570 Lcms Jobs - Page 7

Job Description Role:- Analytical Chemist Key Responsibilities: Performing analysis using state-of-the-art instruments such as HPLC/LC-MS, GC /GC-MS, ICP-OES / ICP-MS (MS-Mass Spectrometer) Ensuring finished goods/samples analysis as per agreed terms of the customer and timelines. Optimize analytical methods, perform validation experiments as per IP/BP/FDA/USP/ ICH guidelines, Develop innovative analytical methods to overcome analytical challenges and achieve project objectives. Collaborate with R & D, T&D and Production departments to support the optimization of synthetic processes. Preparation of SOPs. Consistently delivering analytical data on time Ensure safety at workplace-safe handling...

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...

Hiring for a leading speciality chemical manufacturing company having multiple manufacturing facilities in India. R&D is based out of Hyderabad. Designation: Dy Manager / Asst. Manager - R&D Analytical Chemist Key Responsibilities: Performing analysis using state-of-the-art instruments such as HPLC/LC-MS, GC /GC-MS, ICP-OES / ICP-MS (MS-Mass Spectrometer) Ensuring finished goods/samples analysis as per agreed terms of the customer and timelines. Optimize analytical methods, perform validation experiments as per IP/BP/FDA/USP/ ICH guidelines, Develop innovative analytical methods to overcome analytical challenges and achieve project objectives. Collaborate with R & D, T&D and Production depar...

- Operation and Calibration of LCMS - Method Development and Validation for Nitrosamines and Genotoxic impurity by LCMS - Extractable and Leachable study by LCMS - Mass Interpretation by LCMS - Unknown Peaks Identification by LCMS Required Candidate profile Experience - 2-6 years of relevant experience in Analytical Method Development- -LCMSLocation : Andheri Mumbai Qualification: M. Pharm or MSc Organic Chemistry/Analytical Chemistry

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...

As a Review Analyst at Piramal Pharma Solutions (PPS) located in Digwal, your role will involve reviewing analytical reports and handling investigation incidents. You will be responsible for the following key responsibilities: - Review in-process analytical data before release - Review intermediates, stability batches, and finished products analytical data - Knowledge on analytical method validations and method transfers - Review system audit trails for all types of instruments in QC - Review calibration data of instruments on a daily basis - Verify SOPs compliance on the shop floor - Conduct audits for laboratory system compliances as required - Investigate incidents, OOS, OOT, and root cau...

Your Role Total Experience of at least 7-8 years of IT experience with 4-8 years of Identity Management and at least 4-5 years of relevant SailPoint IIQ implementation experience. Strong experience in architecting IAM solutions using SailPoint IIQ Experienced in executing the role mining module Strong hands-on development skills in SailPoint and well-versed in creating workflows, rules, custom bean shell, provisioning plan, certifications, LCM, custom connectors, policies, entitlements etc. Experience in integrating with JDBC, Active Directory, Exchange, SAP, ERP etc. Knowledge in web services, XML, SOAP and JMS. Knowledge on the Support life cycle Experience in working on the proposal proce...

As a member of our team, you will play a crucial role in the purification of synthetic compounds using chromatography techniques such as Preparative HPLC, Flash Chromatography, and LC-MS. Your primary responsibility will be to optimize purification methods to ensure the recovery of high-quality compounds. Additionally, you will need to perform routine analytical characterization of purified compounds using techniques like NMR, Mass Spectrometry, and UV Spectroscopy. Your duties will also include maintaining laboratory instruments by ensuring proper calibration and troubleshooting minor technical issues. It will be essential for you to keep detailed records of purification processes, observat...

You are required for a (Lab Analysis) residue lab with the following technical knowledge: - Proficiency in HPLC, GC, LC-MS, GC-MS, ICP-OES, and Instruments Handling. - Completing working tasks and reporting to the department head. - Coordinating with Lab chemists. Qualifications required: - B.Sc or M.Sc in Analytical Chemistry or M.Sc in Biochemistry. You will be working in the Animal Feed / Food industry with 4 to 8 years of experience. The salary offered is attractive and will be based on your experience. An age requirement is set above 25 years. The work location is in Nanjai Uthukuli, Erode. Your point of contact for this job position is K.Rajendran AGM HR (hr@skmpornafoods.com) with con...

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 & responsibilities Roles and Responsibilities : Independently design, develop, validate, and troubleshoot bioanalytical methods for small and large molecules using LC-MS/MS and HPLC under GLP and non-GLP environments. Thorough understanding of bioanalytical method validation and sample analysis in biological matrices. Ability to lead junior team members, manage multiple projects , and interact with clients/regulatory bodies. Ensure efficient utilization of instruments and laboratory resources. Perform advanced operation, calibration, troubleshooting, and maintenance of LC-MS/MS , HPLC, and allied analytical equipment. Knowledge of international bioanalytical regulatory guidelines (USFDA...

As a Bioanalytical Scientist at our company, you will be responsible for: - Developing and validating bioanalytical methods using LCMS and other sophisticated instruments - Carrying out routine calibration of instruments - Demonstrating a thorough knowledge of LCMS, HPLC, HPTLC, GCMS, and other analytical instruments - Ensuring compliance with USFDA guidelines - Utilizing excellent communication skills to effectively coordinate with team members - Displaying good interpersonal and management skills - Holding strong basic knowledge of analytical instruments such as HPLC and LC-MS - Being accountable for group productivity, including the number of samples, analysis quality, quantity, and timel...

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.

