21 F&D Jobs

Literature review of Raw materials. Procuring input materials and intermediates for F & D New product development. Improvement in quality of existing products. Documentation of entire product development cycle. Required Candidate profile Technology transfer Complaint handling & investigation Getting in touch with marketing department for new product/improved product feedback Technology transfer from F & D to Pilot or commercial batch

product development - tracking and monitoring of IIDs within the define timelines. co-ordination with in-licensing / F&D / ADD / QA team on the progress of the project tracking & reporting of all new developments Required Candidate profile 2-4 years of experience in F&D or ADD with interest in Project management or experience in Project Management pharma OSD.

We are expanding our team!! Looking for passionate Formulation Scientists (Product Development group) for Regulated market at our dedicated R&D center. Department : Formulation Development (Product Development group) Formulation : Solid Orals / Injectables Market : Regulated Experience Required : 2-6 years Location: R&D Center, Moraiya, Ahmedabad. Job Profile (Not Limited to): 1. F&D - Oncology (Injectables) Development of activities of Onco injectable formulations for Regulated Markets (US & EU Markets). Additional experience in CA markets is preferable. Candidate must have sound knowledge of different techniques like liquid injectable (solution formulation, suspension emulsion formulations...

Opening for Formulation and Development. Location : Mehemdabad ( Kheda) Role & responsibilities : Formulation Development: Develop new ointment formulations and improve existing ones. Select appropriate excipients based on compatibility, functionality, and regulatory acceptance. Conduct pre-formulation studies, solubility, and stability assessments. Prepare lab-scale and pilot-scale batches. Process Optimization: Develop and optimize manufacturing processes (mixing, homogenization, filling, etc.). Prepare process validation and scale-up documents. Documentation: Prepare and maintain formulation development reports (FDRs), batch manufacturing records (BMRs), and specifications. Support dossie...

Role & responsibilities Lead product development and manufacturing practices with focus on quality and continuous improvement. Design strategic plans and set organizational growth goals. Manage budgets and optimize expenses. Ensure employee motivation and productivity. Oversee project work, facility layout, and qualification activities. Conduct periodic training for formulation personnel to enhance product and productivity. Maintain effective communication with relevant stakeholders. Perform additional assignments with commitment to safety practices. Stay updated on global innovations and industry trends. Prepare weekly, monthly, and quarterly reports. Monitor daily manpower and work distrib...

We are looking for ADL , F&D and , QA , QC stability , Packaging & Development Required Candidate profile Location: Sanand Hamlai Industries Pvt. Ltd. AV-25, Bol Industrial Estate, Sanand – II, Ahmedabad, Gujarat-382170 Qualification: Mpharm / M.sc Experience: 3 to 5 yrs

1) Understand and develop immediate release and modified release oral formulations for regulated markets (US and EU market); 2) Handling equipment’s for solid oral dosage forms. 3) Troubleshoot in existing products and optimize the process; Required Candidate profile 4) Knowledge of using Design Expert/Mini Tab QbD Software for development conduct experiments. 5) Preparing reports like PDR, specifications, stability protocols, DoE, Tech transfer & Reports.

Planning and coordinating with project management team, regulatory affairs, analytical development and management team Pivotal involvement in product pre-formulation study and prototype formulation development Preparing reports, compiling/interpreting data and validating stability data of developmental batches Key role involvement in a vast gamut of activities encompassing - formula & process optimization, monitoring scale-up batches, validating batches for regulatory markets; adhering to regulatory markets like ROW standards and so on Responsible for executing site transfer projects from contracts like Bells, Teva, Relonchem and Nova Involved in evaluating Critical Quality Attribute (CQA) &...

Role & responsibilities Coordinate with formulation scientists for day-to-day activities, designing formulation strategies, execution of laboratory trials and preparation of technical documents for sterile dosage forms Coordinate with other technical staff responsible for testing new drug substances, excipients, pre-formulation samples, and formulation development samples. Ensure the timely completion of new product development of sterile dosage form. Interact with Manufacturing, Validation, and Materials Management teams to ensure smooth drug product development and transition to commercial-scale manufacturing. Manage all activities associated with registration batch manufacturing, includin...

