816 Formulation Development Jobs - Page 26

Preferred candidate profile : Experience or Education in Pulp , Paper and Cellulose Technology Experience Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, D...

Design and develop formulations for generic drug products (solid orals) Experience in technology transfer Prepare and review Master Formula Records (MFR), Batch Manufacturing Records (BMR), and technology transfer documents.

Role & responsibilities Lead Pre Formulation studies for solid orals, oral liquids, external preparations, injectable products, and nutraceuticals. Design project strategies through comprehensive literature surveys. Conduct API and excipient characterization, drug and excipient ratio studies, and explore various manufacturing strategies. Develop and finalize QQ formulas in alignment with the requirements of the Business Development (BD) team. Coordinate with BD team to ensure timely project execution. Finalize specifications for finished products. Evaluate product stability during manufacturing, monitor stabilized batches, and prepare related reports. Enhance existing formulations and explor...

Looking candidates for PDR (Formulation & Development ) Dept. 2-7 years of relevant experience in solid oral dosage (Regulated Market) Roles and Responsibilities 1.Candidate should perform literature search 2.Pre formulation development Required Candidate profile 1.knowledge of documents – Master formula card, Bill of Material, stability protocol 2.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

To involve from start and investigate level 2 & 3 incidents, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing. To Involve in valid OOS and other cases as relevant, by working closely with site CFT and operating people to arrive at proper Root cause, CA and PA and in report writing. To review level 1B incidents and give feedback for improvement. To periodically trend level 1A incidents and highlight/escalate key observations. To review any other referred reports associated with incidents/events in association with sites. To possess high level of integrity to have unbiased, independent and objective closure of incidents and m...

Role & responsibilities Experience: 3-6 years Specialization: soft gel Key Responsibilities: Formulation Development : Design and optimize Softgel formulations for pharmaceutical and nutraceutical applications. Process Optimization: Conduct proof-of-concept studies, scale-up trials, and technology transfers. Regulatory Compliance: Ensure formulations meet ICH, FDA, and GMP guidelines. Analytical Coordination: Work with analytical teams to develop and validate testing methods. Troubleshooting: Address formulation challenges related to solubility, stability, and encapsulation. Documentation: Maintain accurate records, prepare technical reports, and contribute to regulatory submissions. Collabo...

Responsibilities: Responsible for formulation and process development of Injectable dosage forms. Troubleshoot and problem-solve unresolved or new formula issues. Design and execute formulation trials to finalize formulation composition. Provident fund

1. Product development: Utilize extensive experience in the pharmaceutical industry to lead comprehensive reviews of literature, evaluation of finished products, and acquisition of scientific insights. Conduct pre-formulation trials, laboratory experiments, and meticulously document findings in detailed reports. Oversee lab and scale-up trials with precision, ensuring seamless execution while meticulously preparing all necessary documentation and reports. Take charge of preparing protocols, batch records, and other essential documents to maintain stringent quality standards. Lead process evaluation, exhibit batch execution, and prepare comprehensive reports with meticulous attention to detai...

Medicamen Biotech - SRL Pharma R&D Centre Required Formulations Profile Designation: Executive/ Scientist Qualifications: M. Pharma - Pharmaceutics Vacant Post: 6 Nos. Experience: 4 to 8 Years Please share profile on uday@shivalikrasayan.com Required Candidate profile Pharma R&D experience must in Formulation USFDA exposer prefer Preparation of Pharmaceutical Development Report Ready to relocate Bhiwadi, Rajasthan Ready to join Immediately Prefer Team Player Perks and benefits Best of Industries Salary based on Experience

Qualification: Candidate must have a background in a Diploma in Pharmacy or a Bachelor of Pharmacy Role & responsibilities Possess sound knowledge of pharmaceutical excipients, active pharmaceutical ingredients (APIs), and the complete tablet manufacturing process. Well-versed in the technical aspects of generic formulations and common practices in tablet manufacturing. Ability to assess and understand the impact of ingredient combinations on the final tablet output and performance. Capable of working independently with design and technical teams, providing front-end technical support, troubleshooting issues, and offering practical solutions. Willingness to travel across India with the techn...

Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertic...

Role & responsibilities To review and understand technology of product from R&D scientist and coordinate, plan activities with all concerns personnel/ dept. for successful transfer of the products, Monitor tech transfer at site and update documents. To review and understand technology of product from CRO and coordinate, plan activities with all concerns personnel/ dept. for successful transfer of the products, monitor tech transfer at site and update documents. To resolve manufacturing issues/trouble shooting batches at manufacturing sites for the products which are commercialized. Monitoring of redeveloped formulations for quality improvement at manufacturing site. To develop new products a...

Roles and Responsibilities Develop new products by leading cross-functional teams through formulation development, process development, and scale-up. Collaborate with external partners (CROs) on OSD product development and registration dossiers preparation. Ensure compliance with regulatory requirements for solid oral products at CDSCO and DCGI. Manage budgets, resources, and timelines for R&D projects to achieve business objectives. Desired Candidate Profile 15-18 years of experience in pharmaceutical industry with expertise in AR&D. Bachelor's degree in Pharmacy (B.Pharma) followed by Master's degree (M.Pharma). Strong understanding of formulation development, formulation research, Nutrace...

