80 Solubility Jobs - Page 2

Job Description: Job Title: Intern – CMC (Formulation) Duration: 12 Months (1 year) Location: Hyderabad Department: CMC (Formulation) Reporting To: Lead Scientist - CMC (Formulation) Stipend: Paid Qualifications: Master’s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution. Strong academic background in pharmaceutics Basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage. Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing. Excellent communication, organizational, and problem-solving skills. Position Summary: The Formulation R&D Intern...

Job Description: Job Title: Intern – CMC (Formulation) Duration: 12 Months (1 year) Location: Hyderabad Department: CMC (Formulation) Reporting To: Lead Scientist - CMC (Formulation) Stipend: Paid Qualifications: Master’s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution. Strong academic background in pharmaceutics Basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage. Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing. Excellent communication, organizational, and problem-solving skills. Position Summary: The Formulation R&D Intern...

Job Title CMC-IRA Job Grade G11B/G11A Function India Regulatory Affairs Location: Baroda Job Summary Review of CMC documents. Documents include but not limited to following: Drug Substance Structural formula, molecular formula and relative molecular weight General description of raw materials Identification of critical steps in process and control Flow diagram of manufacturing process Description and characterization of drug substance Physiochemical data: (Chemical name and structure, Empirical formula, Molecular weight) Physical properties:- Description, Solubility, Rotation, Partition coefficient, Dissociation constant. Analytical Data: Elemental analysis, Mass spectrum, NMR spectra, IR sp...

We are looking for an experienced medicinal chemist with hands-on expertise in small-molecule drug discovery. This role involves driving the design, synthesis, and optimization of chemical compounds from early hit identification through to lead optimization. The ideal candidate will bring strong experimental chemistry capabilities, SAR insight, and cross-functional collaboration skills to advance high-quality drug candidates. Key Responsibilities Design, plan, and execute synthetic routes to support iterative compound design and structure-activity relationship (SAR) studies. Analyze and prioritize screening hits based on potency, selectivity, and chemical tractability. Apply biophysical and ...

Location: Vatva GIDC, Ahmedabad Experience Required: 2 to 3+ Years Qualification: B.E./B.Tech in Chemical Engineering Industry: Textile Dyes (Reactive & Direct Dyes) Job Type: Full-Time ------ About Us: Ashwini Dyechem Industries is a leading manufacturer of high-performance reactive dyes for the textile industry. We are committed to innovation, quality, and sustainability. Join our growing team to contribute to world-class dye manufacturing and cutting-edge lab development. ------ Key Responsibilities: Batch Production: • Supervise and manage daily batch production processes. • Maintain strict process controls and monitor reaction parameters. • Coordinate with the factory team to ensure qua...

Qualification: Masters Relevant Relevant Experience: 8 to 12 years Location: Bengaluru Well versed in handling LC-MS/MS instruments for ADME bioanalysis Responsible for Handling, troubleshooting LC-MS/MS related problems and Bioanalytical execution of all ADME Assays (MDCK, Caco-2, PAMPA, CYP-Inhibition, High-throughput solubility, Plasma stability, Hepatocyte stability, Microsomal stability, Buffer stability, SGF, SIF, etc) Responsible for Maintaining the Bioanalytical project flow for Invitro studies. Handling and Execution of Kinetic solubility, Thermodynamic solubility & Chromatographic Log D studies. Analyzing the MET-ID samples, Report preparation. Training the team members in Bioanaly...

To perform in vitro ADME assays (solubility, metabolic and plasma stability, CYP inhibition, plasma protein binding studies etc.) Design, conduct and report data from in vitro metabolism studies using various cellular and subcellular systems, e.g., microsomes, hepatocytes, recombinant CYPs/UGTs and transfected cells. Perform assays using automated workstations. To design, program and implement study protocols in automated workstations. Ability to integrate metabolism and other supporting ADME data to predict druggability outcomes. To lead a group of 2-5 members and train juniors for the ongoing assays and technologies. Maintain labs & comply with SHE/regulatory guidelines.

