575 Lcms Jobs - Page 16

1) Preparationof Analytical method validation Protocols and reports for the relatedsubstances and Assay by HPLC and residual solvents by GC 2) Preparation of Analytical methodvalidation Protocols and reports for the Identification analysis by HPLC,GC andparticle size analyzer and performing the analytical method validations for theIdentification, content and purity analysis by HPLC,GC and Particle sizeanalyzer. 3) Performing the Analytical methodvalidations by HPLC and GC. 4) R esponsible to follow and ensure strict compliance to GLP practices in the laboratory to meet the organizational goal which in line with procedural references. 5) Maintenance of log books and Calibration records as per...

Development and validation of analytical methods for injectable dosage forms Stability study execution and data interpretation Support for formulation development and regulatory submissions (US/EU) Instrument handling: HPLC, GC, UV, KF, etc. Preparation of method validation reports, protocols, and SOPs

1) Experience in preparing and reviewing of Method Development Report. 2) Knowledge of ICH Guidelines. 3) Strategic planning and performing Validation studies, Solubility Studies, Impurity and Standard Qualification. 4) Exposure of working on HPLC, LCMS, GC, UV and other equipment. 5) Ability to perform an analysis of related substances, assays and purity by using HPLC, IC. 6) Ability to perform analysis of residual solvents by using gas Chromatography. 7) Preparation and Review of development and validation/ method transfers/ protocols and reports based on R&D qualifications or monographs. 8) Ability to work in a team and contribute towards collective goals.

As the Lead Specialist GOE CAL at dsm-firmenich in Mumbai, you play a crucial role in bridging the gap between taste, texture, and health through innovative ingredients and solutions. Diversity, Equity & Inclusion is at the core of our values, ensuring equal access to opportunities, a sense of belonging, and authenticity celebrated across the organization. Your responsibilities include planning and conducting analytical techniques such as GC-MS, LC-MS for flavors, perfumes, and natural products, contributing to method development and the team's technical growth. You will manage analytical instruments, lab operations, ensure SOP compliance, accurate documentation, and collaborate closely with...

MEDI ANALYTIKA IS RECOGNIZED AS THE LARGEST INSTRUMENTATION COMPANY IN INDIA HAVING TIE UPS WITH 50+ WORLD LEADING INSTRUMENTATION COMPANIES FROM USA - CANADA - UK - EUROPE - JAPAN - REPUBLIC OF KOREA - ISRAEL. Our existing clients include all major universities, research institutions, hospitals, pharmaceutical / CROs, food processing companies, chemical industries and other industries. Role & responsibilities : As a service engineer, you will have to visit our clients spread all over India to install and also provide after sales service support.

Job Title - Organizational Analytics- LMS- Specialist - T&O- (S&C GN) Management Level:09 - Specialist Location:Gurgaon, Mumbai, Bangalore, Kolkata, Pune, Hyderabad, Chennai Must have skills- LMS integration Good to have skills:Cornerstone OnDemand, Saba, SuccessFactors Learning, SumTotal, Docebo Experience:Minimum 5-8 year(s) of experience is required Educational Qualification:Any Bachelors degree Full time Job Summary : Collaborate with leadership to determine the programming objectives. Develop or write codes that support the overall business objectives and strengthen the quality and functionality of business-critical applications to provide optimal functionality. Roles & Responsibilities...

The role of Executive - QC (Stability) at Piramal Pharma Solutions involves conducting stability studies, analyzing samples, preparing reports, and ensuring compliance with regulatory guidelines to maintain product quality throughout its shelf life. You will be working closely with Operations, R & D, QA, and Regulatory affairs teams under the supervision of the QC Supervisor. With a minimum of 3 years of experience in the stability section, you should be a quick learner with excellent communication skills. Punctuality, dedication, and reliability are essential qualities for this role, as well as the ability to work both independently and as part of a team. Proficiency in written and spoken E...

You will be joining our ARD team in Udaipur as an ARD Chemist / Scientist. Your main responsibilities will include method development and validation, impurity profiling, and instrumental analysis to assist our Synthesis R&D and quality operations. Your key responsibilities will include developing HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, validating HPLC methods suitable for AMV, performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, ensuring all analytical instruments are well-maintained, performing regular calibration and documentation of analytical instrume...

