518 Method Development Jobs - Page 3

Chiral Biosciences is looking for Research Scientist Organic Synthesis to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Role & responsibilities 1. Proper maintenance of LC-MS/MS/ HPLC/ UPLC and their records of calibration. 2. To develop and validate Bio-analytical methods. 3. To process and analyse biological samples for drug/metabolite concentrations 4. To compile raw data and record laboratory note books/logbooks 5. To maintain equipment logbooks 6. To assist Lab Manager in data analysis and compilation of reports 7. Proper operation and routine maintenance of laboratory equipment in Bio analytical department 8. Responsible for laboratory instruments like PH meter, analytical balance, micro pipettes, etc. 9. Recording and reviewing of all raw data, method SOPs method validation reports and bio analytical r...

Experience in Operation and calibration of LCMS /GC Method development and validation of Genotoxic impurities/ nitroso amine impurities/NDSRIs in pharmaceutical products/ substances by LC-MS/MS. Development of MS compatible methods for the HPLC RS methods for the identification of unknown peaks by LC-MS Development of MS compatible methods for the identification of degradation impurities and unknown impurities

An ADL (Analytical Development Laboratory) role in API job responsibilities includes developing and validating analytical methods for raw materials, intermediates, and finished APIs, performing routine

SRL Pharma R&D Centre urgently required below mentioned profiles with Exp. 2 - 6 Yrs. DQA - Development Quality Assurance - 2 Post Analytical R&D - 4 Post API R&D - 4 Post Please share profile on hr@shivalikrasayan.com, uday@shivalikrasayan.com Required Candidate profile Pharma R&D experience must in DQA, Analytical & API R&D (M.Sc.) Preparation of Pharmaceutical Development report Ready to relocate Bhiwadi, Rajasthan Ready to join Immediately Prefer Team Player Perks and benefits Best of Industries Salary based on Experience

Roles and Responsibilities These statements reflect the general description of the position and are not intended to be an all inclusive list of tasks to which employee may be assigned A. Prepare Sample analysis report, Incurred sample reanalysis report & Method validation report in compliance with standard operating procedure and respective regulatory requirements such as USFDA, EMA, TGA, MCC, CANADA, NMPA, etc.. B. Ensure additional summary/module 2 (as applicable) is prepared as per respective regulatory and sponsor requirements. C. Handle Sponsors or regulatory queries on lab reports. D. To ensure that lab reports are released within their timelines. E. Maintain documents and databases fo...

You will be responsible for leading the characterization of peptides and small molecules using Liquid Chromatography and High-resolution mass spectrometry (LC-HRMS, LC-MS/MS) to determine structural elucidation and impurities profiling. As a Team Lead, you will manage a team focused on Peptide / Protein characterization through HRMS. Your duties will include method development, impurity profiling of Peptides/Proteins, and Impurities characterization using HRMS. Additionally, you will utilize spectroscopy (UV-Visible, Circular Dichroism, Spectrofluorometer), Capillary Electrophoresis, and analytical method development for characterization purposes. - Handling LC-HRMS for Characterization of P...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

Description We are seeking a skilled Lab QC Chemist to join our team in India. The ideal candidate will be responsible for ensuring the quality and safety of our products through rigorous testing and analysis in a laboratory setting. Responsibilities Conduct quality control testing of raw materials, in-process samples, and finished products. Develop and validate analytical methods to ensure compliance with regulatory standards. Maintain and calibrate laboratory instruments and equipment. Document all testing procedures and results accurately and promptly. Identify and troubleshoot any issues arising during the testing process. Ensure compliance with safety and quality regulations in the labo...

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. (Only Males) Experience : 2 - 6 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of...

You will be responsible for following standard practices cGLP during lab experiments, cleaning verification method development, API method evaluation and verification, API solubility study assessment, working standard qualification, method development and verification of drug product formulation, ARF release of raw material and packaging material, preparation of test procedures for routine development analysis, column management, TOC sample analysis, ensuring in-house compliance system, maintaining hygienic conditions in the respective department, and following GxP (GMP, GDP, GLP) for all processes. Key Responsibilities: - Follow cGLP during lab experiments - Develop and verify cleaning veri...

