796 Formulation Development Jobs - Page 6

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S. Bhartia and Mr. Hari S. Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research and Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Group has global presence employing around 42,000 people across the globe with over 2,400 in North America. Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, Contract Research...

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...

Consultant – FDA & Intl Pharma Compliance | 20-25 yrs exp in USFDA/MHRA/WHO GMP, audits, DMF/CTD, QMS, validation & formulation (solid, liquid, semi-solid, injectables). Mentor QA/QC/R&D, guide compliance for global markets.

We required candidate for the position of AGM-Formulation Exp in OSD-Immediate Release (IR),Extended Release (ER),Powder for Suspension(PFOS) &Oral Liquid dosage forms for US,EU&Canada. T-Exp-15 + CTC-Upto 30.00Lacs Loc-Mumbai(Kandivali)

As a Formulation Development Scientist at our company, your role will involve developing and optimizing skincare and cosmetic products such as creams, gels, serums, lotions, balms, masks, and color cosmetics. You will base your formulations on brand briefs, market trends, and performance goals to ensure product efficacy and success. Your responsibilities will include: - Conducting Stability & Compatibility Testing: You will be responsible for conducting physical, chemical, and microbiological stability studies to ensure product safety and efficacy throughout its shelf life. - Sampling & Trials: You will prepare lab-scale and pilot batches, record detailed trial reports, and assist in process...

Role & responsibilities Post- R&D Manager Location - Pune Kondhwa Industry - Induatrial Coating and Painting Automotive Email - punejobs02@gmail.com Education - BE / DME Mechanical , MBA Experience - 08-12 yrs CTC - 8.00 - 12.00 LPA SKils R&D (Research & Development) Manager is responsible for overseeing and leading a team in the design, development, and implementation of new products, technologies, and processes. This involves: 1. Setting R&D strategy and goals in alignment with the overall business strategy. 2. Allocating resources, including people and funding, to R&D projects. 3. Collaborating with cross-functional teams, such as engineering, marketing, and sales. 4. Overseeing product t...

Responsibilities: * Develop new formulations for nutraceuticals, advanced probiotics, and herbal products * Handle equipment for solid, liquid, and semi-solid dosage forms

Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requiremen...

Educational Requirements Bachelor of Engineering Service Line Enterprise Package Application Services Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes a...

Responsibilities A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requiremen...

As a Principal Analyst, you will be part of our deliverability team working directly with our customers. You will provide guidance on best practices, reporting and recommendations to improve their email programs and get the most out of Zeta Global. Teams at Zeta work collaboratively to deliver great customer experiences. You will partner with our Client Services, Technology and Sales Teams to develop strategies that improve both our customers and our teams. Job Description Provide guidance to clients to improve deliverability for their email programs Support an assigned portfolio of paid deliverability services clients Own the client relationship for your portfolio Manage onboarding projects...

Role & responsibilities Nitrosamine and regulatory query support Conduct nitrosamine risk assessments for APIs, excipients, packaging components, and finished drug products. Evaluate manufacturing processes, raw materials, and excipients for nitrosamine risk. Review current regulatory guidelines (ICH M7, EMA, USFDA, CDSCO, WHO, and other ROW countries) and apply them in assessments. Prepare risk assessment and justification reports for internal and regulatory submission. Work with Analytical Development, Quality Assurance, Regulatory Affairs, and Formulation teams to collect and interpret required data. Support confirmatory testing strategies and assist in root cause investigations if nitros...

We re seeking a passionate and proactive individual to develop breakthrough product solutions grounded in deep consumer insight and market foresight Key expectations from the role are CORE: Key requirement of the role is to work on innovation / renovation / value improvement projects for both product process development, and technology transfer The person should design and develop innovations, renovation and cost-saving projects for Tea (Black, Green, Instant), Coffee (RG, Instant, Beans), and premixes formulations, aligned with business briefs Consumer understanding: Translate consumer habits and insights into product attributes, develop hypotheses, and validate through testing Conduct comp...

As a Formulation Manager for the Generic Market Support in the pharmaceutical industry, you will play a crucial role in leading laboratory operations, managing technical support, and collaborating with cross-functional teams to support pharmaceutical applications across Asia Pacific, Latin America, and the Middle East. **Key Responsibilities:** - Oversee formulation development and technical support for pharmaceutical applications in regulated markets. - Collaborate with business development and R&D teams to enhance pharmaceutical formulations. - Provide scientific support to internal teams, distributors, and clients. - Manage laboratory operations, ensuring adherence to timelines and budget...