,in-processthe ,for leading,for leading,problem-solvingResponsibilities We are looking for a senior professional AGM with a range of 15 to 20 years of experience in Analytical Method Validation for regulated markets. The role involves leading API and excipient method validation across multiple dosage forms and managing a team of 30, including three senior managers. The ideal candidate must be technically strong, experienced in US/EU compliance, and hold an M. Pharm, M.Sc., or Ph.D. Role & responsibilities: Accountable to lead the team for AMV of OSD, Nasal, Injectables, Ophthalmic and Topical dosage formulations. Responsible for RM & PM characterization and documentation. Generate qualificat...

JOB OVERVIEW Executes complex simulations in CFD and Thermal to optimize design and manufacturing. Develops complex Multiphysics simulation methods that meets design requirements in thermal management of Electronic Systems, especially in high-speed transceivers, connectors, and their assemblies. KEY RESPOSBILITIES: 5 to 8 years of industry experience. Expertise in Ansys Workbench. Experience on connector products (Plastic and Sheet Metal parts). Knowledge on material science (Metals, Resins & hyper elastic material) and implement for simulation. Expertise on CAE tools, Optimization techniques, and testing methods. Development & execution of complex Thermal simulation models to optimize manuf...

Responsibilities: Process Improvement: Identify and implement continuous improvements for existing copper chemical manufacturing processes to boost efficiency, cut costs, enhance quality, and ensure safety. Troubleshoot production issues. New Product Development (NPD): Lead the entire NPD pipeline for new copper chemicals, from research and lab trials to pilot, manufacturing scale-up, and commercialization. Develop processes & specifications, and manage documentation. Cross-Functional Collaboration: Work closely with Production for technology transfer and scale-up. Partner with Quality Control (QC) on analytical methods and quality. Engage external experts to accelerate development. Complian...

Responsibilities: Synthetic Chemistry / Lab Work Perform multi-step organic synthesis of target molecules as per project requirements. Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products. Maintain accurate lab records and notebooks (ELN or manual) as per GLP standards. Process Development Assist in the optimization of reaction conditions to improve yield, purity, and scalability. Conduct literature searches and suggest alternative synthetic routes under supervision. Evaluate critical process parameters through small-scale experiments. Analytical Coordination Coordinate with the analytical team for sample submissions, impurity profiling, and m...

Walk-In Interview QC Department (1 to 9 Years Experience) Hyderabad 11th & 12th October On 11th October 2025 (Saturday) Time : 9:00 AM to 3:00 PM Location: 7-2-A2, Hetero Corporate , Industrial Estates, Sanathnagar,Hyderabad-500018 Location: Annora Pharma Private Limited, Sy No.261, Plot No13, Annaram (Village), Ginnaram (mandal), Hyderabad On 12th October 2025 (Sunday ) Time : 9:00 AM to 3:00 PM 3. Location: Hotel Krithunga Restaurant, 01st Floor, Above Reliance Smart, Opposite New Bus Stand, Jadcherla Hiring For: Quality Control (QC) API / Formulations / Injectables Experience Required : 1 to 9 Years Qualification : B.Sc / M.Sc / B.Pharm / M.Pharm Department : Quality Control HPLC, GC, Wet...

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At SCIEX, one of Danaher's 15+ operating companies, our work saves livesand we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As part of SCIEX, you will help to influence life changing research and outcomes, while accelerating your potential. For more than 50 years, we have been empowering our customers to solve the most i...

As a member of the o2h discovery team, your role involves: - Strong knowledge and hands-on experience in LC-MS/SFC/HPLC/Prep. method development for all types of chemistry molecules. - Strong understanding of various column chemistry. - Skilled in troubleshooting, instrument maintenance, and calibration. - Leading, training, coaching, and mentoring a team of motivated young scientists. To qualify for this role, you should: - Have a passion for HPLC/Prep./LCMS/SFC analysis and characterization techniques, along with a willingness for continuous learning and education. - Demonstrate creative thinking to identify new techniques and growth opportunities. - Be highly organized with the capability...

Job Description Provides technical & application services & support to Agilent customers. This includes timely and cost-effective problem resolution with the objective to enhance our customer experience and meet Agilent contractual agreements. Leverage post sales interactions with customers to probe and qualify further revenue opportunities and provides highly qualified leads to sales. Performs a set of required admin tasks to ensure flawless customer service for contract and trade customers. Responsibilities of this position include but are not limited to; Responsible for providing remote post-sales hardware, software technical support and Application support services to external customers ...

As an Executive - QC (Stability), your role involves conducting stability studies, analyzing samples, preparing reports, and ensuring compliance with regulatory guidelines to maintain product quality throughout its shelf life. You will work closely with stakeholders such as Operations, R & D, QA, and Regulatory affairs. Reporting to the QC Supervisor, you should have at least 3 years of experience in the stability section. Key Responsibilities: - Work in the stability section - Handle instruments like HPLC, UV, Culometer, KF-titrator, LCMS, etc. - Conduct stability sample analysis - Charge stability samples - Manage Stability Chamber - Have knowledge of instrument software such as Lab soluti...

Roles and Responsibilities Conduct quality control analysis using HPLC, GC, LCMS, Microbiology techniques for APIs and intermediates. Ensure compliance with cGMP guidelines during stability studies and batch release processes. Collaborate with cross-functional teams to resolve issues related to product quality and regulatory affairs. Develop and maintain documentation for laboratory procedures, protocols, and reports in accordance with company standards. Participate in training programs to enhance knowledge on new technologies and methodologies.

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Wednesday 08-10-2025. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,LCMS,GC,GCMS,PXRD High performance liquid chromatography HPLC,LCMS,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 guideli...