80 Gc Analysis Jobs

Job Description Value added Service [Acceptance Solutions]is a Product Development (PD) Group within the Team. This group is responsible for building leading edge full-service Payment Solutions for our customers by combining global payment processing, fraud management, payment security and reporting systems. We are a group of bright, motivated engineers and technical managers excited about building the next generation of Payment products that will drive e-Commerce, mobile-Commerce as well as POS businesses for our customers. Accountable for creating application and infrastructure performance plans/models for a highly scalable, low-latency, highly-available and high-throughput payment process...

Knowledge in Handling of HPLC and GC . Analysis results review and supported to team work. Competencies Result Orientation Breakthrough Achievement Speed Agility Exceptional Achievement Service Delivery Excellence Exceptional Achievement Teamwork Collaboration Breakthrough Achievement Business Knowledge Breakthrough Achievement Qualification Groups Graduation B.Sc Post Graduation M.Sc Post Graduation M.Pharma Graduation B.Pharma

Roles and Responsibilities Perform GC analysis of samples using various instruments such as GC-MS, GC-FID, and GC-TCD. Conduct quality control tests on standards and samples to ensure accuracy and reliability of results. Develop and maintain calibration protocols for GC instruments to ensure optimal performance. Collaborate with cross-functional teams to resolve issues related to sample preparation, instrument maintenance, and data interpretation. Ensure compliance with regulatory requirements by maintaining accurate records of test results, standard preparation, and instrument calibration. Desired Candidate Profile 2-6 years of experience in a pharmaceutical industry setting with expertise ...

Role & responsibilities Job Summary: We are seeking a detail-oriented and experienced Analytical R&D Chemist to join our synthesis lab. The ideal candidate will be responsible for developing, validating, and implementing analytical methods to support the research and development of new chemical entities and active pharmaceutical ingredients (APIs). This role requires a deep understanding of analytical chemistry, instrumental analysis, and method development. The Analytical R&D Chemist will collaborate with cross-functional teams to ensure the accuracy and reliability of analytical data. Key Responsibilities: Method Development and Validation: Develop and validate robust analytical methods fo...

Role & responsibilities Managing the day-to-day operation of the concerned department in a complying and in safe manner. Preparing and issuing the job descriptions to the concerned team member. To ensure that only current and authorized documents are being used in the department. Verification of log books and raw data. Verifying the accuracy and validity of technical data, ensuring its proper recording and archiving. Review of method development, verification, validation, protocols, reports and raw data. Supervise and participate in developing, validating, and transferring analytical methods for drug product testing. Ensure all testing procedures comply with established protocols, maintainin...

As an SRE Lead / Performance Engineer in the banking sector, your role will involve monitoring critical banking applications, analyzing issues, and providing performance tuning recommendations to ensure stability, scalability, and high availability of core and digital banking platforms. - Lead production performance monitoring and incident analysis for core and digital banking applications. - Monitor transaction performance, system health, and SLAs using APM and observability tools such as Dynatrace, AppDynamics, Grafana, Prometheus, Splunk, and ELK. - Perform root cause analysis (RCA) for performance issues, including application slowdowns, DB query bottlenecks, GC pauses, or infrastructure...

Responsibilities: * Conduct HPLC, GC & UV analyses under supervision. * Maintain quality control procedures and documentation. * Ensure compliance with industry standards. Health insurance

Job Overview: A Tech support Engineer is responsible for the availability, performance, monitoring, and incident response, among other things, of the platforms and services that our company runs and owns. We must make sure that everything that goes to production complies with a set of general requirements like diagrams, dependencies of other services, monitoring and logging plans, backups, and possible high availability setups. Even when the software complies with all the necessary requirements such as uncaught exceptions, hardware degradation, networking problems, latencies, high usage of resources, or slow responses from our services could happen at any time. We always need to be prepared ...

