101 Gas Chromatography Jobs - Page 4

Responsibilities: * Conduct quality control tests using HPLC, GC, LCMS methods. * Ensure compliance with industry standards and customer requirements. * Collaborate with production team on process improvements. Thanks RIGHTCHOICE Annual bonus Provident fund Health insurance

Walk In Drive For Quality Control Department In Formulation Division @ Vizag Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 08-06-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- Hotel Cygnett Inn Ramachandra , 31-2-4/5, NH16, opp. All India Radio Station, Kurmannapalem, Visakhapatnam, Andhra Pradesh 530046 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). 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.

NUTRIS CROP SOLUTIONS INDIA PVT.LTD is looking for LAB ANALYST to join our dynamic team and embark on a rewarding career journey. Perform analytical testing of samples to ensure quality and compliance. Record and interpret test results, maintaining accurate documentation. Calibrate and maintain laboratory equipment for optimal performance. Follow safety and regulatory guidelines for laboratory procedures. Collaborate with teams to develop new testing methods and protocols.

Walk In Drive For Quality Control Department In Formulation Division @ Jadcherla Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 01-06-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). 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.

Roles and Responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Ensuring the quality of APIs through testing, analysis, & documentation Sample & inspect raw materials Maintain an accurate & complete record of testing, analysis Investigate deviations from the quality standard Ensure compliance with GMP regulations Required Candidate profile Bachelor's degree in B.Sc/M.Sc Chemistry, B.Pharm/M.Pharm. Previous experience in QC in API pharma manufacturing Strong knowledge of analytical techniques & instrumentation, e.g., HPLC, GC, UV-Vis

Role & responsibilities Dear Candidate, Please provide these mandatory details to Share your bio data to the company Waiting for your Reply Present Company: Present Designation: Present Location Qualification: Total Experience: Present CTC: Expected CTC: Notice Period: No. Of Persons reporting to you: your Reporting to : Native Place: Experience: Qualification: Location: We're Hiring Join Pharma at Panoli! Quality Control (QC) Pharma Division Location: Panoli, Gujarat 1 Position: QC Executive/officers (Total open 10 position) Experience : 2 to 7 Years Expertise Required : Hands-on experience in GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography) Qualification : B.Sc / M.Sc (Chemistry or related field) 2 Position: QC Officer Experience : 2 to 4 Years Expertise Required : Exposure to HPLC/GC/Analytical Techniques Qualification : B.Sc / M.Sc (Chemistry or related field) If you're passionate about pharmaceutical quality and analytical excellence, this is your opportunity to grow with a reputed organization! Apply now Send your CV to: dipika@uppl.in With Warm Regards, Ms. Dipika Gajjar Utkarsh Placement Pvt. Ltd. Vadodara Email: dipika@uppl.in Preferred candidate profile

Responsible for testing of Raw material,IP/ FP and Stability sample as per method of analysis Should have knowledge for the Method Verification/validation and Method Transfer analysis Have an exposure on operation, calibration, Qualification and maintenance of laboratory instruments / equipments. Have an exposure for the preparation of calibration & PM schedule of laboratory instruments / equipments. Should have knowledge for the preparation, handling & management of working/reference standards etc. Testing of In-process, stability and Finished product samples Should have awareness of Caliber LIMS system operation.

Role & responsibilities 1. Responsible for analysis of FG and Raw materials 2. Ensure adherence to GMP & cGMP 3. Maintain and calibrate GC instrument 4. Prepare and review analytical documents and reports Preferred candidate profile B.Sc./M.Sc/ or B.Pharm. Hands on experience in GC operation Familiarity with regulatory audits

Perform a wide range of chemical and physical tests on samples, including pH, titrations, chromatography and other analytical techniques. Preparation and standardization of Volumetric solutions and reagents. Quality Assurance: Ensure that products meet established quality standards and specifications. Maintain instrumentation GLC and flame photometer

To perform analysis on HPLC and Gas Chromatography as per specification and testing method and as per pharmacopeia monograph. Responsible for calibration of HPLC and Gas Chromatography as per schedule calibration of QC instrument. preparing SOPs

We are seeking a dedicated Service Engineer with experience in the pharmaceutical industry to handle installation, commissioning, maintenance, and technical support of our equipment and systems. Your role is critical in ensuring customer satisfaction and compliance with industry standards. Role & responsibilities : Perform installation, commissioning, and preventive maintenance of pharmaceutical machinery and cleanroom systems. Troubleshoot technical issues on-site and remotely, ensuring minimal downtime for clients. Provide technical training and support to customers and internal teams. Maintain service documentation, reports, and customer logs. Ensure all work complies with GMP, safety, and regulatory standards. Preferred candidate profile : - Qualifications Required: BE/BTECH in ( Instrumentation / Electronics and Telecommunication) , BSC (Physics) - 1-6 years of field service experience, preferably in pharmaceutical or healthcare environments. - Familiarity with pharmaceutical equipment such as PLC, SCADA,HVAC systems, cleanroom equipment, isolators, or processing machines (preferred). - Strong problem-solving and customer service skills. - Willingness to travel extensively to client sites. What We Offer: Competitive salary + high-performance incentives Learning & development opportunities Career growth opportunities in a fast-growing sector A collaborative environment with innovative technologies Training and development opportunities How to Apply: If you're passionate about pharma instrumentation and sales leadership, wed love to hear from you! Apply directly via LinkedIn or send your CV to : HR Sonica : Technohr@technovalue.in / 88797 73091 Subject Line: "Application Service Engineer Pharma Instruments"

