common form of arthritis. The research, which analyzed data from nearly 2 million people in diverse populations worldwide, was recently published in Nature. It represents an extensive genetic exploration of osteoarthritis, a condition affecting over 600 million people globally.