As an R&D Chemist at our company, you will be an integral part of the Research & Development team. Your role will involve developing and optimizing formulations, conducting lab-scale experiments, and supporting innovation in product and process research. A strong foundation in chemistry and a hands-on approach to lab work and documentation are essential for this position. Key Responsibilities: - Develop and optimize formulations for various products - Conduct lab-scale experiments to test new ideas and processes - Support innovation through research on product development and improvement - Maintain accurate documentation of experiments and results Qualifications Required: - Bachelor's degree...

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.

As a Material Engineer at the Material Technology Cell (MTC) in the Research & Innovation Centre in Noida, your role is crucial in advancing material research, testing, and development to foster innovation across the product portfolio. You should be technically proficient, research-driven, and possess strong analytical capabilities with hands-on experience in polymer characterization. A collaborative mindset is essential to thrive in the multidisciplinary R&D environment. Key Responsibilities: - Conduct material testing and characterization using advanced techniques and equipment such as DSC, TGA, FTIR, and optical microscopy. - Prepare polymer samples and conduct structured analysis to faci...

lead&plan projects-pellets/mups,meet TPP, timelines,budget-FRD(FBC,RMG,Coating,Nano),interpret ARD results,delegate & monitor teams, Ensure compliance: MFR,scale-up,stability protocols,PDRs,SOPs,GMP,SHE Technical discussions-DQA, ARD, Marketing, Required Candidate profile FRD pellets/modified release, QbD,cGMPs, GLPs, expertise in process and formulation optimization,tech transfer&scale-up -FBC,RMG,coating,extrusion,nanotech, DIPO qualification, validation, spec review

develop/optimise pellets/mups - FRD(FBC,RMG,Coating,Nano),interpret ARD results,delegate & monitor teams, enforce GLP&GDPs, prep/review: MFR,scale-up,exhibit & stability protocols,PDRs, SOPs cross-function coordination, meet TPP, timelines,budget. Required Candidate profile FRD pellets/modified release, QbD,cGMPs, GLPs, expertise in process and formulation optimization,tech transfer&scale-up -FBC,RMG,coating,extrusion,nanotech, DIPO qualification, validation, spec review

Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures. Manage clinical and third-party data reconciliation based on edit specifications and data review plans. Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management. Address data related questions and recommend potential solutions. Identify root cause to systematically resolve data issues. Your profile Bachelors degree in a relevant field, such as Life Sciences or Healthcare. Intermediate kNwledge of clinical data management within the pharmaceutical or biotechNlogy industry. Familiarity with data management s...

Main Accountabilities Routine analysis & Stability Analysis (assay, RS, dissolution, water content etc.) of R&D formulation projects (solid & liquid orals, injectables) Daily calibration of pH meters, balances etc. Stability sample management (loading & withdrawal as per stability plan) Preparation of Stability Reports & other protocol based study reports for assigned projects, as applicable Hands-on experience of analytical instrumental techniques (HPLC with chromatographic software etc.) Assisting analytical method development/validation/method transfer activities, as per need Supporting other assigned lab responsibilities for GLP compliance Performance Indicators: Timely execution of assi...

Location: Ahmedabad Qualification: M.Sc./Ph.D. (Organic Chemistry) Experience: 0-6 months Job Description: Assist senior scientists in carrying out experiments related to API, CRO, and CDMO projects. Perform basic laboratory activities such as reaction setup, sample preparation, and documentation. Support in maintaining lab safety standards, equipment handling, and record keeping. Learn and apply analytical techniques under guidance. Skills Required: Strong academic knowledge of Organic Chemistry. Willingness to learn API process research and development. Good communication and documentation skills. --- 2. Executive / Sr. Executive R&D (API/CRO/CDMO) Location: Ahmedabad Qualification: M.Sc./...

Job Location: Bangalore Department: Analytical Development Drug Product About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productiv...

Job Title: Advanced Scientist Summary: Advanced IP Scientist based at the Momentive Corporate R &D Centre in Bangalore will work closely with the Momentive Technologists globally attending to their requests for IP Search and Analysis. The IP Scientist would also assist the technologists by disseminating awareness on internal IP processes and strategies as well as information that could promote innovation. IP Scientist will perform IP search and Analysis to generate IP insights across Business segments and Business divisions of Momentive, attend to office action responses and support in overall IP management of the Technology IP team. The IP Scientist will be directly and independently respon...

As a Trainee/Executive - R&D at Abha Biotechnology Pvt. Ltd, you will be part of a premier contract manufacturing company specializing in liquid, solid, and powder dosage forms for nutraceutical and health supplement products. Your role will involve assisting in planning and conducting experiments to develop new products or improve existing formulations. You will also be responsible for performing laboratory-scale synthesis, analysis, and validation of biochemical or pharmaceutical products. Analyzing experimental data and preparing detailed technical reports will be a key aspect of your responsibilities. Maintaining accurate and detailed records of all research activities and experiments is...