Role & responsibilities Preferred candidate profile

Job Title: Junior Analyst / Analyst Experience: 1 to 3 years Location: Hyderabad CTC: 2.5 3.5 LPA Qualification: M.Sc. in Chemistry / Analytical Chemistry Preferred profile: from a food testing laboratory background Job Description: We are seeking a dedicated and skilled chemist with 1 to 3 years of experience in HPLC impurity analysis handling within the food testing industry. The ideal candidate should have a strong foundation in analytical chemistry, method development, and instrument calibration. Key Responsibilities: Perform HPLC impurity analysis in accordance with regulatory and laboratory standards. Conduct routine calibration and maintenance of HPLC instruments. Ensure accurate documentation of sample preparation, analysis, and results. Adhere to Good Laboratory Practices (GLP), ISO 17025 standards, and safety protocols. Assist in method development and validation as per standard operating procedures. Maintain and update instrument logs and calibration records to support audit readiness. Collaborate with QA/QC teams to ensure compliance and continuous improvement. To analyze all Food & Agri samples using HPLC as per IS, AOAC, FSSAI , SOP and customer supplied methods. To Calibrate and perform Intermediate checks for all major and minor laboratory instruments such as HPLC, pH meter, micropipette, sonicator etc. To analyze all the food & Agri samples using GC and UV-Visible spectrophotometer as per IS, AOAC, FSSAI and customer supplied methods. To develop, validate and verify methods as per requirement using HPLC & GC. Candidate Requirements: M. Sc - Chemistry. 1 to 3 years of relevant experience in HPLC and GC techniques, preferably in a food testing laboratory. Hands-on experience with chromatographic software and analytical instrumentation. Willingness to work in rotational shifts. Flexibility to relocate to other branches across India including Bangalore, Nellore, Nashik, Mumbai, Ahmedabad, and Noida for deputation or transfers. Strong analytical skills, attention to detail, and effective communication abilities. Regards, Priyanka Jajula Sr. Executive - HR

Role & responsibilities Preferred candidate profile Perks and benefits

Openings for Residue analysis persons in Food Testing - Hyderabad , Navi Mumbai , Ahmedabad Designation : Junior / Senior Analyst Experience: 2- 10 Years Department : Residue Location : Hyderabad Qualification : M.Scs. (Organic Chemistry/Chemistry/Analytical chemistry) Industry : CRO & Testing Laboratory (Third party testing lab ) 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 Products and Miscellaneous samples. Mycotoxin analysis in Food & Agricultural products and feed samples. Use and calibration of instruments such as Micro Pipettes, Analytical Balance, Micro balance, Centrifuge, Turbo Evaporator, HPLC & GC. Analysis of Residue in food by LC MS/MS,GC MS/MS, method development and validation, food additives, contaminants analysis on HPLC,GC with different detectors, Worked in ISO 17025:2017 and FSSAI approved lab NABL audit will be added advantage. Regards, Priyanka Jajula

To perform analysis on HPLC and Gas Chromatography Responsible for preparing SOPs Responsible for calibration of HPLC and Gas Chromatography as per schedule calibration of QC instrument To assist the Head QC in investigation of OOS results.

Ensure that the manufactured products consistently meet established standards, customer specifications, and industry regulations Optimize processes and drive continuous improvement initiatives Product Modification/ Development as per customer need Required Candidate profile B. Sc Chemistry with M. Sc Polymer Science mandatory 12+ years' experience in Quality Assurance & Control in a chemical/ polymer manufacturing company (preferably in polystyrene manufacturing)

QC Testing,HPLC,RP, Stability,GLP

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Responsibilities: Conduct wet analyses and method validations Ensure compliance with industry standards and regulatory requirements Maintain cleanliness and safety protocols in the lab environment Share cvs to ramya_n@hikal.com

Designation - Chemist /Officer / Sr. Officer - QC Company - Leading Chemical Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. Experience - 1yr. to 6yrs. Total Openings - 5 Nos. share with your friends. Required Candidate profile Analysis of RM, PM, IP, FG prepare approved or rejected test report calibration activity for laboratory instrument like - GC, HPLC, IC, Balance, pH Meter, Ion Analyzer, Karl Fischer Total Openings- 5

Core Responsibilities 1. Conducting Chemical Analyses Perform routine and specialized chemical tests on raw materials, in-process samples, and finished products using techniques such as chromatography, spectroscopy, and titration. Analyze organic and inorganic compounds to determine their composition and purity. 2. Preparation of Reagents and Solutions Accurately prepare test solutions, compounds, and reagents by weighing ingredients and dissolving or diluting substances as necessary. Develop nonstandard tests for chemical products to assess their quality and performance. 3. Data Analysis and Reporting Interpret test results, compare them to established specifications, and report findings in a timely manner. Document all test results and maintain accurate records in compliance with regulatory requirements and company policies. 4. Maintenance of Laboratory Equipment Ensure all laboratory instruments and equipment are regularly calibrated, maintained, and in good working order to guarantee accurate results. Troubleshoot and report on malfunctions, and perform routine maintenance as necessary. 5. Compliance with Safety and Quality Standards Ensure compliance with laboratory health and safety guidelines, including the proper handling and disposal of hazardous materials. Follow Good Laboratory Practices (GLP) and adhere to regulatory requirements such as ISO standards to maintain data integrity and laboratory accreditation. 6. Collaboration and Communication Collaborate with other scientists and team members on research projects and quality improvement initiatives. Provide technical support to other departments and assist in problem-solving efforts related to chemical testing and product development.

Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA