80 Hplc Analysis Jobs

JOB SPECIFICATION OF JOB TITLE Analyst LOCATION FTL Pune DEPARTMENT Instrumentation (HPLC Section ) REPORTING TO Sameer Lokhande / Dr. Bharat Ugare EXPERIENCE 3-5 Yrs + QUALIFICATION MSc - in Analytical Chemistry/ Inorganic and organic Chemistry / Biochemistry JOB RESPONSIBILITY Handling operating of HPLC. Should have experience of new method development on HPLC. Responsible for Sugar Profile, Amino Acid , Aflatoxins, Benzoic Acid, Sorbic Acid, Vitamins Analysis, Colour Analysis etc... Thorough Knowledge of SANTE 11312 and EU 808 guidelines is desired. Should be familiar with regulatory requirements of FSSAI, EIC, APEDA and Tea Board. Should have experience in implementation of QMS as per ISO-17025:2017 & Responsible for Analysis Sugar Profile, Amino Acid , Aflatoxins, Benzoic Acid, Sorbic Acid, Vitamins Analysis, Colour Analysis in all Food products, Fish, Meat and Animal origin product category samples. Must face min. 1-2 times Integrated Assessment of NABL. Thorough Knowledge of ISO:17025:2017 ATTRIBUTES Good written and spoken English (knowledge of local language is advantageous). Excellent communication and presentation skills Good Listening ability ¢ Good Analytical skills ¢ Good Team Player

Responsibilities: * Conduct HPLC & GC analyses with accuracy * Ensure method validation meets standards * Develop testing processes using SOPs * Collaborate on quality control initiatives * Manage analytical instruments effectively

We have a great opportunity in a reputed Pharmaceutical Manufacturing Company in Vapi, Gujarat. Minimum 5 -8 years of experience B.Sc/ M.Sc in Chemistry, B Pharma/ M Pharma- with FDA Approval Attractive Salary Required Candidate profile Interested candidates may share their updated CV at hire@hireindians.com or Call/WhatsApp at 8882212450.

Job Title: Quality Control Chemist Company: Ambrosia Remedies Pvt. Ltd. Location: Waghodia GIDC, Vadodara Experience Required: 13 Years CTC: 3.0 4.0 LPA About the Company Ambrosia Remedies Pvt. Ltd. is a fast-growing pharmaceutical company dedicated to delivering safe, effective, and high-quality healthcare solutions. We are committed to maintaining global quality standards while ensuring compliance with regulatory norms. Job Responsibilities Conduct quality control testing of raw materials, Packing materials, intermediates, and finished products as per defined specifications. Perform analysis using analytical instruments such as HPLC, UV, and other relevant techniques/Instruments. Monitor and test purified water, effluent water, and other utilities as per regulatory requirements. Prepare and maintain accurate documentation, analytical reports, and test records in line with WHO and GMP guidelines. Ensure adherence to Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLP). Participate in audits, validations, and continuous improvement activities in the QC department. Collaborate with production and QA teams to ensure consistent product quality. Key Skills & Competencies Proficiency in analytical techniques (HPLC, UV, Titrations, etc.). Strong knowledge of regulatory guidelines (WHO, GMP, GLP). Good documentation and reporting skills. Problem-solving mindset with attention to detail. Ability to work under timelines and in a team environment. Approval as Technical Person from FDA is preferred. Educational Qualification B.Sc. / M.Sc. in Chemistry / Pharmaceutical Chemistry / Industrial Chemistry Why Join Us? Opportunity to work with advanced analytical instruments and techniques. Exposure to international quality standards and compliance requirements. Career growth in a professional and supportive work environment.

