520 Method Development Jobs - Page 7

Walk In drive for Formulation Analytical Research & Development - Department (FAR&D) - ASQA & ASRD : MSN Laboratories, R&D Center on Friday 26-09-2025. Roles & Responsibilities : ASRD Responsibilities : 1) Execution of Analytical Method validations for drug products for various markets. 2) Execution of DPDM Method validations for drug products. 3) Analytical method transfers to the Quality control labs. 4) Performing the calibrations of the analytical instruments. 5) Preparation & review of Analytical Method validations protocols and reports. 6) Responsible for cGLP, documentation and implementation of departmental quality systems. AQA Responsibilities : 1. Preparation and Review of AQA SOPs...

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. 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 Tentative me...

As an analytical scientist in the Analytical Development department at Azurity Pharmaceuticals, you will be an integral part of the team responsible for developing new analytical methods for novel dosage forms to ensure product quality. Key Responsibilities: - Develop analytical methods primarily for sterile and oral dosage forms. - Prepare method development reports, validation protocols, test methods, and execute Analytical ATR. - Perform routine analytical testing for assigned projects and communicate findings to the formulation development team. - Calibrate equipment, qualify working standards, and maintain standards based on storage conditions. - Conduct forced degradation studies, iden...

As a Site Transfer and ANDA Specications Specialist at our company, you will play a critical role in creating, revising, and reviewing specifications and methods for site transfers and ANDAs. Your responsibilities will include: - Having knowledge of method validation protocols and being able to create, revise, and review validation reports for drug substance, excipients, and drug products. - Initiating change controls as necessary for various aspects including method and specification revisions, stability protocols, batch analysis, reference standards, characterization of impurities, justification of specifications, facility templates, stability summary reports, 5313 reports, QOS, and stabil...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. - Developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according to ICH and regulatory guidelines....

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a p...

* Perform pre-formulation studies , R&D trials and support scale-up activities * Conduct R&D trails for oral solid dosage forms *Develop and optimize formulation to meet regulatory and quality reequipments * Document and analyze trial data to improve formulation *Dissolution, Method development , Method Validation

Analysis of routine samples (product development batches, stability study samples, raw materials etc.). Operation and Calibration of analytical instruments/equipment s. Analytical activities related to Quality control department. Qualification of working standards. Documentation of analytical activities as per good documentation practices. Work in laboratory as per good laboratory practices. To use PPEs and follow safe practices in lab. Any other task assigned by management. Sampling of raw materials from pilot plant dispensing area. Analysis of samples in quality control laboratory. Operation and Calibration of instruments in quality control laboratory

Multiple requirements as Analyst for HPLC, GC and ICP at middle and senior level. Experience from public testing lab will be an added advantage. Preference will be given to immediate joiners or who are ready to join in short notice period. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in or any more information call on 9870476784

Job Title: Analyst / Senior Analyst IVRT / IVPT Company: Energon Labs Location: Hyderabad Employment Type: Full Time, Permanent Role Overview We are looking for skilled Analysts / Senior Analysts with expertise in IVRT (In Vitro Release Testing) and IVPT (In Vitro Permeation Testing) . The role involves performing studies on topical and transdermal products, conducting diffusion experiments, and developing analytical methods to support pharmaceutical R&D. Key Responsibilities Conduct IVRT studies for topical and transdermal formulations. Perform IVPT studies using human/animal skin with Franz diffusion cells. Develop and validate methods for topical dosage forms, including content/assay and ...

Job Title: AQA Quality Assurance (LCMS, GCMS, ICPMS) Company: Energon Labs Location: Hyderabad Experience Required: 2 - 6 years Employment Type: Full Time, Permanent Role Overview We are seeking experienced professionals in Analytical Quality Assurance (AQA) to review and ensure compliance in analytical data generated through LCMS, GCMS, and ICPMS techniques. The role requires a keen eye for detail, strong knowledge of analytical methods, and the ability to uphold the highest quality standards. Key Responsibilities Review analytical data for LCMS, GCMS, and ICPMS techniques. Conduct electronic audit trail reviews for analytical instruments and ensure compliance. Review Analytical Method Vali...

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) Walk-in interview 22-Sept to 26-Sept 9.30am to 5pm on 27-Sept-25(Saturday) from 9.30am to 3pm

Role & responsibilities Preferred candidate profile

Perform AMD & AMV for API dosage forms, handle HPLC/GC, develop stability-indicating methods (ICH, USP, EP, JP), impurity profiling, forced degradation, residual solvent analysis, method transfer, troubleshooting & compliance with GLP/GMP.

