341 Method Development Jobs - Page 14

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 22-08-2025. 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 success of this position. Proven ability to i...

Position: Research Associate / Senior Research Associate position for Mammalian upstream lab R&D Location: Govandi, Mumbai Responsibilities: 1. The candidate should have thorough knowledge of biosimilar upstream process development in mammalian (CHO expression system) 2. Should have experience in handling of CHO based cultures at shake flask level, ambr15 and ambr250 scales 3. Should have experience in process development including media feed screening and physical parameters optimization 4. Should have experience in handling in 5L and 50L with Multiple and Single use disposable upstream equipment 5. Should have experience in troubleshooting in process development 6. Should have experience i...

Job Responsibilities: A) Project Management Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Evaluate methods under consideration by conducting literature survey (incl. regulatory guidelines, pharmacopeia guidelines, publicly available research, etc.) Identify initial cell-lines/ anti-body requirement based on method(s) identified Conduct lab experiments for bio-assay/ immuno-assay development and optimization Conduct lab experiments to qualify the method for reproducibility Prepare/provide inputs for the preparation of necessary documents like Method development report, Method qualification protocol and report. Method validation pr...

Conduct Extractables & Leachable studies Operate LC-MS/MS, GC-MS/MS, UHPLC, GC-FID Method development, validation & data interpretation Ensure GLP, NABL, 21 CFR Part 11 compliance Exp. in PFAS, BPA, Nitrosamines preferred MSc/M.Pharm/Biotech required

Role & responsibilities 1. Development of Analytical methods. 2. Validation of Analytical methods. 3. Preparing analytical method development reports. 4. Literature survey for existing analytical methods. 5. Carry out literature survey by establishing the strategies. 6. Maintenance of FDA department. 7. Coordinating various development activities in FDA laboratory. 8. Maintenance of reference standard, working standards and their standardization. 9. Co-ordinating the activities in Chemical and Instrumentation. 10. Analytical Method Development and handling of Troubleshooting. Preferred candidate profile M.Sc. - Analytical / Organic Chemistry Candidate from Vadodara or nearby location preferr...

Role & Responsibilities: Conducts literature survey for the selected molecule/ drug to support development of analytical method. Conducts routine experiments for the assigned product development project (e.g., analytical method development, de-formulation studies, in-process and stability studies, temperature excursions, cleaning verification, etc.), as per the provided work plan, and assists senior team members in conducting more complex experiments. Maintains online entries in logbooks/ Registers and documentation of experiments conducted. Ensures these are completed and available for reference in the appropriate documentation repository. To prepare and sign off the analytical request form...

Role & Responsibilities: Upkeep the laboratory with respect to cleaning and discipline. To follow the GLP regulations within the laboratory. To perform the method development, in process and stability activity of drug product as per the plan and priority. To record and maintain daily temperature and humidity record of laboratory in logbooks. To follow relevant safety and regulatory norms. To follow all time compliance to company policies and values. To prepare analytical data sheets as per current version of specification and Method of Analysis. To conduct project related analytical activities at Quality Control laboratory. To calibrate the instruments as per the plan or as and when required...

Aragen Life Sciences is seeking an HPLC expert for the position of Analytical Research Scientist to execute method development & validations focused on the API of new chemical entities (NCEs) and generics. The ideal candidate should possess a strong understanding of the fundamentals of analytical chemistry and HPLC combined with expertise in method development and validation based on sound scientific principles.

Principal task: Analytical Method Development by HPLC for all Project. Review the analytical method development data, validation study data and method transfer protocol and reports. Calibration of HPLC system. To maintain GLP/GDP in working environment. Preparation of analytical data and submit for review. Analytical Method Development and Validation. Responsibilities: Calibration of HPLC’s as per SOP and maintenance of HPLC Systems. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. Preparation & Review of analytical method validation protocol and report as per the current regulatory requirement. As per Prot...

Hands on experience in Clinical Research studies

Knowledge on how to develop the LCMS / HPLC suitable method from the GCMS method.Preferable to handling of LC-HRMS instrument and technical knowledge on E & L studies.Method development for GTIs and Nitrosamines by LCMS.Collect the literatures.

1. Routine Analysis 2. Stability Analysis 3. Analytical Method Validation 4. Analytical Method development 5. Documentation-STP and Specification review

Responsibilities: To follow Good Laboratory Practices. Carry out routine analysis & Ensure documents pertaining to day to day analysis. Calibrate instrument used for analysis as per SOP and maintain its record. Method Transfer Activity. Should have experience of handling and calibration of GC, HPLC, KF, UV, Viscometer, Potentiometer, Tintometer, PH Meter etc. Various analyticals methods development and wet analysis along with related documentation. Required Skills Must be excellent in written and spoken English; Net savvy and adept at computer skills. Good in communication. Required Qualification : - B.Sc/M.Sc - Chemistry

Position: Pre-Clinical Designation: Research Associate Job Location: Dholka, Gujarat 1. Study Sample Analysis- Clinical studies 2. Method Development and Method Validation - Preparation of STP And MVP 3. Coordinate with QA & QC department for timely completion of Projects reports 4. Preparation of SOP and method development and method validation documents 5. Maintaining GLP & ensure 100% compliance

Conduct analysis of pharmaceutical products using HPLC. Develop & validate analytical methods. Documentation & Reporting. Calibration & maintenance of analytical instruments. Participate in regulatory inspections and audits, Required Candidate profile Experience of Pharma companies is mandatory. Should be aware of QMS related to QC. It is on the rolls of Cotecna Life Sciences. Share resume on nilesh.kadam@geochem.net.in or call on 9870476784.

Role & responsibilities Handling of Analytical Method validation of Assay and dissolution as per ICH Guidelines. Responsible for the Analysis of Finished products as per STP. Responsible for the Qualification and Maintenance of Working Standards. Responsible for sending of samples to external laboratory and receiving of reports. Maintenance of records / documents for external laboratory services. Dissolution: Carrying out different Media study with compilation of results. Regular Stability Analysis: Well versed with handling of regular Stability samples analysis. Operation and regular maintenance of stability chambers. Documentation: Good knowledge on GLP, GDP, CGMP and maintenance of record...