111 Hplc Analysis Jobs

Role & responsibilities Handling Water's HPLC Preferred candidate profile HPLC

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC / Microbiology o Qualification & Experience: (02 - 06Years) •B.Sc, B.Pharma & M.Sc with relevant experience o Designations: •Jr. Officer, Officer & Jr.Executive ARD: Stability/ FP /AMV/ HPLC o Qualification & Experience: (02 - 05Years) •B.Sc, B.Pharma , M.Sc & M.Pharma with relevant experience o Designations: •Jr. Research Associate & Research Associate-I INTERVIEW VENUE: o Hotel Le Mariet 9th Km Milestone , Baddi Nalagarh Highway, Krishnapura, Solan, H.P - 174101 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID...

Responsibilities: * Collaborate with cross-functional teams on new product development. * Develop organic chemicals through research and development. *Optimise Process Education- MSc Organic/Industrial Chemistry Exp- 0 to 3 years

QC Chemist for Testing and Quality Control of all types of Pesticide Formulations. Will be testing raw materials, finished products and also assist in formulation developments/process improvements etc. Maintain documents as per NABL Required Candidate profile Strong knowledge of chemistry with hands on experience in HPLC, GC and other dry and wet testing is a must. Candidates from Pesticide Industry would be given preference. Must have NABL experience

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Key Responsibilities: 1. Routine Analysis & Testing: Perform analysis of raw materials, in-process, finished products, and stability samples as per approved specifications and test procedures. Conduct analysis using instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, Dissolution Tester, pH Meter, and KF Titrator . Ensure analytical results are recorded accurately and reviewed as per GLP and cGMP standards. 2. Documentation & Record Keeping: Prepare and review analytical reports, COAs, and test records. Maintain logbooks, stability registers, and instrument usage records. Ensure compliance with Good Documentation Practices (GDP) and data integrity requirements. 3. Instrument Calibra...

HPLC, Prep HPLC, LCMS, UPLC, and Flash Chromatography. HPLC method development and validation, SOP/IOP preparation, calibration, and documentation. Knowledge of raw material, intermediate, and finished product testing.

HPLC analysis to perform for food parameters (e.g., preservatives, additives, vitamins, sweeteners, etc.), operate, calibrate, and maintain HPLC instruments (UV, PDA, RI, or Fluorescence detectors). Ensure ISO/IEC 17025 compliance in testing. Required Candidate profile Minimum 2 years of specific HPLC experience in a NABL-accredited food testing laboratory. a good HPLC candidate from the pharma industry can also apply. Must have faced at least one NABL audit. Perks and benefits Best in the Industry.

Experience - 3 Years + In Formulation QC * QC - Finish Product - GC/HPLC/ Dissolution/AAS/UV * QC- In process- HPLC/UV/Dissolution/GC * QC - Validation- HPLC/UV/GC/Dissolution * RM - HPLC * Stability HPLC GC UV Dissolution * RM Reviewer

JOB DESCRIPTION OF CHEMIST/Sr.CHEMIST An edible oil industry chemist's job description involves performing chemical analyses on raw materials and finished products, troubleshooting quality issues, and ensuring compliance with food safety standards. Key duties include using instruments like GC and HPLC, monitoring quality parameters such as free fatty acids and peroxide value, performing water and effluent testing, and maintaining quality control throughout the production process. Key responsibilities Chemical analysis: Perform a range of analyses on edible oils, refinery by-products, and other materials like water and coal. Quality control: Monitor the quality of raw materials, in-process pr...

Key Responsibilities Method Development and Validation : Conduct analytical method development, verification, validation, and transfers. This includes methods for related substances, assay, residual solvents, and cleaning procedures. Analytical Support : Provide analytical support to process development teams. This involves analyzing samples using instruments such as HPLC (High-Performance Liquid Chromatography) , GC (Gas Chromatography) , IR (Infrared Spectroscopy) , KF Titrator (Karl Fischer Titrator) , SOR (Specific Optical Rotation) , ROI (Residue on Ignition) , and LOD (Loss on Drying) . Documentation and Compliance : Ensure the timely completion of all analysis, documentation, data rev...

Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices. Responsible to perform the Analytical method validation, method verification and method transfer activities.

You will be responsible for conducting WET, GC, and HPLC analysis as an Expert in the field. Your role will involve ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and ALCOA+ guidelines. Key Responsibilities: - Conduct WET, GC, and HPLC analysis - Ensure compliance with GMP, GLP, GDP, and ALCOA+ guidelines Qualification Required: - M.Sc. in Chemistry - 3 to 5 years of experience - Good knowledge of GMP, GLP, GDP, ALCOA+ - Expertise in WET, GC, HPLC Analysis,

Responsibilities: Conduct HPLC, GC, UV, water analyses per BMRR. Implement change controls, manage deviations. Perform API manufacturing, intermediate handling, SRP processing.

Responsibilities: * Conduct HPLC & GC analyses with expertise * Oversee wet analysis processes * Collaborate on instrument calibration schedules Note: We are only looking for Telangana & Andhra Pradesh candidates. Health insurance Food allowance Provident fund

Key Skills: Basic understanding of laboratory practices, analytical techniques, GMP/GLP concepts, and willingness to learn quality systems. Attention to detail, good communication, ability to follow SOPs. Willingness to learn, ability to work in a team, and flexibility to work in shifts . 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.

Roles and Responsibilities Conduct quality control analysis of injectable products using techniques such as HPLC, GC, and dissolution testing. Ensure compliance with regulatory requirements and company standards for product specifications, labeling, and packaging. Develop and maintain documentation for quality control procedures, protocols, and reports. Collaborate with cross-functional teams to resolve issues related to product quality and manufacturing processes. Participate in audits and inspections conducted by regulatory agencies or third-party organizations.

You will be responsible for the execution of analytical method optimization/development, validation/verification of analytical test methods related to Compendia, In-house developed methods, Site transfer methods, Regulatory queries, Method Life Cycle Management (MLCM) studies, Supplier Driven Changes (SDC), and other procedural updations. This includes the preparation of method validation/verification protocols and reports. Your key responsibilities will include: - Executing method optimization/development studies. - Validating/verifying in-house methods, Compendia, SDC, MLCM, and Cleaning Analytical methods while adhering to regulatory procedures. - Preparing Method verification/Method tran...

B.Sc./M.Sc. with 1–4 years in QC (API). Hands-on with HPLC, GC, UV, and wet analysis. Experienced in raw material, in-process, and finished product testing. Strong in GMP, documentation, and analytical techniques. Required Candidate profile B.Sc./M.Sc. with 1–4 years’ QC experience in API. Proficient in HPLC, GC, wet lab testing, and GMP documentation. Detail-oriented, accurate, and skilled in analytical methods. Perks and benefits GMP GLP plant| Growth| Safety| Compliance| Perks

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Kindly read the below details and then apply Immediate Hiring !!!! Location: Cuddalore, Tamil Nadu Interview Mode: Level1 : Virtual (Mircosoft Teams) Level 2 : Face to Face Role & responsibilities QC Analyst (IC/HPLC) Experience: Minimum 5-8 years in core area (IC/HPLC and wet analysis) Educational qualification: Only Postgraduate in Chemistry/equivalent Work background: Only Pharma (API/Formulation/excipients) Key responsibilities: 1. Hands on experience on Ion Chromatography is most preferable. 2. Responsible for independently handling IC/HPLC analysis. 3. Qualification and troubleshooting of HPLC instruments. 4. Shall have handled software including Chromoleon 5. Shall have good knowledge...

1. Amino acid validation. 2. In-Process and finished products analysis. 3. Product development product analysis. 4. Documentation. 5. Responsible for method process Share resume to hrd@stedmanpharma.com, Call 7904827192/9786920463 Perks and benefits Canteen and other welfare benefits.

To perform Analytical test method validation. To operate GC and HPLC To prepare working Standards To Maintain and calibrate R&D instruments and record it To prepare certificate analysis, routine protocols and related documents.