47 Gc Analysis Jobs

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.

As an Officer/Senior Officer in the Quality Control department located in Kandla, you will be responsible for handling troubleshooting of HPLC and GC analysis using Chromeleon Software. Your primary task will be to ensure that all work is carried out in compliance with SOP/STP/CSOP/GTP, including adhering to GLP and EHS norms, while maintaining laboratory discipline. It will be your duty to review and maintain all related log books and wet Laboratory records in a timely manner. Your role will also involve overseeing the completion of daily activities and targets, managing HPLC columns, and handling software such as LIMS, LMS, IMS, and SCM. You will be expected to identify gaps in SOPs, analytical worksheets, STP, GTP, etc., and take the necessary steps to update the relevant documents. Additionally, you will be responsible for maintaining all QC SOPs in the display copy, performing calibration activities for all QC instruments as per the schedule, and ensuring the upkeep of the GLP working area. Furthermore, you will be required to conduct and maintain the calibration of HPLC, monitor column management, and analyze in-process, finished product, and stability samples using the HPLC instrument. The ideal candidate for this role should possess a BSC/B Pharma qualification with 4-6 years of experience, preferably from the pharmaceutical industry. If you are detail-oriented, proactive, and have a strong background in quality control, we encourage you to apply for this position and contribute to our team's success.,

The Chemist GC Analysis is responsible for performing GC analysis and documenting the same in compliance with cGMP, cGLP, EHS requirements, and defined operating procedures. You will be required to properly take over shift operations as per defined procedures as a reliever. In terms of GC Systems & Analysis, you will need to go through requisite procedures, plan and prioritize activities based on the work plan received from the supervisor. It is essential to ensure Cylinder status and GC column fixation and stabilization before starting the analysis. Additionally, you will be responsible for the preparation of system suitability solutions, standard solutions, and test solutions as defined in the procedures. Calibration of GC Equipment, evaluation of system suitability, and submission of chromatographs for review are also part of your responsibilities. You must adhere 100% to cGMP and cGLP practices in line with 21 CFR Part 11 and EHS requirements applicable to the QC laboratory. Timely reporting of abnormalities/deviations to the immediate supervisor/appropriate authorities is crucial. Regarding GC Documentation, you are required to record raw data related to system suitability solutions, standard solutions, test solutions, analytical and calibration results. Live recording of each activity, including instrument logbook, column usage log, working standard/reference standard/impurities reconciliation, is essential. Handing over completed documents to the reviewer/ongoing documents to the reliever is also part of your duties. In terms of GC Maintenance, troubleshooting day-to-day issues with respect to instruments with the support of an in-house service engineer is important. Successful completion of assigned trainings and application of the same at the workplace is also required. The minimum educational requirement for this role is a B.Sc. in Chemistry, while a preferred qualification is an M.Sc. in Chemistry. A minimum of 2 years of hands-on experience on Software and Instruments (Make n Model) is required, with a preference for 4 years of experience. The candidate should be aware of quality systems, regulatory and cGMP guidelines, and EHS requirements in Pharmaceutical API companies. Competency requirements for this role include functional knowledge on Software and Instruments, analytical thinking, quality focus, and trouble-shooting skills. Behavioral competencies required are attention to detail, proactive attitude, and problem-solving skills.,

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

IITR is currently looking for a highly skilled ADL Officer for one of the pharmaceutical Co. Location - Vapi, Gujarat. If you are interested and for further information, please share your updated CV to talent@hireindians.com/call on 8700944544. Required Candidate profile Min Exp - 2-4 yrs of experience. Qualification - BSc/MSc in pharma

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.

The role in Pharma Solution's Quality Control department based in Lexington requires you to perform complex testing of raw materials, in-process and finished products while ensuring the calibration and maintenance of analytical instruments in compliance with cGMP standards. This night shift position directly reports to the AQC Group Lead. Your key responsibilities will include conducting routine/non-routine testing using wet chemistry and instrumental analysis methods, testing various samples such as raw materials, APIs, finished products, stability samples, and cleaning verification samples. Proficiency in HPLC/GC analysis is essential along with documenting laboratory work following GDP, cGMPs, and SOPs. Troubleshooting, calibrating, and maintaining instruments, preparing laboratory reagents, and writing SOPs and reports are also part of your duties. You will be required to initiate and resolve laboratory investigations, train entry-level QC personnel, and ensure compliance with safety procedures and regulations. To qualify for this role, you should hold a Bachelor of Science in Chemistry, Pharmaceutical Science, or a related field, with a minimum of 3+ years of hands-on experience in quality control within a laboratory setting. Proficiency in HPLC/GC analysis, previous experience working with cGMP guidelines, and familiarity with potent materials and parenteral drug products are preferred. You must demonstrate a high level of proficiency in operating Microsoft Office applications, possess excellent communication skills, attention to detail, and organizational abilities. Being able to work effectively in a team environment, along with problem-solving and interpersonal skills, is crucial. Following written instructions and maintaining an organized laboratory are key aspects of this role. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions for drug development and manufacturing. The company operates globally with facilities in North America, Europe, and Asia, offering services including drug discovery, pharmaceutical development, clinical trial supplies, and commercial API supply. PPS specializes in highly potent APIs, antibody-drug conjugations, sterile fill/finish, and biologic development and manufacturing services. This is a full-time position with job identification 7804 in the Analytical QC category, posted on 02/26/2025. The location is 1500 BULL LEA ROAD, Lexington, KY, 40511, US.,