Roles and Responsibilities Develop and implement new product ideas through CDSCO process. Oversee research and development projects from concept to commercialization. Collaborate with cross-functional teams to ensure successful project delivery. Ensure compliance with regulatory requirements (DCgi) and maintain high standards of quality control. Desired Candidate Profile 15-18 years of experience in pharmaceutical industry, preferably in FR&D or similar role. B.Pharma degree in Any Specialization; M.Pharma preferred but not mandatory. Strong understanding of formulation development, formulations, nutraceuticals, OSDs, and solid orals.

Job Title: F&D Executive Experience: 23 Years Department: Formulation & Development (F&D) Location: Prahladnagar, Ahmedabad Reporting To: F&D Manager / R&D Head Job Description: We are looking for a skilled and detail-oriented F&D Executive with 2–3 years of hands-on experience in pharmaceutical formulation development. The ideal candidate should possess a solid understanding of global regulatory guidelines (e.g., ICH, USFDA, EMA) and strong expertise in dissolution method development. The role involves supporting product formulation, optimization, and technology transfer activities in line with international quality and compliance standards. Key Responsibilities: Develop and optimize formul...

Amneal Pharmaceuticals is looking for Officer, Process Development to join our dynamic team and embark on a rewarding career journey Develop and optimize manufacturing processes Support trials, validation, and scale-up activities Analyze data to improve yield and efficiency Ensure compliance with regulatory standards

Role & responsibilities Formulation Research And Development (FRD): Executes and supports formulation research & product development activities of the company to meet the pre-determined goals. Develops the formula based on information collected through literature search, innovator product details, pre-formulation studies and requirements as applicable for product and process design. Studies the effect of changing levels of key excipients such as taste masking agents, film formers, disintegrants, plasticizers etc. to establish the robustness of formulation. Finalization of excipients along with specifications and the finalized formula to yield a satisfactory physical and chemical properties i...

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,

Role & responsibilities To formulate and conduct evaluations and due diligences related fragrancing products including deos, perfumes, talcs and emulsion products. Product Development Activities: Literature Survey, Batch Making, Stability Studies, Product Analysis, Sensory Evaluation, Documentation Preferred candidate profile Qualifications : Masters in Chemistry/ Bio Chemistry/Cosmetic Technology Work Experience : 2-4 Experience in personal care FMCG industry & Experience in formulation development of fragrancing products/ personal care (alcoholic base, emulsions and coloured products) including Deos, perfumes, antiperspirants, fine fragrances etc. Skills : Sound understanding of Personal C...

Purpose of the job Accountable for: Efficient contribution to Tender execution (including TT Agreements) over Transfer Activities (S,D). Efficient contribution to Project execution over Transfer Activities (S,D,R). TT processes and tools deployment and improvement (S,D,R) . Efficient Data sharing with Transfer Stakeholders (Donor/Receiver; Project/Metiers/Sites) (S,D,R). Position in the Organization Organization Structure See standard PME organization chart. Organizational Reporting Reports hierarchically to the Site PME Manager Reports operationally to the Project Manager Reports functionally to the TT Process Owner Team (*depends on scope) People (*): 0 direct report Network and links Indu...

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 (...

Key Responsibilities: Product Development & Sensory Innovation Lead the formulation, pilot trials, and commercialization of innovative premix and dry-mix nutraceuticals. Develop and refine flavour profiles using botanicals, bioactives, and natural essences. Conduct structured sensory evaluations and reduce rejection rates through scientific feedback integration. Scientific Research & Market Insight Track global and regional market trends to drive innovation and new product ideas. Conduct literature reviews, ingredient functionality studies, and competitive benchmarking. Generate a robust product pipeline aligned with functional and clean-label trends. Process Optimization & Scale-Up Lead pro...

Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertic...

Work Experience (Total number of years/ experience/ background or equivalent) : Total experience (in years): 15 Experience in current role (in years): 6.5 Years Work Background: Formulation Development, Technology Transfer, Root Cause Investigations, Project Management Primary Job Function - To drive technology transfer for Third party manufacturing, Loan license projects, Abbott s own manufacturing plants. To support Abbott site MS&T team as per requirements. To support Alternate supplier qualification of raw materials & API. To comply with the regulatory, quality, statutory, EHS and Pharmacovigilance requirements. Core Job Responsibilities - To perform effective gap analysis between sender...

Role & responsibilities 1. Formulation & Development for emerging & regulated market. 2. Execution of Lab Trial batches & Tech Transfer activities at site. 3. Lab note book writing & documentation ensuring compliance with regulatory guidelines \ Preferred candidate profile - Experience in Tablets, Capsule, Pellets, ER, SR, and DR product development for emerging market.