Role: Officer - Quality Control / Quality Assurance Job Location: Nashik At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products and services. Every day, we rise to the challenge to make a difference and here's how this role, will make an impact: Role Purpose We have Openings in Both QC (Lab / Microbiology / CSV) and QA(IPQA / Documentation / QMS / AQA) . Seeking for candidates (Male/Female) with sound qualification background to ensure the testing of drug product in Quality control lab and to ensure every product is of the highest quality. They shall be concerned with sampling, specifications, testing, documentation, release procedures which ensure that the necessary and relevant tests are carried out under the norms of cGMP. Role & responsibilities Candidate must have relevant experience in Quality control OSD and QMS and able to operate & maintain laboratory equipment/instruments (HPLC, GC, Malvern Particle sizer, dissolution apparatus etc.) as per procedure. To maintain documents as per GLP requirements. To ensure the calibration status of laboratory equipment & instruments. To report and involve in incidence/Deviation/OOS/OOT investigations. Candidate must have sound exposure in the Quality Control Laboratory to supervise and maintain documents and retention of records as per GMP requirements. To ensure the review of QC documents like analytical reports SOPS, Qualification, Logbooks, Raw data sheet, analytical records, calibration and ensuring compliance to observations with proper root cause and justifications. Candidates participate in initiation, review, and closure of OOS/OOT and monitor the CAPA with implementation in Track wise. To ensure the compliance of the Corrective and Preventive Actions (CAPA) necessitated through various activities such as Regulatory Audits, Market Complaints, and Product Recall & Annual Product Review in the QC if applicable. To support Quality Assurance / Compliance /Regulatory Systems, Processes and ensure Monitoring, Execution, Initiation of the Quality Management Systems in Quality Control laboratory. Qualification & Experience Candidate must be B. Pharm/ M. Pharma/ M. Sc In Chemistry Experience- Candidate must have 1 to 4 years experience in a reputed pharma industry. Candidates must be willing to work in shifts Candidate who have faced regulatory Audits like FDA & MHRA Audit will be preferred.

HPLC -GC Analysis and Reporting, Perform and Monitoring Total Lab Activity, wet lab Analysis , Create and maintain documents for Routine Operation. work distribution and team work, Monitor calibration and preventive maintenance Required Candidate profile Must Efficient hand on HPLC- GC analysis. Problem solving in HPLC, GC and wet lab analysis, having exp. of wet analysis like Titration, gravimetry, UV, Polarimetry, water analysis

You will be responsible for monitoring individuals involved in raw material sampling and analysis on a daily basis. You will troubleshoot and resolve any issues that arise during the analysis of raw materials by analysts. Additionally, you will oversee the handling of the raw material section, starting from sampling to the release of raw materials. It is essential for you to possess knowledge of ERP and LIMS, as well as expertise in chemical tests and HPLC analysis. You will also be involved in managing Quality Management Systems (QMS) such as incidents and Out of Specification (OOS) results. Guiding individuals for compliance in accordance with regulatory norms will also be part of your responsibilities. The ideal candidate for this position should have 12-15 years of relevant experience. The role is designated as Senior Executive / Assistant Manager, and candidates from Ahmedabad will be given preference. Our company offers a comprehensive Promotion Policy, a supportive work environment, job security, free transportation, quality food, and subsidized lunch/dinner. It is important to note that we do not have any bond policy in place.,

Hi we are hiring Position;- QC Officer & Executives QC Officer & Executives Location- Baddi Experience- 2-6 years (HPLC analyst ) Salary Range- 20-30 K Interested candidate Apply Mail ;-Tisha.singh@unitedgroupmail.com Contact No;- 9041666549

The ideal candidate will be responsible for method development and validation, as well as routine and stability analysis utilising a variety of analytical techniques, including (HPLC), GC), Dissolution testing, and Karl Fischer titration.

Job Summary: We are seeking a motivated and detail-oriented fresher to join our Analytical Chemistry team focused on small molecule analysis. The role involves working with advanced analytical instruments and supporting the development, validation, and quality testing of small molecule compounds in a pharmaceutical or chemical environment. Key Responsibilities: Assist in the analysis of small molecules using techniques such as NMR, HPLC, GC, UV, IR, and dissolution testing Prepare analytical test reports and maintain laboratory documentation in compliance with GLP/GMP guidelines Support method development and routine analysis under supervision Calibrate and maintain analytical instruments according to SOPs Follow safety protocols and ensure proper handling of chemicals and laboratory equipment Perform sample preparation, standardization, and solution preparations Assist in stability studies and impurity profiling of Compounds Participate in internal audits and regulatory inspections as needed Required Skills & Knowledge: Basic knowledge of analytical chemistry techniques such as NMR, HPLC, GC, UV-Vis, FTIR Understanding of small molecule behavior and common analytical challenges Familiarity with analytical documentation Good laboratory practices and attention to detail Willingness to learn and adapt in a fast-paced laboratory environment What We Offer: Hands-on training in modern analytical techniques and instrumentation Opportunity to work on real-time R&D and QC projects Exposure to regulatory and quality systems in a pharma/chemical setting A collaborative and learning-focused environment for career growth.

