1057 Formulation Development Jobs - Page 17

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...

Role & responsibilities Formulation Development of Oncology products Exposure of Regulated, Semi Regulated & India Markets FnD Documents like Product development report, , Specifications, MFC,BMR, Stability protocol, CCF , Deviation etc. Awareness of ICH/Regulatory guidelines pertaining to formulation development OSD Experienced candidates willing to work in Onco products can also apply Preferred candidate profile Qualification : M.Pharm with 2-5 Yrs of relevant experience. Interested candidates are requested to share their Cvs on vilshashah@torrentpharma.com

Job Description: We are seeking a highly skilled and experienced professional for the role of Formulation Development OSD , focused on regulated markets including USFDA, MHRA, EMA, and other global regulatory agencies. The ideal candidate will have a proven track record in developing and optimizing solid oral dosage forms (tablets, capsules) for submission and commercial-scale manufacturing. Key Responsibilities: Lead and execute formulation development projects for oral solid dosage (OSD) forms targeted at regulated markets (US, EU, etc.). Design and execute pre-formulation and formulation trials, optimization, and scale-up. Develop robust formulations and manufacturing processes based on Q...

Position Purpose The role holder is responsible for working at the bench ensuring clear and on time delivery of products as planned by the department. This person should be responsible for developing formulations of different actives under the guidance of the Team Leader. The incumbent should be either a M.Sc./MTech/Ph.D. in any branch of chemistry (physical, analytical, agrochemicals, bio-technology). A few years hands-on experience in any organization is an advantage. Key Responsibilities: Strategic Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of R&D Chemistry by driving innovation and team performance according to objectives an...

Job Title : Formulation Development Research Associate OSD (Oral Solid Dosage) Company : Jodas Expoim Pvt. Ltd. Experience : 1 to 5 Years Location : Karakapatla (Hyderabad) – R&D Centre Department : Research & Development – Formulation Development (OSD) About Jodas Expoim : Jodas Expoim is a global, specialty pharmaceutical company engaged in the development, manufacture, and marketing of high-quality injectable and oral dosage form products. We are committed to excellence in innovation, quality, and affordability. Key Responsibilities : Design and develop generic and innovative formulations in the Oral Solid Dosage (OSD) segment (tablets, capsules, granules, etc.). Conduct pre-formulation a...

A Day in Your Life at MKS: As a Chemist at MKS Atotech, you will work in WRC-EN team to support product development and scale-up trials on the pilot line, as well as maintain the pilot line and perform associated activities. In this role, you will report to the Team Manager, WRC-EN. The Chemist will apply various approaches and methodologies to carry out R&D activities related to product development, testing, qualification, troubleshooting, and process optimization under technical guidance. You will work closely with colleagues from your team, the team manager, the R&D manager, and other cross-functional departments. Open and clear communication with the team manager and R&D manager is expec...

Educational Requirements Master Of Comp. Applications,Master Of Engineering,Master Of Science,Master Of Technology,Bachelor Of Comp. Applications,Bachelor Of Science,Bachelor of Engineering,Bachelor Of Technology Service Line Engineering 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, ve...

Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering 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 ...

Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering 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 ...

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...

Educational Requirements MCA,MSc,MTech,Bachelor Of Science,Bachelor of Engineering,BCA,Bachelor Of Technology (Integrated) Service Line Microsoft Practice 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 ...

Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering 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 ...

Responsible for the development and dossier deliverable of genreic application for projects assigned with in the team for Europe ,Canada Australia. Preparation ,review and approval of test licenses Import license applications. Planning and procurement of RMPMs/ RLDs and inventory control at R&D for development. Preparation and review of RMPMs/Justification of Specifications/Cleaning validation report/Risk assessment report/ stability protocol/CDRs/Technology Transfer dossiers. Review of MFRs/BMRs/BPRs/PVPs/HTS, product specific questionnaire, Protocol; and report etc. for scale up and registration batches Timely and Appropriate Reponses for CMC and Bio deficiencies from regulatory agencies f...

Analysis of routine samples (product development batches, stability study samples, raw materials etc.). Operation and Calibration of analytical instruments/equipment s. Analytical activities related to Quality control department. Qualification of working standards. Documentation of analytical activities as per good documentation practices. Work in laboratory as per good laboratory practices. To use PPEs and follow safe practices in lab. Any other task assigned by management. Sampling of raw materials from pilot plant dispensing area. Analysis of samples in quality control laboratory. Operation and Calibration of instruments in quality control laboratory

Role & responsibilities Responsible for finding opportunity for cost reduction. Evaluation of low cost API/RM, taking lab trials and documentation thereof for solid oral products. The candidate is responsible for the scale up and technology transfer at plant scale for identified cost reduction products. Should prepare technology transfer documents and support the filing of the product. Should handle the regulatory queries and support the product launching.