Study Analyst Roles and Responsibilities:- General extraction procedures and instrument analysis of drugs in biological fluids. STUDY RELATED ACTIVITIES:- A. Perform the extraction of samples using wet chemistry. B. Centrifuges, evaporators, freeze specimens as required. C. Performs aliquots of samples for wet chemistry. D. Performs wet chemistry according to study protocol guidelines and/or SOPs. E. Completes QC sheets and makes log book entries as required by protocol and/or SOP. F. Operate HPLC, LC/MS/MS and ICP-OES; troubleshoots problems and performs minor repairs. GENERAL LAB DUTIES:- A. Prepares required reagents and solvents. B. Under direction of the project manager, may perform som...

As an ARD Chemist / Scientist at our Udaipur location, you will be a key member of our ARD team, responsible for method development and validation, impurity profiling, and instrumental analysis to support our Synthesis R&D and quality operations. Your primary responsibilities will include developing and validating HPLC, GC, and LC-MS analytical methods for monitoring in-process reaction samples, as well as developing HPLC methods suitable for Analytical Method Validation (AMV) and transfer to QC. You will also be tasked with performing impurity profiling of APIs and intermediates, identifying and characterizing impurities using advanced techniques like mass spectrometry, and ensuring that al...

The Chemist role involves performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. As a Chemist, you will contribute by conducting laboratory testing, preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation, reviewing product certificates of analysis, maintaining Certificates of Analysis (C of A) files, and providing input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents. You will also participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement CAPA with gene...

As a member of the New Chemical Entity(NCE) Research team located in Navi Mumbai, India, your primary responsibility will be the analysis of compounds for various projects from the medicinal chemistry team and lead NCEs. Your role will involve ensuring quality output within the set targets established by the Group leader, with approximately 60% of your time dedicated to this task. Another key aspect of your position will be the development of analytical methods for new NCEs using a range of instrumental techniques such as HPLC, LCMS, NMR, IR, SFC, and other wet analysis methods. This will require a high level of proficiency and attention to detail to deliver quality results within the specif...

SDG is a global cybersecurity, identity governance, risk consulting and advisory company that advises and partners with clients to address their complex security, compliance and technology needs and delivers on strategy, transformation, and long-term management of their cybersecurity and IAM programs. We help some of the largest brands in the world realize their business vision through a mix of strategic advice, expert systems integration, relevant technology recommendations and smart managed services. Our value proposition to our customers is that we bring thought leadership to the table in each of our domains, a passion for customer success, and an eye to risk management in everything we d...

As a Fortune 50 company with more than 400,000 team members worldwide, Target is an iconic brand and one of America's leading retailers. Joining Target means promoting a culture of mutual care and respect and striving to make the most meaningful and positive impact. Becoming a Target team member means joining a community that values different voices and lifts each other up . Here, we believe your unique perspective is important, and you'll build relationships by being authentic and respectful. Overview about TII At Target, we have a timeless purpose and a proven strategy. And that hasnt happened by accident. Some of the best minds from different backgrounds come together at Target to redefin...

Preferred candidate profile M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry / Analytical Chemistry) with 3 - 6 years experience in Bioanalytical DMPK & Invivo PK. Role & responsibilities Planning and execution of invivo preclinical pharmacokinetic studies, invivo tissue distribution & mass balance studies in rodents. Expert in method development of NCEs using LC-MS/MS system Well verse with extraction techniques of molecules from various matrices like plasma/urine/tissues Experienced in surgical skills for rodents PK, excretion studies Conduct Bioanalysis of samples from in-vivo pharmacokinetic, tissue distribution studies, PK-PD & TK studie...

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Qualifications required: Bachelors / Masters in Pharmacy, Msc Chemistry/Organic Chemistry 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 concentrati...