Job Description: You should have exposure to Method Development, Method Validation, and Method Transfer as per the requirement of ICH. You will be responsible for preparing protocols and executing planning for activities as per the product requirement. Key Responsibilities: - Develop methods for analysis - Validate methods according to ICH guidelines - Transfer methods to different locations as necessary Qualifications Required: - Experience in Method Development, Validation, and Transfer - Knowledge of ICH guidelines,

Role & responsibilities Role Overview You will ensure that all natural food colour raw materials, in-process samples, and finished goods meet quality and regulatory standards. The role involves routine testing, documentation, and compliance support to maintain consistent product quality. Key Responsibilities Conduct routine analysis of raw materials, intermediates, and finished natural colour products. Test and validate key parameters (colour value, pH, solubility, stability, microbiological safety, heavy metals, etc.). Generate and review Certificates of Analysis (COA) for customer dispatches. Maintain and calibrate laboratory instruments (HPLC, UV-Vis spectrophotometer, TLC, GC-MS, etc.). ...

Job Title: Executive – Analytical Development Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Job Description To work as per cGMP and ensure its...

Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices. Responsible to perform the Analytical method validation, method verification and method transfer activities.

Develop analytical methods for biochemistry samples using GC-MS, LC-MS, and other relevant techniques. method validation, optimization, and transfer to ensure accuracy and reliability of results. data analysis, and reporting in accordance .

As a Biology expert, you will be responsible for the following key responsibilities: - Expertise in handling HPLC and LCMS, including troubleshooting techniques. - Proficiency in different extraction procedures and independent handling of bioanalysis for various matrices in PK and ADME studies. - Good understanding of various column chemistry and its application in method development. - Ensuring data integrity and maintaining good documentation practices, including recording data in LNB and completing studies as required. - Operating and maintaining laboratory equipment. - Ensuring all instruments are maintained in a calibrated status. - Managing consumables and chemicals necessary for the s...

Role Overview: As an Analytical Development Scientist, you will be responsible for departmental operations and project delivery. You will work closely with the project lead and Analytical Development Manager to ensure efficient use of time, maintain laboratory areas, provide training and troubleshooting support, and engage in compliance and improvement projects. Your role will also involve leading aspects of projects, planning and carrying out work to ensure effective project progression, supporting method development, and providing project support for analytical development. Additionally, you will be responsible for ensuring timely close out of deviations, upholding cGMP principles and ESH ...

The Manager of Analytical Development will be responsible for developing and implementing analytical methods, quality control, conducting laboratory skills, method development, and research and development (R&D) activities.. No of Vacancies 1. Education Bachelors or Masters degree in Pharmacy, Chemistry, or related field.

Job Description: Knowledge of calibration and operation of LCMS/GC systems with Empower software. Sound knowledge of analytical method development and validation. Handling final compilation of raw data and chromatographic data complying with GLP requirements. Preparing general lab SOPs and instrument SOPs.

We are looking for a skilled HR professional with strong expertise in Payroll Management, HR Analytics, and Dashboard Reporting, coupled with hands-on experience in Darwinbox HR Core Modules. The ideal candidate will drive operational excellence across payroll processes, ensure compliance, and enable data-driven decision-making through analytics and reporting.

JD: 1) Working as per company / management policy & reporting to Quality Control Head. 2) To conduct analysis and testing of Raw Material, Packing Material, In-Process sample, Finished goods, Stability samples etc. with the help of analytical instruments and techniques. 3) To calibrate / verifies analytical instruments i.e. ICP-OES, Ion Chromatography etc..and balances. 4) To trouble shoot analytical instruments. 5) Preparation and standardization of Volumetric Solution. 6) Preparation and maintenance of records for stock / reagents. 7) Analysis of samples for qualitative and quantitative test parameters as per specification. 8) To maintain record of analysis and supporting logbooks as per G...

Walk In drive for Formulation Analytical Research & Development - department (FAR&D) - Quality Inn Ramachandra, Ward No- 58, 31-41/10/1, Duvvada, Revenue, Visakhapatnam, Andhra Pradesh on 25.10.2025 (Saturday ) Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Roles & Responsibilities : 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,...

Dear All, We are looking for an experienced professional to lead Analytical Method Validation activities for Finished Dosage Formulations (OSD) . The ideal candidate should have extensive experience in analytical development, method validation, and regulatory compliance for both domestic and international markets. Experience: 11-13 Years Location: Hyderabad(Dulapally) Key Responsibilities: Plan, design, and execute Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) activities for formulations as per regulatory guidelines (ICH, USP, EP, WHO, etc.). Review and approve Validation Protocols, Reports, Method Development Reports, and Specifications. Ensure method robustness, a...