Job description Roles and Responsibilities Conduct analytical testing using HPLC, GC, UV-Vis, ICP-MS, LCMS techniques to ensure product quality and purity. Develop and validate methods for analysis of pharmaceutical products according to cGMP guidelines. Collaborate with cross-functional teams to resolve method validation issues and implement changes as needed. Maintain accurate records of test results, instrument calibration, and maintenance schedules. Participate in continuous improvement initiatives to optimize laboratory processes and procedures.

Role & responsibilities * Instrumental analysis i.e. GC, HPLC, UPCL, PH meter. * Chromatographic analysis of raw material, finish products, intermediates. * Knowledge about Empower 3 software * Follow good laboratory practices (GLP) in quality control department. * To prepare the COA of API & intermediate material

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (02 07 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ Micro-biology ARD - OSD Experience: (02 06 Years) •HPLC/ FG/Analytical Method validation/ Stability PACKING Experience: (01-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer & Jr.Executive NOTE: Offering a Joining bonus only for QC Depart. for Immediate Joiners Instrument experience in HPLC / GC ...

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/...

We atre looking the below positions for our Group of Companies which are located in Hyderabad QC EXECUTIVES -12 OPENINGS Role & responsibilities Handling Of the stability study. Experience in Wet Analysis and HPLC, GC Instrumentation. Communicate effectively with cross-functional teams,including production,R&D, Preferred candidate profile Minimum 1 -5 years experience In Quality Control Must Have BSC/MSC-Chemistry/B.Pharmacy/M.Pharmacy Salary no bar to right candidates. one male candidates R&D EXECUTIVES -6 OPENINGS Develop and optimize processes for Chemical/ (API) manufacturing, ensuring efficiency and cost-effectiveness. Develop new chemical processes Conduct literature research, experime...

We atre looking the below positions for our Group of Companies which are located in Hyderabad QC EXECUTIVES -12 OPENINGS Role & responsibilities Handling Of the stability study. Experience in Wet Analysis and HPLC, GC Instrumentation. Communicate effectively with cross-functional teams,including production,R&D, Preferred candidate profile Minimum 0 -5 years experience In Quality Control Must Have BSC/MSC-Chemistry/B.Pharmacy/M.Pharmacy Salary no bar to right candidates. one male candidates R&D EXECUTIVES -6 OPENINGS Develop and optimize processes for Chemical/ (API) manufacturing, ensuring efficiency and cost-effectiveness. Develop new chemical processes Conduct literature research, experime...

Testing of incoming raw material Standardization of Solution Testing of in process tests samples Testing of Finished Product as per Specification Qualification (IQ, OQ, PQ) and Calibration of QC instruments Preservation and Disposal of Samples safe work practices and Good Housekeeping in the Laboratory. Preparation of Purchase Indent of Glasswares, Chemicals and other Auxiliaries. Internal Communication with Production, Marketing and concerned Department. ERP entry work Preparation of SOP, protocols and other documents. Knowledge of 21 CFR part 11

As an experienced candidate with 4+ years of experience, holding a B.E/B.Tech in Computer Science or Information Technology, or MCA (full-time), without distance learning, you are required to have expertise in Oracle DB and WebLogic. The role is based in Delhi and involves rotational shifts. **Responsibilities:** - WebLogic Installation, Upgrade & Patch Management: You must be capable of installing WebLogic, performing upgrades, and applying critical/security patches across environments. - Performance Tuning & Optimization: Your role will include tuning JVM, Work Managers, thread pools, and other WebLogic parameters for optimal performance. - JMS (Java Messaging Service) & Queues Management:...

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...

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

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.

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

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/...

Oversee daily nutraceutical juice production, ensure GMP/FSSAI compliance, maintain quality checks, manage equipment & manpower, and support new product trials. To apply, contact: 9571213413 Required Candidate profile Experienced nutraceutical production chemist with 2–7 years’ expertise in juice processing, GMP compliance, and quality control. Skilled in formulation, blending, and batch documentation.

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/...

Good Background in chemistry Hands on experience in product development Communication & teamwork skill Exposure to Scale up process chemical analysis techniques like HPLC, GC, along with wet analysis like titration etc. 2 to 5 years of experience in R&D - Synthesis & ADL.