About the Role We are seeking a highly motivated and experienced Techno-Commercial professional to join our team and drive the B2B growth of our herbal extract portfolio across global and domestic markets. The ideal candidate will have a strong background in herbal extracts, nutraceuticals, or phytochemicals, with a proven ability to bridge technical expertise and commercial strategy. This is a strategic and client-facing role that involves product presentations, client engagement, technical consultation, solution-building, and driving sales closures across industries like dietary supplements, functional foods, personal care, and pharmaceuticals. --- Key Responsibilities Client Engagement & ...

Sphera is a leading global provider of enterprise software and services that enables companies to manage and optimize their environmental, health, safety and sustainability. Our mission is to create a safer, more sustainable and productive world. Sphera is a portfolio company of Blackstone, a U.S.-based alternative asset investment company that focuses on private equity, technology and innovation, and more. Blackstone businesses succeed through strong partnerships, a personalized approach and a commitment to exceptional performance with uncompromising integrity. Sphera and Blackstone are leaders in the Environmental, Social and Governance (ESG) space. We are guided by our core values of Cust...

Job Overview We are seeking a skilled and detail-oriented Lab Chemist with hands-on experience in the synthesis, testing, and application of dyes and textile chemicals. The ideal candidate will be responsible for conducting lab trials, developing new formulations, improving existing products, and supporting R&D initiatives for reactive, acid, and disperse dyes. Key Responsibilities Conduct laboratory synthesis and standardization of dye batches Perform quality control tests (shade matching, strength, solubility, fastness, etc.) Support scale-up from lab to plant-level production Maintain and improve lab procedures, safety standards, and documentation Coordinate with R&D and production teams ...

Job Description: Job Title: Intern – CMC (Formulation) Duration: 12 Months (1 year) Location: Hyderabad Department: CMC (Formulation) Reporting To: Lead Scientist - CMC (Formulation) Stipend: Paid Qualifications: Master’s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution. Strong academic background in pharmaceutics Basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage. Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing. Excellent communication, organizational, and problem-solving skills. Position Summary: The Formulation R&D Intern...

Job Description: Job Title: Intern – CMC (Formulation) Duration: 12 Months (1 year) Location: Hyderabad Department: CMC (Formulation) Reporting To: Lead Scientist - CMC (Formulation) Stipend: Paid Qualifications: Master’s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution. Strong academic background in pharmaceutics Basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage. Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing. Excellent communication, organizational, and problem-solving skills. Position Summary: The Formulation R&D Intern...

Job Description: Job Title: Intern – CMC (Formulation) Duration: 12 Months (1 year) Location: Hyderabad Department: CMC (Formulation) Reporting To: Lead Scientist - CMC (Formulation) Stipend: Paid Qualifications: Master’s degree in Pharmaceutical Sciences (Pharmaceutics) or related discipline from a reputed institution. Strong academic background in pharmaceutics Basic knowledge of formulation principles and analytical techniques. Familiarity with regulatory guidelines (e.g., ICH, FDA, EMA) is an advantage. Proficient in MS Office (Word, Excel, PowerPoint) and scientific writing. Excellent communication, organizational, and problem-solving skills. Position Summary: The Formulation R&D Intern...

At Ecospice Ingredients Pvt. Ltd., specializing in the production and export of high-quality essential oils, oleoresins, and spice extracts, derived from nature's finest botanicals. Our advanced manufacturing facility, nestled in the heart of Kerala's spice-growing region, is situated within our own spice plantation in Idukki, ensuring freshness, traceability, and quality from farm to formula. With a strong emphasis on purity, innovation, and sustainability, we cater to various industries including food & beverage, pharmaceuticals, cosmetics, perfumery, and wellness. Our cutting-edge extraction techniques preserve the full flavor, aroma, and therapeutic value of each ingredient. Ecospice Ing...