Location - Manufacturing Unit, Bommasandra Qualification - MSc - Chemistry Experience - 2- 5 yrs Role : Analyst LCMS/HRMS Key Job responsibilities: Analyst should able to carryout testing in method transfer and method verification activities. Subject matter expert on analysis of HPLC, LCMS, GCMS for both assay and impurities routine samples of in process, cleaning validation, SFG & Stability. Subject matter expert in analysis of nitrosamine impurities. Subject matter expert calibration of instrument and its management.

Urgent opening for QC Officer-Sr. Officer in Dahej, Bharuch. Note: Walk In Interview at Ahmedabad Date & Time: 20th July, 2025 at 09:00 AM Onwards Job Location: Dahej, Bharuch Experience: 2 to 7 years in API Qualification: M.Sc./B.Pharm/M. Pharm Required Candidate profile Roles and Responsibilities: -Experience in Section LCMS / PSD / HPLC / GC /Method Validation -Candidate preferred from Pharma API (Active Pharmaceutical Ingredient).

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...

Job Title: Peptide Analytical Team Lead; No. of positions: 1 Preferably a M.Sc graduate. Expertise well in the method development for Peptide purification by DAC (Dynamic Axial Compression) column and their analysis part using analytical UPLC instruments. Presently he must work or had experience in SEMAGLUTIDE AND TIRZEPATIDE API's. Should work in analytical lab, overseas the lab members and their day-to-day activities. Should be Conversant with the all the documentation part of analytical department. Performs sample preparation and analysis using analytical HPLC/LCMS for purity and mass for identity. Good knowledge and decision making in proper choice of column for a suitable peptide target...

Interested candidates can share resume to sanjay.behera@thyrocare.com or whatsapp to 8928285213 Key Responsibilities: Operate, calibrate, and maintain ICP-MS and LC-MS instruments according to established SOPs. Prepare samples for analysis, including digestion, dilution, filtration, and extraction techniques. Perform quantitative and qualitative analysis of environmental, biological, food, or pharmaceutical samples. Conduct method development and optimization under guidance of senior staff. Document all laboratory activities, observations, and results accurately in lab notebooks or LIMS. Ensure compliance with all safety, QA/QC, and regulatory standards (e.g., ISO 17025, GLP/GMP). Assist in ...

Job Description Summary This analyst role is responsible to perform analysis of stability samples, Raw materials, analytical method validation/verification and method transfer studies Job Description To perform Nitrosamine & extractable and leachable analysis of analytical method development / validation / verification and method transfer. Handling of LCMS, ICPMS instruments. Knowledge on nitrosamine method development / validation / verification. Experience: 7 to 9 years with M.Sc./ M. Pharm

Hi Jobseeker, Greetings from Laurus Labs! Please find the below positions of current openings at Laurus Labs - Visakhapatnam (Atchutapuram OSD Formulation Unit) Department : Quality Control-OSD Formulations Designation : Associate/Executive Section : Wet Chemistry & LC-MS/GC-MS Interested candidates can send their resume to seetaram.y@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period :

Role & responsibilities Should perform sample processing smoothly as well as project execution with in assign time. Should handle instrument as well as QA observation. Should coordinate with Group members/ Group leader/ Lab manager Should be able to inspect raw data as per defined procedure. Should report inspection result properly. Should verify calibration record. Should maintain GLP in Lab. Preferred candidate profile 5-6 Years of Experience in Clinical Research Organizations only (Bio-Analytical Department) Qualification: MSC Immediate to 20 days joiners are preferred. You can also share your resumes on: pradnya.raut@accutestglobal.com for quicker callback

Preferred Candidate Profile: M. Pharm (Pharmacology / Pharmaceutical Analysis) / M.Sc. (Biochemistry / Pharmaceutical Chemistry / Analytical Chemistry) with 5-8 years or Ph.D. with 2-5 years experience. Role & responsibilities Experience in designing, performing, and interpreting metabolite identification studies- Invitro and Invivo. Proficient in using LC-MS/MS, HRMS, and other analytical techniques for identification of metabolites and its soft spots. Ability to analyze complex data sets and structural interpretation for Phase-1, 2, and 3 metabolites. Strong understanding of drug metabolism principles and pathway. Experience with regulatory documentation and submissions Experience in DMPK ...