568 Lcms Jobs

Job description: Conduct in vitro ADME studies such as solubility, stability, plasma protein binding, metabolism, drug-drug interactions, and Caco-2 permeability Instrumental in bioanalytical sample preparation, LC-MS/MS data acquisition and integration. Recording of raw data, data acquisition, compilation, analysis, and interpretation. Ensure data integrity and reporting with good accuracy. Prepare study plans and reports. Maintain the laboratory and equipment as per SOP. Perform assigned work independently with minimum supervision. Skills Required: Masters in Pharmacy/ biotech/ chemistry/ biochemistry or relevant field with experience of 1-4 years Good verbal and written communication skil...

Need a Jr Analyst for a food testing lab.candidates having experience in GCMSMS/LCMSMS are preferred.need to join immediately

5+ years of hands-on experience in designing, developing, and deploying applications on Microsoft Azure Cloud platforms.?Strong expertise in Azure Logic Apps for workflow automation and system integration.?Proficient in developing and maintaining Azure Functions (Python-based serverless solutions) ?Experience with Azure Storage (Blob, Table, Queue) ?Skilled in managing and deploying microservices using Azure Service Fabric.? Hands-on experience with Azure API Management for API lifecycle management, throttling, and security enforcement.?Proficient in REST API design, development, and integration, ensuring seamless connectivity across systems.? Solid understanding of Azure Security best pract...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Around 4-7 years of relevant experience in handling life cycle management (LCM) of approved/marketed drug products (small molecules as well as biologicals ...

Job Title: Manager Instrument Lab Location:[Jodhpur,Rajasthan] Department: Instrument Lab Reports To: General Manager Job Summary: The Manager – Instrument Lab holds a team-leader role overseeing all operations of the Instrument Laboratory and Instrumental Analysis. This role demands strategic oversight, technical expertise, team leadership, and compliance with global regulatory standards. The Manager is responsible for ensuring the lab delivers accurate, timely, and reliable analytical results and supports quality control and development as per regulatory needs. KEY RESPONSIBILITIES: LEADERSHIP & STRATEGY Provide strategic direction for Instrument lab operations and continuous improvement. ...

Roles and Responsibilities Conduct analytical method validation, including preparing methods, running samples, and reporting results. Perform routine maintenance of laboratory equipment such as GC-MS, HPLC, LCMS, and other chromatography systems. Develop and maintain calibration protocols for instrument qualification and preventive maintenance schedules. Collaborate with cross-functional teams to resolve issues related to analytical testing and method development. Ensure compliance with regulatory requirements by maintaining accurate records of test data and reports.

test house/ Lab

The HRMS and Omics/Biologics Market Development Manager is responsible for developing business, drive market development initiatives, promote newer technologies and create growth opportunities. This role combines strategic marketing with technical proficiency, deep and advance knowledge to shape business performance and is required to understand the challenges of High Resolution Mass Spectrometers (HRMS) products applications to diverse segment customers. Responsibilities: Promote newer HRMS technology products, providing guidance, training, and mentorship to ensure alignment with organizational goals and continuous team growth. Analyze HRMS market trends and competitive information to ident...

Job Purpose: We are seeking a candidate to be part of a team focused on innovation in formulation technology including drone applicable, nano technology. The candidate will work with a multidisciplinary team of scientists and be engaged in targeted formulation development and optimization. Responsibilities: Design and implement experiments for the formulation specially for Drone application and characterization of surfactant, polymer, lipid and other delivery chemistry for in drone application. Formulation and characterization of drone ready formulation for platform build and project support Lead and participate in the assessment and development of early-stage formulation development activit...

Good communication skills. Basic analytical chemistry knowledge. Hands on experience with HPLC/ LCMS / GCMS Method development skills Qualification Groups Post Graduation M.Sc Post Graduation MHRM

Role & responsibilities Managing the day-to-day operation of the concerned department in a complying and in safe manner. Preparing and issuing the job descriptions to the concerned team member. To ensure that only current and authorized documents are being used in the department. Verification of log books and raw data. Verifying the accuracy and validity of technical data, ensuring its proper recording and archiving. Review of method development, verification, validation, protocols, reports and raw data. Supervise and participate in developing, validating, and transferring analytical methods for drug product testing. Ensure all testing procedures comply with established protocols, maintainin...

1. Method development and validation of Genotoxic impurities/ nitroso amine impurities/NDSRIs in pharmaceutical products/ substances by LC-MS/MS. 2. Method development and validation of Genotoxic impurities/ nitroso amine impurities in pharmaceutical products/ substances by GC-MS/MS. 3. Development of MS compatible methods for the HPLC RS methods for the identification of unknown peaks by LC-MS 4. Development of MS compatible methods for the identification of degradation impurities and unknown impurities

Role Overview: As a Scientist at USP, you will play a crucial role in conducting analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your expertise will enhance the laboratory's scientific proficiency and work ethic by providing technical support and knowledge. You will be proficient in various laboratory techniques and capable of offering valuable observations and insights into challenging projects. Your responsibilities will include executing analytical tests, preparing summary reports, and contributing to the Verification Program. Key Responsibilities: - Conduct verification projects on Dietary Supplements/Dietary Ingredients by perfo...

Role Overview: As a Scientist at USP, you will be responsible for conducting necessary analytical tests on Verification samples (Dietary supplements/Dietary Ingredients) using suitable methods. Your role will involve enhancing the laboratory's scientific proficiency and work ethic by providing extensive technical support and knowledge. You will be proficient in various common laboratory techniques, offering valuable observations and insights into challenging projects. Your primary responsibility will be to provide technical aid to the Verification Program by executing analytical tests and preparing comprehensive summary reports. Key Responsibilities: - Conduct verification projects on Dietar...

