65 Gc Analysis Jobs - Page 2

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, c...

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...

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...

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/...

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 ...

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 Man...

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 Requiremen...

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...

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

Roles and Responsibilities Conduct quality control analysis of bulk drugs, APIs, and finished products using GC, HPLC, and other relevant techniques. Develop and maintain SOPs for laboratory operations, sampling procedures, and testing protocols. Ensure timely reporting of test results and maintain accurate records.

Job Description: We are hiring a Quality Control Executive for our API manufacturing unit. The ideal candidate must have hands-on experience in HPLC/GC , a sound understanding of GMP/GLP , and should be able to manage end-to-end QC activities as per regulatory and organizational requirements. Key Responsibilities: Sampling of raw materials, packaging materials, water, in-process samples, validation samples, stability samples, finished products, process aids , and equipment cleaning samples . Perform analysis of samples using appropriate techniques and instruments (HPLC/GC), based on qualification and training. Perform upkeep and calibration of laboratory instruments and equipment . Responsib...

The role involves handling the following responsibilities: Monitoring of Wet Analysis Specification Preparation CCF Handling Instrumentation: HPLC and GC Analysis

In this role, you will: Lead moderately complex initiatives and deliverables within technical domain environments Contribute to large scale planning of strategies Design, code, test, debug, and document for projects and programs associated with technology domain, including upgrades and deployments Review moderately complex technical challenges that require an in-depth evaluation of technologies and procedures Resolve moderately complex issues and lead a team to meet existing client needs or potential new clients needs while leveraging solid understanding of the function, policies, procedures, or compliance requirements Collaborate and consult with peers, colleagues, and mid-level managers to...

Role & responsibilities Aurobindo Pharma Ltd. Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Assurance (Market Complaints / QMS / Validation / IPQA) Quality Control (GMP / GC / LCMS / HPLC) 3 Experience Required: 2 7 years (pharmaceutical manufacturing) Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Quality Assurance Key Scope • Handle Market Complaint investigations, trend analysis and regulatory responses • Maintain site QMS: Deviations, CAPA, Change Control, Audit readiness • Execute and review Equipment / Process / Cleaning Validation documentation • Perform IPQA activities: line clearance, in-process checks, batch recor...

Role & responsibilities Knowledge of Polymer testing ,raw material testing ,in-process testing, utility samples -water, steam and ETP water testing and general chemical testing, instrument handling: GC,UV,KF,AUTO Titrator, Moisture balance, flame photometer and etc. Essential: above 2-3 years Desirable: Qc lab working experience of chemical industry

"Quality Control Chemist wanted. Conduct analytical tests (HPLC, GC, wet analysis), ensure product quality, and adhere to regulatory standards. Analyze data, follow SOPs, and maintain accurate records."