Trending Job Description Responsible to maintain the laboratory as per good laboratory practices, good documentation practices, 21 CFR guidance and meets cGMP Requirement. Responsible to adhere with data integrity policy, ALCOA++ principle during performing any activity inside the company premises. To follow the administrative policies including personal hygiene, HR procedures, environmental and safety regulations within the site premises. To identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness. Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed d...

Job Description Responsible to maintain the laboratory as per good laboratory practices, good documentation practices, 21 CFR guidance and meets cGMP Requirement. Responsible to adhere with data integrity policy, ALCOA++ principle during performing any activity inside the company premises. To follow the administrative policies including personal hygiene, HR procedures, environmental and safety regulations within the site premises. To identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness. Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during ana...

Department: 1. Formulation R&D 2. Analytical R&D Facility: Formulation R&D CentreKey Skills Required: Product Development / Formulation Research development/ Analytical Method Development / Validation / Routine & Stability Sample Analysis / Method ValidationPlease find the JD below: Job Title: Formulation R&D Scientist (Oral Solid Dosage) Job Summary: We are seeking an experienced Formulation R&D Scientist to join our team in developing innovative oral solid dosage (OSD) formulations. The successful candidate will be responsible for designing, developing, and optimizing OSD formulations, ensuring product quality, stability, and performance. This role requires close collaboration with cross-f...

Key Responsibilities: Formulation Development Design & develop new formulations for dietary supplements (tablets, capsules, powders, gummies, liquids, etc.). Optimize existing formulations to improve stability, bioavailability, and efficacy. Evaluate new ingredients, excipients, and delivery systems for nutraceuticals. Product Testing & Analysis Conduct stability studies, compatibility tests, and dissolution studies. Work with analytical teams to ensure quality and consistency in formulations. Regulatory & Compliance Ensure formulations comply with FSSAI, FDA, EFSA, and other international regulations . Prepare technical documents like COAs, MSDS, and formulation dossiers. Research & Innovat...

Job Summary We are seeking a dynamic and detail-oriented professional to join our R&D/F&D team focused on Oral Solid Dosage (OSD) forms, including pellets and tablets. The ideal candidate will be responsible for conducting pre-formulation and formulation development studies, process validation, stability studies, and technology transfer of new pharmaceutical products, while ensuring adherence to ICH guidelines and internal SOPs. Key Responsibilities Literature Survey & Research: Conduct detailed literature reviews to support new product development initiatives. Evaluate reference products, patents, regulatory status, and formulation strategies. Pre-Formulation Studies: Perform physicochemica...

Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor/ HOD-QC/ Head-Quality as and when required. To receive the analysis sample includes In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Initiate the analysis as per work allocation done by supervisor/ HOD-QC of these samples by u...

Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor/ HOD-QC/ Head-Quality as and when required. To receive the analysis sample includes In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Initiate the analysis as per work allocation done by supervisor/ HOD-QC of these samples by u...

Job Description Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor/ HOD-QC/ Head-Quality as and when required. To receive the analysis sample includes In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Initiate the analysis as per work allocation done by supervisor/ HOD-QC of th...

Job Description Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor/ HOD-QC/ Head-Quality as and when required. To receive the analysis sample includes In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Initiate the analysis as per work allocation done by supervisor/ HOD-QC of th...

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Development of parenteral formulations with moderate supervision Conduct pre-formulation studies and define formulation strategy. Able to perform Patent Search, Proof of concept studies for new products. Evaluate/Establish the physicochemical parameters such as Solubility profile, PKa, LogP etc Familiar with Osmolality, Viscosity, Specific gravity, Headspace, Oxygen/light sensitivity study Should able to perform pH stability, Freeze thaw cycling, Material compatibility studies Familiar with In use stability testi...

Be the First to Apply Job Description Responsible to maintain the laboratory as per good laboratory practices, good documentation practices, 21 CFR guidance and meets cGMP Requirement. Responsible to adhere with data integrity policy, ALCOA++ principle during performing any activity inside the company premises. To follow the administrative policies including personal hygiene, HR procedures, environmental and safety regulations within the site premises. To identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness. Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormaliti...