455 Lcms Jobs

Role & responsibilities Manager technical is the In-charge of Analytical Division. He/She shall report to the SBU-head about all the activities in the Analytical Division. He/She shall look after all the operations of the Division under the guidance/ supervision of SBU-Head. He/She shall be responsible for the standardization and validation of the test methods. He/She shall be responsible for ensuring the availability of the reference material / working reference standard. He/She shall be responsible for assigning the jobs to the analyst as per their calibre. He/She shall be responsible for checking the calculation part and reporting of the results before sending for authorized signatory. He...

Position: Analyst Quality Control LCMS (Liquid ChromatographyMass Spectrometry) Qualification: M.Sc. in Analytical Chemistry or related field Experience: 1 to 2 years Key Responsibilities: Perform LCMS analysis for routine, stability, and validation samples. Support method development and transfer activities. Maintain instrument calibration logs and documentation. Ensure cGMP, data integrity, and safety compliance. Work in shifts as per laboratory requirements. Skills Required: Hands-on experience in LCMS operation. Attention to detail and accuracy in documentation. Basic understanding of analytical method validation.

Position: Manager Quality Control -LCMS (Liquid ChromatographyMass Spectrometry) Qualification: M.Sc. in Analytical Chemistry or related field Experience: 10-15 years Key Responsibilities: Lead installation and qualification of LCMS instruments. Manage method development, validation, and transfer activities. Supervise routine and non-routine sample analysis using LCMS. Ensure data integrity, cGMP compliance, and documentation accuracy. Review analytical reports, protocols, and SOPs. Coordinate with QA, R&D, and Production for analytical support. Train and guide the team; manage activities across shifts. Participate in internal and external audits and ensure timely closure of observations. Sk...

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department Masters degree level in Chemistry,M pharmacy & B pharmacy 2023,24,25 passed outs. 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Bio-analytical: Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the con...

Regular Batch Analysis by using LCMS. Preparation and analysis of method validation, method transfer, method verification and method development protocols and reports. Experience in GTI & NDSRI by LCMS

Developing analytical methods and validating for NCEs and generic compounds by HPLC-UV, GC, LC-MSMS, ICP-MS Dose verification analysis in preclinical dose formulation samples by HPLC-UV, GC, LC-MSMS Generating COA for IND’s Calibration of lab equipment’s like HPLC, pH meter, balances, and pipettes Safe maintenance of raw data Work experience in GLP/GMP lab Preparation of study protocols and SOP’s Maintaining the lab as per GLP

As an Assistant General Manager in Research & Development at an Indian Pharmaceutical MNC based in Thane, you will play a crucial role in leading the Analytical Method Validation team. Your responsibilities will include overseeing validation activities, ensuring regulatory compliance, driving quality and efficiency, and fostering collaboration with R&D, Regulatory, and Plant QA/QC teams. Key Responsibilities: - Provide leadership for analytical method validation (AMV) across multiple dosage forms. - Oversee RM and PM characterization in compliance with regulatory requirements. - Plan and manage validation projects adhering to international regulatory guidelines. - Act as an SME for analytica...

Role Overview Position Title: Team Leader - Process R&D Role Band : L1 Location : Hyderabad Purpose: Lead the design, development, and scale-up of safe, robust, and cost-efficient chemical processes that meet client specifications for quality, yield, and timelines. Objective: Ensure on-time delivery with scientific rigor, data-driven decision-making, and measurable value addition across route selection, optimization, and tech transfer. Minimum Requirements Education: PhD in Organic Chemistry with 10 + years of experience (Mandatory) Business/Domain Understanding: Strong grasp of CDMO workflows, client expectations, IP awareness, and drug discovery/development interfaces (non-GMP to GMP hando...

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 Ingrevia Limited JubilantIngrevia...

Responsible for synthesis, purification, and identification of organic compounds. Perform reactions, analyze using HPLC/NMR, maintain documentation, ensure lab safety, and support R&D through literature review and process optimization.

Role Overview: As a General Manager - R&D at Gujarat Fluorochemicals Limited, you will be entrusted with the responsibility of leading the Research & Development team. Your primary focus will be on conducting literature surveys, identifying viable processes for fluoro-specialty molecules, developing industrial processes, innovating new products, preparing various reports, and scaling up processes from lab to commercial level. You will also lead a team of scientists and chemists, ensuring new product development and continuous improvement of existing products. Key Responsibilities: - Conduct literature survey to identify viable processes for fluoro-specialty molecules - Develop and standardiz...

As a Quality Assurance & Analytical Chemist at FMC, you will be part of a team dedicated to providing innovative solutions for agriculture and the planet. Your role will involve utilizing your knowledge and experience to provide daily analysis support, develop, validate, and apply modern analytical technologies, and ensure quality standards are met at the Toller site. You will be expected to work collaboratively with the team, adapt to changes, and meet project quality and timing needs. **Key Responsibilities:** - Know, understand, and practice all aspects of laboratory safety and industrial hygiene protocols. - Develop, validate, and implement methods for qualitative and quantitative analys...

As a Quality Assurance & Analytical Chemist at FMC, you will play a crucial role in providing daily analysis support by developing, validating, and applying modern analytical technologies for the development and commercialization of agricultural products. Your responsibilities will include: - Knowing, understanding, and practicing all aspects of laboratory safety and industrial hygiene protocols. - Developing, validating, and implementing methods for qualitative and quantitative analysis to meet business needs. - Conducting routine and non-routine analysis of process technical data to ensure project quality and timing needs are met. - Collecting data, generating summaries, and reports. - Sup...

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Saturday 01-10-2025. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,LCMS,GC,GCMS,PXRD High performance liquid chromatography HPLC,GC,GCMS,PXRD HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guidelines...

