945 Method Validation Jobs - Page 8

You will be working as a part of a team in Method Validation Research Laboratory, where your key responsibilities will include: - Setting up Laboratory Equipment and conducting tests and experiments. - Recording the data accurately. - Presenting results to senior research staff. - Keeping up to date with relevant scientific and technical developments. - Performing Synthesis Reactions to contribute to the research projects. The ideal candidate for this role should have the following qualifications and experience: - Qualification: M.Sc. Organic Chemistry/M.Sc. Chemistry. - Experience: 1 to 4 Years in Pharma Industry. Please note that the company, Global Calcium, is one of the leading API manuf...

The successful candidate will be responsible for designing, developing, and optimizing OSD formulations, ensuring product quality, stability, and performance. Interested candidates please sent your resumes to email id: jones.naveen@insta-pill.com Food allowance Health insurance Office cab/shuttle Provident fund

Position: ADL Executive Location: Torrent Research Centre - Gandhinagar, Gujarat Experience required: 3 to 8 Years in ADL Method Development for Formulation/API Qualification: M.Sc./M.Pharm Required Experience HPLC/GC method development having exposure to regulated, Semi Regulated & India markets including: Complex generic, F2F, Topical & Dermaceuticals, Peptides, Oncology, OSD Job Description To develop analytical method for Assay, Related Impurity (Degradation Product), Content uniformity, Dissolution and other related tests Dissolution testing and evaluation. Analyzing formulation and raw materials Performing pre-formulation analysis To analyze formulation trials To analyze stability samp...

As a Technical Manager LAB, you will be responsible for the laboratory's technical requirements, activities, and implementation under the guidance of the Quality Manager. Your key responsibilities will include: - Selection, verification, approval, and commissioning of test methods. - Allotment of samples to Chemists for analysis. - Management of smooth working of equipment and facilities, ensuring availability of laboratory consumables, proper calibration of instruments, and maintenance of environmental conditions. - Design and implementation of the QC programme to assure quality results through various checks and comparison with proficiency testing and inter-intra laboratory programs. - Exa...

Job Description: As a member of the team at Amneal, your role will involve core analytical method development and CMC activities for Inhalation dosage forms. You will be responsible for performing analytical activities related to development, scale-up support, method validation, method transfer, release, stability, drug product characterization, E&L Study, In-vitro study, and routine analysis of inhalation dosage forms. Your tasks will include conducting tests such as assay, related compound, APSD, DDU, and particulate matter analysis for inhalation dosage forms. Qualifications: - M. Pharm / M. Sc. / B. Pharm About Us: Amneal is committed to being an equal opportunity employer, where we valu...

1 + Years of experience in RM, GLP, Micro, FP & Stability (HPLC User must) Formulation Job Location: Daman (Interview : Ahmedabad) Experience: 1 to 9 years in Formulation Qualification: M.Sc./B.Pharm/M. Pharm Required Candidate profile Experience in Section LCMS / PSD / HPLC / GC /Method Validation Pharma API. Job Location: Dahej (Interview : Ahmedabad) Experience: 2 to 7 years in API Qualification: M.Sc./B.Pharm/M. Pharm

Design, plan, perform, interpret and report the analytical results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within global ARD. Expertise in analytical method development, method validation as well as technical and strategic background. Manage technical lab/plant activities. Execute the analytical experiments in line with TRD vision. Ensure full portfolio support in line with GDD, NTO and NIBR plans. Maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned. About the Role Major accountabilities Provide analytical and technical support to PHAD/project t...

Perform analytical testing of raw materials, in-process, and finished products using HPLC. Prepare reagents, calibrate instruments, document data, troubleshoot issues, ensure compliance with GMP, and support method validation and investigations. HPLC operation and troubleshooting Education - Bachelor's or Master degree in Chemistry

Collate/prepare and file dossiers in a timely and accurate manner for Formulations and API products to get licenses from various targeted markets (Emerging Markets/ROW). Review and regulatory impact analysis of the change control, communication with customer for notification and approval as applicable. Review and regulatory impact analysis of the changes notified by the vendors as per current regulatory requirements (country specific), as desired. Evaluate any changes proposed post-approval. Prepare and file necessary amendments / supplements / annual reports as applicable to ensure regulatory compliance (Post-approval Life Cycle Management). Prepare the checklist for documentation for regul...

Summary Design, plan, perform, interpret and report the analytical results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within global ARD. Expertise in analytical method development, method validation as well as technical and strategic background. Manage technical lab/plant activities. Execute the analytical experiments in line with TRD vision. Ensure full portfolio support in line with GDD, NTO and NIBR plans. Maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned. About The Role Major accountabilities: Provide analytical and technical support to PHAD/...

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 ...