Position: AM_ ADL Key Requirements: Conducting in-depth Literature and patent search and making formulation development plan for Solid oral and Liquid oral formulations Develop new formulation concepts, assists in the development of project plans, business analysis and feasibility assessments. Develop experimental programs, work plan and prioritize assignments to meet project objectives within defined timelines Review and analysis of experimental data and design of further experiments. Monitoring of stability studies and Data interpretation Formula and process optimization studies - Discussion/design, review and monitoring of PET trials, pH Establishment Trials and PDR Trials Identify and ma...

Role & responsibilities 1. Formulation & Development for Emerging Market & Regulated Market 2. Execution of Lab Trial batches & Tech Transfer activities at site. 3. Lab note book writing & documentation ensuring compliance with regulated guidelines. Preferred candidate profile Experience in Tablet, Capsules, Pellets, ER, SR and DR product development for emerging market M.Pharm Only

Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientists for DOM/EMB market at our dedicated R&D c...

Studies, and process optimization as per regulatory guidelines (USFDA, EU, WHO). Prepare and review development reports, PDRs, BMRs, MFCs, and technology transfer documents. Collaborate with cross-functional teams (QA, QC, RA, Production).

Location: Sanand Hamlai Industries Pvt. Ltd. AV-25, Bol Industrial Estate, Sanand – II, Ahmedabad, Gujarat-382170 Qualification: Mpharm / M.sc Experience: 3 to 5 yrs

To perform trials for new products ,Preformulations studies, In process development and testing for Nutraceutical and probioceuticals in different dosages forms (Powder / Tablet/capsule/liquid doses form).

Drive development of innovative probiotic, nutraceutical, herbal and natural-based formulations Align R&D strategy with business goals Work on solid orals, sachets, liquids, and novel delivery systems Lead a young dynamic team of R&D scientists Required Candidate profile Decent experience in probiotic/nutraceutical/innovative formulations Passionate about creating breakthrough, evidence-backed products

Position of Formultion and developments for Nutraceutical and probioceuticals in different dosages forms (Powder / Tablet/capsule/liquid doses form). To perform trials for new products ,Preformulations studies, In process development and testing,

WALK-IN INTERVIEW ALERT JD Join the growth journey with Opes Healthcare Location: 3rd Floor,Tulsi Plaza, Changodar, Ahmedabad. Date: 25th May 2025 (Sunday) Time: 09:00 AM to 02:00 PM Multiple Job Openings at Opes Healthcare-Ahmedabad. Were hiring passionate and dynamic individuals across multiple departments! Open Positions: 1. IPQA :Monitor all process check/Line Clearance/cGMP/Documentation Officer to Sr. Executive. B.Pharm/ M.Pharm | 02–07 yrs 2. Quality Control: RM Testing/HPLC/GLP/Documentation – Officer to Sr. Executive. B.sc/M.sc/B.Pharm/ M.Pharm | 02–07 yrs 3. F&D: Design & Develop formulation/Process Optimization/cGMP/Documentation/ – Officer to Sr. Executive. B.Pharm/ M.Pharm | 02–...

MJ Biopharm has two manufacturing locations . Our Facility located in Taloja, near Mumbai, is WHO GMP Certified, state-of-the-art facility . Other facility Facility is in Pune

Candidate should be experience in Complex Injectable dosage form such as Liposomes, Microspheres, Nanoparticles, polymeric multi-particulate systems, Depot formulation, Suspensions, Lyophilized powders, colloidal suspension, and peptides.

Formulation And Development Executive F&D develop new formulations in line with the marketing requirements Product development plan, execute and monitor Formulation and development, extractable, leachable studies and diluents compatibility studies Required Candidate profile Formulation And Development Executive F&D 4 year + experience in OSD or Injectables Perks and benefits Best in Industry*