We are looking for skilled Analysts with expertise in HPLC and GC techniques for immediate joining. The candidate will conduct analytical testing to ensure pharmaceutical product quality, develop and validate analytical methods, and contribute to continuous laboratory improvement initiatives. Key Responsibilities: Perform analytical testing using HPLC, GC, UV-Vis, ICP-MS, and LC-MS techniques to assess product quality and purity. Develop, validate, and optimize analytical methods in compliance with cGMP guidelines. Collaborate with cross-functional teams to troubleshoot and resolve method validation and analytical issues. Maintain detailed and accurate records of test results, instrument calibrations, and maintenance schedules. Participate in continuous improvement projects to enhance laboratory efficiency and accuracy. Required Qualifications: Bachelors degree in Pharmacy (B.Pharma) or equivalent. Postgraduate qualifications such as M.Pharma, MS/M.Sc in Pharmacology, Food Technology, Biotechnology, Biochemistry, Biology, or Microbiology are preferred. 2-7 years of relevant experience in pharmaceutical analytical laboratories. Strong knowledge and hands-on experience with HPLC, GC, UV-Vis, ICP-MS, and LC-MS instruments. Familiarity with cGMP guidelines and pharmaceutical quality standards. Excellent documentation and analytical skills. Preferred Skills: Experience in method development and validation. Good understanding of pharmaceutical regulatory requirements. Ability to work effectively in a team-oriented environment.

Walk In Drive For Quality Control Department In Formulation Division @ Bollaram Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 6 Years Division :- Formulation Interview Date:-06-09-2025 Interview Time:- 9AM TO 4.00PM Work Location :- MSNF-I, Bollaram Venue Location :- MSN Laboratories Pvt Ltd (Formulation Div I) Plot No:-42,Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana-502325. (View on map) Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Walk-In Interview Date: 3rd,4th & 5 September 2025(Wednesday , Thursday & Friday) Timing: 09:30 A.M. to 4:00 P.M. Venue: Umedica Laboratories Pvt. Ltd. Plot No. Plot No. 221 & 221/1,GIDC, IInd Phase Vapi 396195 ,Gujarat 1. Quality Control Position: QC Officer Candidates having educational qualification of BSc/MSc with specialization in Chemistry. Organic chemistry/Analytical chemcistry with experience of 2 to 5 years in Quality control Departments. Working exposure in HPLC, GC, etc. Qualification: M.Sc. Chemistry / BSc. Experience: 2-5 Years No. of Vacant Position: 20 2. Engineering Position : Officer / Sr. Officer / Executive Should Have Sound Knowledge of PLC Scada Instrument have related to Mfg Area (Osd, Injection), Plant Maintenance, Utility area & EHS Activity. Qualification : B.E / B. Tech - Mechanical Experience : 3 - 8 Years No. of Vacancies : 05 Kindly carry below listed documents during interview. 1. Latest Passport size photo 2. Latest updated resume 3. Xerox copy of Qualification Certificates 4. Salary Slip / Appointment letter copy of current company / CTC Proof & Bank Statement (Last 3 Months )

Role & responsibilities : 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Preferred candidate profile

Role & responsibilities Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Analysis of raw material / finished products / stability samples / Dissolution profiling for R&D/ Plant support. Analytical Method Development /Verification Assay, Related substances, Dissolution etc . Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hot Air Oven, Refrigerator temperature monitoring. Develop/ optimize the analytical methods by Chemical/ instrument analysis Verify/ validate the analytical methods by Chemical/ instrument analysis Preparation / Revision of Specification and Method of analysis for Raw materials / Finished Product / Inactive / Excipients etc Appropriate documentation of results and calculations, preparation of SOPs, specifications and test methods. Interpret results, evaluate data, draw relevant conclusions and give timely feedback to concerned Departments. Analytical Technology transfer of analytical methods by Chemical/ instrument analysis Perform the Impurity standard/ working standard/ primary reference standards. Receiving and filling controlled copy of specifications / method of analysis / SOP / STP etc Operation of various software like Oasis LIMS, Q Edge TMS, Chromeleon etc Preferred candidate profile Qualification: B. Pharm / M.Pharm / M. Sc Experience: Minimum 2 years in HPLC Analysis Development and Validation Perks and benefits Mediclaim

