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4.0 - 6.0 years
5 - 7 Lacs
Ahmedabad
Work from Office
Role & responsibilities Prepare, review and submit regulatory documents for new drug applications, product registrations, amendments and renewals to the US, Brazil, EU, India and State Level authorities. Regulatory Submissions : Prepare and submit regulatory documents, including INDs (Investigational New Drug Applications) and NDAs (New Drug Applications) to regulatory authorities. Compliance and Licensing: Ensure compliance with regulatory requirements of US, Brazil, EU & India. Liaise with regulatory authorities for drug licensing, including product registrations, renewals and manufacturing licenses for local and international markets. Ensure timely submission of import licenses and NOcs (...
Posted 5 months ago
3.0 - 6.0 years
5 - 7 Lacs
Pune
Work from Office
Role & responsibilities 1) Candidate should have understanding and experience in development of different types of oral dosage forms like immediate release formulation/delayed release formulations/ pellet coating and controlled release formulation,hard gelatin capsule, soft gelatin capsules, solutions, suspensions, dry powders and syrups for different Regulated and semi regulated markets. 2) Carry out pre-formulation and formulation development experiments for new chemical entities and ANDA formulations. 3) Develop new technology platforms and conduct feasibility studies for novel formulations such as microspheres, pellets, and spherules, aqueous and non-aqueous suspensions, ophthalmic and s...
Posted 5 months ago
2.0 - 4.0 years
3 - 6 Lacs
Navi Mumbai
Work from Office
Role & responsibilities Conduct competitive intelligence searches for understanding the competitive landscape for API pellets, granules technology and identifying opportunities for pellets business. Conduct patent searches for API pellets technology and identify blocking patents. Conduct patent infringement analysis of API pellets. Prepare report on global launch scenario for APIs through patent expiry status and regulatory exclusivity status. Tracking patent alerts for the in-house products, and studying the retrieved patents updates and communicating with R&D for feedback. Analyse customer patent queries on APIs/KSMs and draft responses to the queries.
Posted 5 months ago
7.0 - 12.0 years
7 - 9 Lacs
ahmedabad
Work from Office
Job Title: Senior Manager Formulation Development (Generic Finished Formulations) Department: Research & Development (R&D) Formulation Development Reports To: Head – Formulation Development / Vice President – R&D Job Purpose: To lead and manage the development of generic pharmaceutical finished dosage forms (oral solids, liquids, injectables, topical, etc.) from concept through scale-up, technology transfer, and regulatory submission. Responsible for ensuring robust, cost-effective, and regulatory-compliant formulations aligned with company strategy and market requirements. Key Responsibilities: Formulation Development & Optimization Lead the design and development of generic formulations fo...
Posted Date not available
8.0 - 13.0 years
6 - 9 Lacs
navi mumbai
Work from Office
Role & responsibilities 1. Development of stable, bioequivalent pellets dosage form (IR/ SR/ DR/ ER/ MUMPS) 2. Efficient technology transfer of pellets projects from R&D to plant level. 3. Closely working with Plant tea for trouble shooting of ongoing commercial pellets projects. 4. Oversee all aspects of pellets dosage form including planning, execution, and innovation strategy. 5. Evaluation and implementation new technology for pellets product development. 6. Collaborate with internal team and external partners for project success. Preferred candidate profile 1. Strong expertise in pellets dosage product development and its technology transfer to plant. 2. Strong analytical and problem-so...
Posted Date not available
12.0 - 20.0 years
8 - 10 Lacs
hyderabad
Work from Office
Proven experience in a managerial role within engineering and maintenance operations, preferably in pharmaceutical manufacturing environment hands-on experience with process and engineering services and utilities Basically in Pellets or Formulation Required Candidate profile Knowledge of safety standards, regulatory requirements, cGMP guidelines applicable to pharmaceutical manufacturing. Strong problem-solving abilities Prior experience in pharmaceuticals 6 days working
Posted Date not available
3.0 - 7.0 years
8 - 10 Lacs
nashik, aurangabad
Work from Office
Location: North Maharashtra - Nagpur & Vidarbha ( Nashik & Aurangabad) Key Purpose of the Role: Develop a network of Biomass processors and suppliers: briquette/ pellet manufacturers, industries with biomass by-products and other related entities Sell subscription to the platform, ensure active participation of the customers, increase engagement for greater share of their business, sell value added services, generate revenue. What Key Tasks will be involved?: Supply Network Development Identify suitable Supply Entities to be targeted and work on leads developed by marketing initiatives (Briquette makers, pellet makers & Industrial Biomass Suppliers) in operating areas defined as area of resp...
Posted Date not available
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