In this role at Amneal, you will be responsible for conducting extractables and leachable studies on packaging components, medical devices, and drug products. Your key responsibilities will include: - Performing sample preparation, extraction, and analysis using techniques such as HPLC, GC-MS, LC-MS, ICP MS, ICP OES, and other relevant instrumentation. - Developing and validating analytical methods for E&L testing in compliance with regulatory guidelines (e.g., USP). - Interpreting and reporting analytical data, including the identification and quantification of unknown compounds. - Preparing technical reports, protocols, and documentation for regulatory submissions. - Maintaining laboratory...

As a Scientist at Novartis, you will be responsible for planning and performing scientific experiments for the preparation and timely delivery of drug substances, drug products, processes, and procedures. You will collaborate within a multifunctional project team coordinated by a Project Leader and contribute to the maintenance of lab instruments and infrastructure. Your responsibilities will include: - Meeting quality, quantity, and timelines in all assigned projects - Performing and documenting scientific experiments - Planning and organizing scientific experiments under minimal guidance - Providing documentation of raw data and evaluating results - Proposing design for next experiments an...

Responsible for all analytical activities in a small molecule Drug Discovery and Development environment. Driving analytical method development, characterization, and development support from early discovery through latest age and manufacturing.

As a Senior 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 developing, validating, and applying modern analytical technologies to support the development and commercialization of agricultural products. You will play a key role in ensuring that FMC's quality standards and good laboratory practices are upheld at the Toller site. Additionally, you will collaborate closely with synthetic chemists and engineers to provide analytical support as required. **Key Responsibilities:** - Know, understand, and practice all aspects of laboratory safety and industrial hygiene protoc...

Corelate the material level knowledge to the electrochemistry of the device Define specification for materials for electrochemical systems considering the efficiency and reliability impacts Study new techniques and developments in electrochemical engineering and incorporate them Analysis and develop new materials, processes and testing methodologies for Electrolyser components. Execute material level tests that will expand the knowledge on components Lead problem solving activities on component and device level Collaboration with cross functional engineers Support relevant activities in lab and pilot scale operations. Support the characterization of materials using advanced techniques, anayl...

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...

JOIN OUR GROWING TEAM! WE ARE RECRUITING FOR OUR UNIT II (R&D), MORAIYA WALK-IN INTERVIEW ADL Interview Venue Unison Pharmaceuticals Pvt. Ltd. SAFAL PEGASUS , Block A, Office Number: 905, 6, 7, 8, 100 Feet Anand Nagar Road, Chinar Bungalows, Prahlad Nagar, Ahmedabad, Gujarat 380015 Website: www.unisonpharmaceuticals.com If you want, I can also convert this into a Word/PDF , WhatsApp-friendly message , or poster caption . UNISON PHARMACEUTICALS PVT. LTD. 7th December 2025 (Sunday) Time: 9:30 A.M. – 3:30 P.M. NUMBER OF POSITIONS – 15 (REGULATED MARKET) Job Details 1. ADL – Method Development (OSD) Designation: Officer / Sr. Officer / Executive / Sr. Executive Experience: 2–8 Years Qualificatio...

Walk-In Drive for Multiple Positions at Daicel Chiral Technologies (India)Limited Department: Synthesis R&D Job role: Trainee Chemist/Sr. Chemist / JRA /RA Qualification: M. Sc (Organic Chemistry/Medicinal Chemistry) Experience: 0-5 Years Job Discription: Proficient in performing a wide range of reactions in synthetic organic chemistry. Skilled in handling reaction scales from milligrams to kilograms. Experienced in purification techniques such as column chromatography, recrystallization, and preparative TLC. Well-versed in chromatographic methods including TLC and column chromatography. Competent in computer applications such as ChemDraw, MS Word, Excel, and electronic lab notebook document...

Walk-In Drive for Multiple Positions at Daicel Chiral Technologies (India)Limited Department: Pharma Standard - AD Job role: Trainee Chemist/Sr. Chemist / JRA Experience: 0-4 Years Required Qualification & Experience & Skills: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 4 Years of experience in the field of pharmaceutical industry/CRO setup. Develop preparative suitable methods by HPLC & SFC . Execution of Chiral separation, Purification and impurity isolation activities by preparative HPLC, SFC, LCMS. Expertise in Purification of peptides, Oligonucleotides impurity isolation. **************************************************************************** Department: Pharma Sta...

Role & responsibilities Job Responsibilities: 1. Handling of stability section independently. 2. Handling of additional stability studies, such as, Photo stability, In-use studies, freeze thaw studies. Split studies etc. 3. Preparation of stability protocols, reports and stability compilation. 4. Responsible for timely initiation, closure of QMS documents related Quality Control and implementation respective corrective and preventive action. (i.e. Change controls, Laboratory Incidents, OOS, OOT & CAPA) 5. Responsible to follow ALCOA + principle while doing the data recording. 6. Review of In-process, finished, stability, process validation, in-process, Raw material, Excipients, packing mater...

Role Overview: You will be working as a Sr. Scientist I in the India Biologics department at USP, in a hands-on, non-supervisory role. Your main responsibility will be to collaborate in the development of reference standards for biotechnology pharmaceutical products. You will also be involved in supporting the suitability program by preparing and reviewing testing protocols, providing technical assistance to testing labs, and reviewing analytical data to confirm the continued suitability of USP Reference Standards. Key Responsibilities: - Maintain smooth collaboration with key stakeholders to develop reference standards for biotechnology pharmaceutical products - Draft protocols, reports, an...