Role Overview: You will be working as an Executive - QC in the Small Molecule Bioanalytical Research Laboratory at Syngene International Ltd. in Bangalore, India. Your main responsibility will be to review data for BA/BE studies in the laboratory, including checking method development, validation, and sample analysis data. You will report to the Head / Group Leader of the Small Molecule Bioanalytical Laboratory. Key Responsibilities: - Perform data checks (QC) for method development, validation, and study sample analysis. - Review STPs, Protocols, validation, and bioanalytical reports. - Ensure necessary documents and records are updated and ready for audits (Sponsor / Regulatory). - Handle ...

Role Overview: You will be responsible for ensuring the timely and compliant review of CMC documentation, Method Development/Validation Protocols & Reports, Stability Protocols & Reports, Instrument/Equipment Qualification records, and BMR. You will also be involved in compiling high-quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various sites, liaising with third party contract manufacturers, and recommending actions for continuous improvement in product quality. Additionally, you will participate in Quality Management Systems, Performance Management, Training, and provide miscellaneous support as needed. Key Responsibilities: - Review CM...

Home The University Job Opportunities and Working At Swansea Current Vacancies Research Officer in Antihydrogen Physics Back to list Research Officer in Antihydrogen Physics Related pages Current Vacancies Benefits & Rewards Equality Diversity & Inclusion Information for Applicants Information for for colleagues from around the world Our reward and benefits, and ways of working enable those who join us to have enriching careers, matched by an excellent work-life balance, About The Role The group is a leading member of the ALPHA collaboration with responsibility for positrons, antihydrogen synthesis, laser-spectroscopy and frequency metrology Recent research highlights include the first laser...

Developing and validating analytical methods for new and existing products Analyzing samples using various analytical techniques such as HPLC, GC, and LC-MS. Ensuring compliance with regulatory guidelines and quality standards. Accurately and timely documenting and reporting analytical findings. Collaborating with R&D and PD chemists to support product development. Troubleshooting and optimizing analytical methods and instrumentation. Maintaining lab instruments and ensuring they are in good working condition. Providing technical guidance and training to junior team members. Keeping the working area tidy and near regularly. Reporting: Head of R&D

As an ARD Chemist / Scientist at the Udaipur location, you will be a key member of the ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support Synthesis R&D and quality operations. - Developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples. - Developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. - Performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry. - Ensuring that all analytical instruments are maintained in optimal working condition through regula...

Job Description: As a qualified candidate for this role, you should hold a Master's degree in Analytical Chemistry. Additionally, you should have 6-9 years of experience in method development and validation. It is important that you are willing to work in shifts. Key Responsibilities: - Develop and validate analytical methods for various projects. - Perform analytical testing and provide accurate results. - Collaborate with cross-functional teams to ensure project success. - Maintain laboratory equipment and ensure proper calibration. Qualifications Required: - Master's degree in Analytical Chemistry. - 6-9 years of experience in method development and validation. - Willingness to work in sh...

Description We are seeking a skilled QA & QC Chemist to join our team in India. The ideal candidate will be responsible for ensuring the quality and safety of our chemical products through rigorous testing and analysis. This role is critical in maintaining our high standards and compliance with industry regulations. Responsibilities Develop and implement quality control procedures for testing and analyzing raw materials, intermediates, and finished products. Conduct routine laboratory tests and analyses to ensure compliance with quality standards. Document and report on the findings of tests and analyses, maintaining accurate records of results. Collaborate with production and R&D teams to a...

Analytical chemist Shift - 9 am to 6 pm Package - 25 k to 40 k(3 year experience) location- patiala Skills- pharma Wtsapp me resume at 8295842337- Mr. Bansal

Role & responsibilities Literature Survey for the assigned project. Analytical method development such as Assay, Dissolution, Related Substances method by HPLC. Analytical method validation of Assay, Dissolution, Related Substances method by HPLC as per ICH guideline by HPLC. 4. Analysis of Initial and stability samples. 5. Carry out basic trouble shooting for instrument related issues, whenever required. Email id- namita.raul@ashishlifescience.com Contact- 8657894640

Role & responsibilities 1.Stability Studies Management: Planning and management stability studies, Comparative Stability and Forced Degradation (FDS) Studies, Reference product age related studies of all the projects. Compilation of stability data, interpretation, and data trending. To review the data, related DRS and LNBs etc. 2. Drafting / review / approval of operational SOP, LP, SLP and Stability Protocols, Summary Sheets, Reports as required. 3. Planning and management of the IRS: Planning and management for establishment of internal reference standards. Management of IRS stability studies, issuance, compilation and trending the retrospective data of the established internal standards. ...

Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activities in a saf...