We Are Hiring Walk-In Drive for Quality Control (QC) Professionals! Hetero is conducting a walk-in recruitment drive for our Quality Control Department. If you are passionate about pharmaceutical quality systems and ready to build a strong career, we would love to meet you. Interview Date: 02nd November 2025 (Sunday) Time: 9:00 a.m. to 3:00 p.m. Venue: VR ASHOKA GRAND Allwyn X Road, Gachibowli - Miyapur Rd, Towards Kondapur, Hyderabad, Telangana 500049 Work Location: Jadcherla Open Position: Jr. Officer / Officer / Executive / Sr. Executive Department: Quality Control Qualification: B.Sc / B.Pharm / M.Sc / M.Pharm Experience: 19 Years Skill Areas: HPLC, GC, RM, PM, IP/FP, LIMS, Stability, Sa...

Position - Group Leader API – Analytical Development Qualification - PhD in Analytical Chemistry Additional Qualification - Research experience from Analytical R&D center of reputed API company Experience - 10-15 Years in APIs Position Objective & Responsibilities Position Summary: The Group Leader – ARD will be responsible for leading the analytical research and development activities for new and existing API products. The role involves method development, validation, impurity profiling, stability studies, and ensuring compliance with regulatory requirements (USFDA, EMA, MHRA, etc.). The position demands strong technical expertise, leadership skills, and experience in managing a team of ana...

Role & responsibilities To perform Physico Chemical Parameters/Method development/Method Validation/Residue Studies/Stability studies /E-fate Studies. Strong knowledge, Handling and operations in analytical techniques, including HPLC, GC, FTIR, UV-VIS, LC-MS/MS and GC-MS/MS spectroscopy, etc. Preferable handling in LC-MS/MS and GC-MS/MS instruments. Develop and validate analytical methods for the analysis of various compounds using a variety of analytical instruments and along with troubleshooting. Understanding of regulatory requirements (OECD/EC/OPPTS/CIPAC/ASTM/SANTE/SANCO/EMA/ICH, etc.) and ensure compliance with GLP (Good Laboratory Practices) throughout the study process. Contribute to...

HPLC, Prep HPLC, LCMS, UPLC, and Flash Chromatography. HPLC method development and validation, SOP/IOP preparation, calibration, and documentation. Knowledge of raw material, intermediate, and finished product testing.

Role & responsibilities Serve as the primary subject matter expert for all bioanalytical methods, including method development, validation, and sample analysis. Design and execute complex experiments for the quantification of drug candidates, metabolites, and biomarkers in biological matrices using a variety of platforms (e.g., Ligand Binding Assays, cell-based functional assays). Lead the evaluation, implementation, and troubleshooting of new analytical platforms and technologies to advance the laboratory's capabilities. Develop and influence bioanalytical strategies for multiple projects across the drug development pipeline. Manage project timelines and resources, serving as the bioanalyti...

Date: 17 Oct 2025 Location: Kolthur Shamirpet, Medchal, TG, IN, 500078 Division: Discovery Services Job Overview The UPLC-MS Analyst is responsible for conducting ultra-performance liquid chromatography and mass spectrometry analyses on a wide variety of samples, including pharmaceutical, environmental, and biological samples. The role involves sample preparation, method development, and analysis using UPLC-MS techniques to identify, quantify, and characterize compounds. The analyst works closely with research and development teams to support studies, ensuring accurate and timely results. Key Responsibilities Operate and maintain UPLC-MS/LCMS systems for the separation, identification, and q...

We are looking for a highly skilled and dedicated professional to join our team as a Forensic Medicine specialist with 0-12 years of experience. The ideal candidate will have an MD in Forensic Medicine. Roles and Responsibility Conduct thorough examinations and analyses of patients to determine the cause of death or nature of injury. Develop and implement effective treatment plans for patients with various medical conditions. Collaborate with other healthcare professionals to provide comprehensive care. Stay updated with the latest developments and advancements in Forensic Medicine. Participate in ongoing education and training to enhance skills and knowledge. Maintain accurate and detailed ...

We are looking for a highly skilled and experienced Forensic Medicine professional with 1 year of experience to join our team in the Healthcare industry. Roles and Responsibility Conduct thorough examinations and analyses of patients to determine the cause of death or nature of disease. Develop and implement effective treatment plans for various medical conditions. Collaborate with other healthcare professionals to provide comprehensive care. Stay updated with the latest developments and advancements in Forensic Medicine. Participate in ongoing education and training to enhance skills and knowledge. Maintain accurate and detailed records of patient information and treatment plans. Job Requir...

We are looking for a highly skilled and dedicated professional to join our team as a Forensic Medicine specialist with 0-8 years of experience. The ideal candidate will have an MD in Forensic Medicine. Roles and Responsibility Conduct thorough examinations and analyses of patients to determine the cause of death or nature of injury. Develop and implement effective treatment plans for patients with various medical conditions. Collaborate with other healthcare professionals to provide comprehensive care. Stay updated with the latest developments and advancements in Forensic Medicine. Participate in ongoing education and training to enhance skills and knowledge. Maintain accurate and detailed r...

We are looking for a highly skilled and experienced professional with 1 year of experience to join our team as a Forensic Medicine expert in Hyderabad, Telangana. The ideal candidate should have an MD in Forensic Medicine. Roles and Responsibility Conduct thorough examinations and analyses of patients to determine the cause of death or nature of injury. Develop and implement effective treatment plans for patients with various medical conditions. Collaborate with other healthcare professionals to provide comprehensive care. Stay updated with the latest developments and advancements in Forensic Medicine. Participate in ongoing education and training to enhance skills and knowledge. Maintain ac...

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department Masters degree level in Chemistry life science,M pharmacy & B pharmacy qualification. 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Bio-analytical: Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the...