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.

Perform routine/non-routine analysis of raw, in-process & finished products using HPLC, GC & other techniques. Maintain accurate documentation as per GLP and ensure strong reporting skills through logs, test reports & records.

Instrument Analysis GC/HPLC for QC department Min 2-5 only API CO 1 to 3 year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

Role & responsibilities: Perform routine and non-routine analysis using GC and GC-MS as per SOPs and approved test methods. Prepare samples, reagents, and calibration standards accurately. Conduct method validation, system suitability, and performance checks for GC instruments. Maintain proper documentation of all analytical results in accordance with GMP/GLP requirements. Troubleshoot analytical issues and assist in resolving deviations and OOS (Out of Specification) results. Ensure proper calibration, maintenance, and operation of GC instruments. Support development and validation of new methods as required by R&D or Quality Assurance teams. Maintain a clean, organized, and safe laboratory environment.

Sr. Executive / Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5-8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Additional info: Key Skills: HPLC, GC Analysis, Method Validation, Wet Analysis, Water Sampling, Report Compilation Qualification: M.Pharm / B.Pharm / M.Sc Experience: 5 to 8 years Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment. Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus.

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 )

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.,

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

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control Experience: (01 12Years) HPLC/ Stability/ GC/ IP/ FP/ RM/ Validation/ Reviewer QUALIFICATION : B.Sc, M.Sc, B. Pharm and M.Pharm with relevant experience DESIGNATIONS: Officer, Jr.Executive, Executive, Sr.Executive & Asst. Manager INTERVIEW VENUE: Hotel: RAUNAK Restaurant Ground Floor, Opp. Axis Bank, Bitna Road, Kalka Shimla National Highway, Pinjore, Haryana 134102 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates Experience in HPLC - Formulation is Mandate Preferred for Male Candidates Share with your friends, collegues and in known groups for better reach CONTACT INFO: E-mail: Harishwar.M@hetero.com & Contact: 8121005416, 9218677050 for further info

Sampling and Inspection of received goods in stores, observation to be maintain. Operation, calibration and record maintained of Q.C Instruments Handling of sophisticated instruments (like GC, HPLC, UV.etc)

Responsibilities: * Oversee gas chromatography, Karl Fischer titration, GC analysis, report preparation, lab testing, and lab operations * Manage lab operations & distillation processes

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control (GMP / GC / LCMS / HPLC) Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits Common Requirements: Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry or related) Sound knowledge of current GMP guidelines (US-FDA, MHRA, EU, WHO) Good documentation, investigation and communication skills Willingness to work in shifts and collaborate with cross-functional teams How to Apply Subject Line: Immediate Joiner Send you updated resume : naidupetahr@aurobindo.com

Instrument Analysis GC/HPLC for QC department Min 2-5 only API CO 1 to 3 year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

Roles and Responsibilities Conduct quality control analysis using GC, HPLC, and other analytical methods to ensure compliance with regulatory requirements. Develop and maintain calibration protocols for laboratory instruments to ensure accuracy and precision of test results. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Ensure adherence to cGMP guidelines and regulations in the pharmaceutical industry. Perform routine maintenance tasks on laboratory equipment to prevent downtime and ensure optimal performance. Desired Candidate Profile 2-4 years of experience in a similar role within the pharmaceutical or life sciences industry. Bachelor's degree in Chemistry (B.Sc) or Master's degree (MS/M.Sc(Science)) from a recognized university. Strong understanding of analytical method development, validation, and implementation principles. Proficiency in operating various types of chromatography systems such as GC, HPLC etc.

3 to 6 years Food testing experience NABL accreditation (ISO-17025:2017) compliance Aware of FSSAI / APEDA / EIC / IOPEPC regulatory requirement Strong analytical analysis of Fatty acid profile, Vitamin & Aflatoxins analysis using HPLC & GC equipment