837 Formulation Development Jobs - Page 34

Develop & refine breeding strategy for hybrid rice with cross-functional teams. Use tech for efficiency, track market trends, lead product development, and travel to field sites for program evaluation & improvement. Required Candidate profile M.Sc. Agriculture (Genetics and Plant Breeding), Ph.D. is added advantage with 15 to 25 Years of relevant exp. Strong people manager with leadership qualities to motivate the team members and mentor

Dear Candidate, We are looking for formulation scientists for our Ophthalmic and Nasal teams in Formulations, focusing on the formulation development of sterile ophthalmic dosage forms solutions, suspensions, and emulsions. This role involves complete ownership of formulation and process development with a strong emphasis on regulatory compliance and timely execution. Position1: Assistant Manager Department: Ophthalmic team - Formulation Development Required Exp : 8-12years Position2: Research Associate/Sr.Research Associate Department: Nasal team - Formulation Development Required Exp: 4-8years(Candidates from injectables background can also apply.) Role & Responsibilities: Formulation & Pr...

Responsibilities: Review IP landscape reports, non-infringement& FTO analysis Devise strategies for patent non infringement and invalidations Collaborate with R & D Scientist to explore design around strategies for P-IV & NCE products Conduct IP due diligence for product selection/ new opportunity identification. Support RA for patent certification, PIL clearances and declaration Monitor, review and manage ANDA litigations Conduct patentability searches, draft and file patent applications and manage prosecutions Ensure timely and effective task delivery through strategic planning prioritisation and execution.

Execution of Development batches. Execution of pre-formulations studies,drug-excipients compatibilities studies & literature. Design and evaluation formulation trials to develop optimize formula. ' Preparation of documents like PDR, MFR,Q&Q.BMR,PVP,PVR,Compatibility protocols and stability protocols, Preparations and management of stability batches. Evaluation and reverse engineering of innovator/refer.ence products. Preparation of technical package of documents fbr DCGI and DCA. Preparations and managenrent of stability batches. Execution ofscale-up and exhibit batches. Execution of technology transfer products and commercial production troubleshooting. A Coordination with others department...

Role & responsibilities Responsible for conducting literature search and preparing literature review presentation. To conduct Physico-chemical analysis of API and preformulation studies. To prepare prototype formulations based on preformulation studies. To optimize Product composition and Processes and prepare batches for Stability Studies. To indent the project requirements like API, excipients, toolings and Packing Materials. Process development, Optimization, validation and successful transfer to manufacturing location. Preparation of process development report. Responsible for the setting up the R&D scale equipment in the Research Laboratory Responsible for checking the calibration of Eq...

KRA: food designing, formulation, and processing. Study the composition of foods to develop methods for safely processing, preserving, and packaging. Analyse and develop new sources of compounds through efficient research.

Sun Pharma is proud to announce the establishment of our world-class Technical Training Academies , a pioneering initiative in our industry. We invite passionate individuals with a zeal for coaching, and training to join us in this transformative journey. Seize this opportunity to enhance your career and shape the future of our organization. Joining our Technical Training Academies not only offers a chance to nurture your passion for coaching but also provides a platform to impact the industry at large. Its an opportunity to grow professionally while shaping the future of technical education in our field. Job Description: Location: Guwahati Technical Training Academy Head overseeing training...

Job Description: Department: Formulation R&D Experience: 3 - 7 Yrs. Qualification: M.Sc / M.Pharma Skills: Should have prior experience and knowledge of development of Soft Gelatin Capsules Technical Documentations - BOM / MFR stability study guidelines , QMS knowledge of pharmaceutical development Technology Transfer to commercial site Should have knowledge of development of other dosage forms (Solid Orals / Liquids /Semi-solids) Good to have knowledge on Nutra / Ayurvedic Regulations

Role & responsibilities Understanding the formulation strategy of competition products, designing approaches for novel skin care technology/formulations, prototype development, shelf-life studies, coordinating with evaluations team for various evaluations, working closely with IP team for patentability of formulations, documentation of technology and conducting technology transfer. Preferred candidate profile Qualifications B.Tech/M.Tech(CosmeticsTechnology) / M.Sc. Chemistry(Organic, Physical, Inorganic, Polymer, Industrial) / M.Sc.(Bio-Technology, Bio-Chemistry) Work Experience : Exposure to personal care product development as an employee 2-6 years of experience in personal care product d...

Qualification: Post-graduate in Pharmacy or Pharmaceutical Engineering Experience: 15 to 20 years in sterile manufacturing plant operations, with a minimum of 10 years in a leadership role and at least 7 years in a regulated sterile manufacturing environment. About The Company Fresenius Kabi Oncology Limited, a wholly owned subsidiary of Fresenius Kabi, is a leading player in the oncology generics market with a broad portfolio that includes injectables, cytotoxic, and APIs. Its state-of-the-art production facility in Baddi features dedicated units for cytotoxic and non-cytotoxic products, including liquid and lyophilized injectables. The facility is approved by global regulatory authorities ...

JOB DESCRIPTION Job Title: Junior Analytical Development Scientist - Injectables Job Location: Bangalore Department : Analytical Development Drug Product About Syngene: Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity quality standards. Driving a corporate cultur...

ORGANISATIONAL OVERVIEW We, Lambda Therapeutic Research Limited are a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad India, with facilities and operations in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA) and Fargo (USA). Over 1500 employees are working across the globe in these facilities. Lambda offers Full-spectrum clinical trial solutions empowered by more than 20 years of service to the biopharmaceutical and generic industry. At Lambda, our gamut of services under the clinical research domain are executed with comprehensive efforts, to deliver positive results. Led by a management team of highly qualified & experienced in...