As an Analyst in the Instrument Lab specializing in LCMS at our company in Mumbai, your responsibilities and authorities will include: - Complying with the laboratory's Quality Policy, Quality Objectives, and Quality Management System (QMS) procedures. - Performing sample preparation, instrument setup, and testing using LC-MS (Liquid ChromatographyMass Spectrometry) as per approved methods and SOPs. - Ensuring that all analyses are carried out accurately, efficiently, and within the specified turnaround time to meet customer and regulatory requirements. - Calibrating, operating, and maintaining the LC-MS and associated instruments (HPLC, balances, pipettes, etc.) as per the preventive mainte...

Summary Design, plan, perform, interpret and report the analytical results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within global ARD. Expertise in analytical method development, method validation as well as technical and strategic background. Manage technical lab/plant activities. Execute the analytical experiments in line with TRD vision. Ensure full portfolio support in line with GDD, NTO and NIBR plans. Maintain and qualify equipment/infrastructure and manage operational aspects in lab or plant as assigned. About The Role Major accountabilities: Provide analytical and technical support to PHAD/...

Responsible for analytical method development, validation & transfer, ensuring cGMP & regulatory compliance. Supports R&D projects, stability studies, and dossier preparation for global submissions. Required Candidate profile M.Pharm or M.Sc with 10–15 years in AR&D for formulations. Hands-on with HPLC/GC, stability studies & regulatory documentation.

Coordinate with ADL Manager and CSL Group Leader for analysis-related work. Ensure availability of columns, reagents, and consumables through coordination with Purchase & R&D Admin. Support analytical method transfer and equipment upkeep in API Co. Required Candidate profile M.Sc.(Chemistry) with 2 to 3 years experience analytical chemistry and method validation. Knowledge to Develop and validate analytical methods for raw materials, intermediates, APIs

Experience of Analytical tools in chemicals or Intermediates Experience of Wet Lab analysis is also required important IT tools: Scifinder, Chemdraw, and good computer proficiency is needed

Every day, we get opportunities to make a positive impact on our colleagues, partners, customers and society. Together, we re pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to act on initiative, we challenge conventional thinking to develop world-leading technologies that inspire progress in vital areas, including energy, food, water and shipping. As we push forward, the innovative, open spirit that fuels our 140-year-old start-up culture and rapid growth also drives our personal growth. So, as we shape a more resourceful, less wasteful world, we build our careers too.

Roles and Responsibilities Develop new APIs through organic synthesis, method development, and optimization. Conduct literature reviews to stay updated on latest research trends and technologies. Ensure compliance with GMP guidelines during API manufacturing processes. Collaborate with cross-functional teams for product development, scale-up, and commercialization. Perform impurity analysis using techniques like NMR, DSC, etc. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Ph.D/Doctorate in Chemical Sciences from a recognized university. Strong expertise in areas such as API synthesis, organic chemistry, method development/validation/transfer/methodology. 9-14 years of exp...

calibration &method validation by using LCMSMS/GCMSMS in Food and water samples. Sample preparation for pesticides residue and antibiotics in food samples. Testing of Pesticides Residue, Antibiotics, PAH&PCBs, ETO,PFAS, PA/TA

Job Title: Senior Microbiology Trainer Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced Microbiology Trainer with over 10 years of professional experience in academic, industrial, or laboratory microbiology. The trainer will design, deliver, and evaluate microbiology training programs for students, fresh graduates, and professionals working in pharmaceutical, food, and life sciences industries. Key Responsibilities: Conduct hands-on and theoretical training sessions on Microbiology fundamentals , Industrial & Pharmaceutical Microbiology , and Quality Control techniques . Train participants on GMP/GLP , sterility testing , environmental monitoring , microb...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories Private Limited MSN House, D.No: 2-91/10 & 11, White Fields,Kondapur, Hyderabad on Sunday 16-11-2025 Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the suc...

Role & responsibilities Collect samples for analysis from custodian. Processing of sample by using various sample extraction technique (to determine the concentration of analyte). Perform analysis via LCMS. Follow GXP. Sample extraction process using LLE, SPE, PPT. Stability issue handling, derivatization, etc. approach. Receive controlled forms for various activities. Document all linked activities and forms as per SOP. To check documents done by Jr. Analyst/ Fresher. Method development skills Trouble shooting of method Excel and MS Word.

Regular Batch Analysis by using GCMS. Experience in Method Development & Method Validations Experience in GTI & NDSRI by GCMS

The successful candidate will be responsible for designing, developing, and optimizing OSD formulations, ensuring product quality, stability, and performance. Interested candidates please sent your resumes to email id: jones.naveen@insta-pill.com Food allowance Health insurance Office cab/shuttle Provident fund

Analytical Techniques: Versatile handling of HPLC, GC, PSD, UV, and FT-IR analysis, with hands-on experience in troubleshooting, calibration, and method validation. Statistical Analysis: Familiar with statistical concepts relevant to analytical method validation. Software: Skilled in MS Word and Excel for technical documentation, data analysis ( Excel-based statistical functions), and reporting. Regulatory Compliance: Experienced in managing USFDA and other international regulatory audits. Cross-Functional Collaboration: Strong ability to work effectively with QA, QC, and R&D teams to ensure method robustness and regulatory compliance. Must be having experience in API Designation - Executive...