70 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 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...

Be the First to Apply Job Description Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference st...

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...

Job Description Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity stan...

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 testing, Preservative effectiveness testing concepts Perform product developability risk assessments and Drafts Scientific protocols and reports. Preparation of Stability protocols and st...

: Research Scientist1 DMPK Applications are invited for the post of Research Scientist1 DMPK at the Foundation for Neglected Disease Research at Bengaluru. Foundation for Neglected Disease Research (FNDR) is a unique not-for-profit R&D organization dedicated to developing novel therapeutics, diagnostics, and devices for diseases with a high socio-economic impact. Roles And Responsibilities The key responsibility of the candidate will be to perform and analyze in vitro and in vivo DMPK studies to support drug discovery and development projects. The candidate will be involved in planning, designing, and set-up of DMPK experiments, handling instruments, maintaining the laboratory, and preparing...

To perform calibration of the analytical instruments as per calibration schedule Follow the standard practices cGLP during lab experiments Cleaning verification method development and validation API method evaluation and verification API solubility study assessment Working standard qualification Method Development for drug product formulation Routine analysis of development samples and lab stability samples Method verification of different analytical methods Reporting of analytical data and submit for review and release ARF release of raw material and packaging material Preparation of test procedures for routine development analysis Follow in-house compliance system Maintain hygienic conditi...

To perform calibration of the analytical instruments as per calibration schedule Follow the standard practices cGLP during lab experiments Cleaning verification method development and validation API method evaluation and verification API solubility study assessment Working standard qualification Method Development for drug product formulation Routine analysis of development samples and lab stability samples Method verification of different analytical methods Reporting of analytical data and submit for review and release ARF release of raw material and packaging material Preparation of test procedures for routine development analysis Follow in-house compliance system Maintain hygienic conditi...

Job Description To perform calibration of the analytical instruments as per calibration schedule Follow the standard practices cGLP during lab experiments Cleaning verification method development and validation API method evaluation and verification API solubility study assessment Working standard qualification Method Development for drug product formulation Routine analysis of development samples and lab stability samples Method verification of different analytical methods Reporting of analytical data and submit for review and release ARF release of raw material and packaging material Preparation of test procedures for routine development analysis Follow in-house compliance system Maintain ...

Be the First to Apply Job Description To perform calibration of the analytical instruments as per calibration schedule Follow the standard practices cGLP during lab experiments Cleaning verification method development and validation API method evaluation and verification API solubility study assessment Working standard qualification Method Development for drug product formulation Routine analysis of development samples and lab stability samples Method verification of different analytical methods Reporting of analytical data and submit for review and release ARF release of raw material and packaging material Preparation of test procedures for routine development analysis Follow in-house compl...

Title: Senior Officer Custom Field 2: 2727 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Analysis of raw material, Drug substance (API), Intermediates, by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer Instruments. Analytical method development for raw material and finished products (drug products) by HPLC, GC, GC-MS, LC-MS, NMR, FT-NIR, UV-Visible Spectrophotometer, Dissolution Instruments. Preparation and maintenance of volumetric solutions, buffers, etc Calibration of laboratory Instrument like UV-Visible Spectrophotometer, Balances, pH meter, KF Titrator, etc., ...