The role involves handling various responsibilities related to Wet Analysis, Specification Preparation, CCF Handling, and Instrumentation such as HPLC and GC Analysis. The ideal candidate for this position should have a qualification of M.Sc. in Chemistry, B. Pharmacy, or M. Pharmacy.,

This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To perform HPLC and Dissolution analysis. To review and check all Raw material, packing material, bulk and finish product specification, method of analysis and all worksheet. To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials. To ensure for timely analysis of bulk, finish product, stability sample and validation sample. Qualifications / Requirements: Experience of performing HPLC analysis. Bachelors degree in a scientific discipline (Masters Preferred). 3-7+ years of hands-on experience in the pharmaceutical industry, with specific experience in Quality Control. Job Types: Full-time, Permanent Schedule: Day shift Yearly bonus License/Certification: FDA certification Chemical and Physio Chemical Testing. (Required) Work Location: In person,

Design & develop API/intermediate processes, optimize & validate methods, analyze data (HPLC, GC, NMR, IR, MS), impurity profiling, documentation, lab record management & equipment maintenance. Required Candidate profile 1 - 5 years of experience BSc./ MSc. in Chemistry

Design & develop API/intermediates processes, optimize & validate methods, analyze data (HPLC, GC, NMR, IR, MS), handle impurity profiling, maintain documentation & lab records, and ensure equipment upkeep. Required Candidate profile 6-8 Years of experience BSc./ MSc. in Chemistry

Quality Control Analysts needed with 4+ years of experience in HPLC/GC, troubleshooting, and software integration (mpower 3, LIMS). GMP, GLP, GDP, and DI knowledge required. Shift operations experience necessary. Pharma API experience Mandatory.

Role & responsibilities CSV validation, ensuring compliance with industry standards and regulations. Documentation of URS, validation plans, protocols, reports and risk assessments. Having sound knowledge in Gxp (GMP,GDP,GLP). Preparation and review of Gap assessment protocols. Preparation and review of IQ,OQ,PQ protocols & test scripts and documented the results. Preparation and review of Functional Risk Assessments (FRA). Preparation and review of Requirement traceability matrix (RTM) & Validation summary report Preferred candidate profile Bsc/Msc in chemistry with 3 to 5 years of experience in Computer System Validation in the Quality control department (API Industry ) only male candidates can attend interview .

Post: Officer - QC Experience: 1-5 Years Qualification: M.Sc No. of Vacancy: 3 Nos. JOB RESPONSIBILITY :- Responsible for sampling and Instrumental/chemical analysis of RM, In-Process, Intermediate, Finished product, Cleaning samples, Validation samples, Market samples and Stability samples. Responsible to perform the calibration of instrument/equipment available in Quality Control laboratory. Maintain the laboratory as per GLP and GMP System. Sampling, Analysis, and review of raw material/packing material, Wet analysis i.e., water content, IR, UV, LOD, Assay by potentiometry, Sulphated ash etc, finished goods sampling, working on HPLC & GC instrument. Interested candidates can share CVs at jhelam.s@randstad.in

Responsibilities: * Conduct HPLC & GC analyses with accuracy * Ensure method validation meets standards * Develop testing processes using SOPs * Collaborate on quality control initiatives * Manage analytical instruments effectively

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

Key Skills: Hands-on experience in HPLC handling . Proficiency in Empower3 software . Strong knowledge and practical exposure to instrument analysis . This is a walk-in post. Even then candidates are encouraged to share their resumes in advance at talenthire-unit4@metroapi.com with the subject line Profile for Quality Control . This will help our team connect with you beforehand and guide you about the position. We warmly welcome candidates who are currently working in Visakhapatnam and nearby areas. Note: Candidates with relevant skills in the Quality Control department are requested to apply for this position. .