111 Hplc Analysis Jobs - Page 2

Ensure GLP,GDP, STPs, SOPs & SOIs. Calibrate & maintain HPLC, Rheometer, Viscometer, balances. Perform analytical methods and Q3/PEQ characterization studies. Protocols,reports,reagents,routine analysis, PSD, rheology, viscosity, and related studies.

Position: Assistant manager Department: QC Location: Ankleshwar, Gujarat Joining : Within 1 Month Roles & Responsibilities: Ensure adherence to GLP, cGMP, safety, and data integrity practices in the laboratory. Perform routine and stability analysis of Raw Materials, Packing Materials, Intermediates, APIs, In-process samples, Finished Products, Returned Goods, Hold Time studies, Working Standards as per specifications, SOPs, and test procedures. Execute HPLC-related analysis with proper online documentation in LIMS. Maintain compliance with CFR 21 Part-11 and good chromatography practices during analysis, integration, and review. Record analytical results in worksheets/protocols, ensuring ac...

Role Overview: You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of the team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. Key Responsibilities: - Conduct HPLC analysis of Solid Orals and Nasal pro...

Designation : Junior Analyst / Analyst / Senior Analyst Department : Residue / N&W Location : Hyderabad Qualification : M.Sc. (Organic Chemistry/Chemistry/Analytical chemistry) Experience : 1 - 5 Years Industry : CRO & Testing Laboratory Roles and Responsibilities: Analysis of Pesticide residues of Food and Agriculture products as per SOPs, IS, AOAC, FSSAI. Method development, validation and report preparation. Operation and Calibration of equipment i.e., LC-MS/MS, GC-MS/MS, Analysis of Pesticide residues in Water samples. Analysis of Antibiotics in Aqua & Marine products, Feed, Milk & Milk products. Analysis of Pesticide Residues in Fruits and vegetables, Milk & Milk products, Feed & Feed P...

Description We are seeking a skilled QA & QC Chemist to join our team in India. The ideal candidate will be responsible for ensuring the quality and safety of our chemical products through rigorous testing and analysis. This role is critical in maintaining our high standards and compliance with industry regulations. Responsibilities Develop and implement quality control procedures for testing and analyzing raw materials, intermediates, and finished products. Conduct routine laboratory tests and analyses to ensure compliance with quality standards. Document and report on the findings of tests and analyses, maintaining accurate records of results. Collaborate with production and R&D teams to a...

Analyze various pharmaceutical materials including: In-process samples Intermediates Raw materials Packing materials Finished products Stability study samples Hold time study samples Process validation samples Cleaning samples Vendor development samples Any other analysis allocated by the team leader. Release analytical results with proper documentation. Take responsibility for ensuring the quality and purity of pharmaceutical products using High-Performance Liquid Chromatography (HPLC) techniques. Prepare samples for HPLC analysis according to established Standard Operating Procedures (SOPs) and specifications. Analyze HPLC data, interpret results, and generate reports documenting test resu...

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 IS...

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 a...

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 thi...

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 res...

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 ac...

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 cal...

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. F...

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 ...

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 Ra...

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 sa...

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