962 Gc Jobs

Role & responsibilities Quality Control: Perform High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and various wet chemical analyses to ensure product quality. Analyze raw materials, intermediates, and finished products as per established quality standards. Prepare SOPs in line with regulatory requirements, including stability studies and market sample analysis. Ensure GLP-oriented documentation and maintain accurate records for audits and compliance. Work proficiently on multiple laboratory software platforms to support analytical testing and reporting. Quality Assurance: Ensure cGMP and regulatory compliance across all QA operations. Manage AQA, IPQA, batch release, deviations, CAPA, change control, and audits in line with quality standards. Oversee analytical data review and ensure strict adherence to data integrity principles (ALCOA+). Monitor on-floor QA activities, in-process checks, and documentation for accuracy and compliance. Maintain strong control over qualifications, preventive maintenance, and calibration reviews. Prepare quality documents independently as per regulatory and organizational requirements. Drive automation, digitalization, and continuous improvement initiatives.

We are seeking a highly skilled Executive / Sr. Executive Quality Assurance with 8 to 10 years of experience in API / Bulk Drug Manufacturing . The role involves overseeing laboratory incidents, OOS/OOT investigations, analytical method validations, data integrity compliance , and ensuring adherence to GMP and regulatory standards . Key Responsibilities: Handle and review laboratory incidents, OOS (Out of Specification), OOT (Out of Trend), deviations, and root cause investigations . Review and monitor calibration schedules and records for critical analytical instruments (HPLC, GC, UV, IR, AAS, ICP-MS). Oversee analytical method validation, method transfers, and specification reviews in alignment with regulatory requirements. Provide training to QC teams on laboratory procedures, data integrity , and documentation practices . Conduct surprise lab audits/visits and proactively identify compliance gaps to ensure readiness for inspections. Ensure compliance with cGMP, ICH, and regulatory guidelines throughout QA operations. Eligibility Criteria: Education: B.Sc / M.Sc in Chemistry or related field. Experience: Minimum 8 to 10 years in pharmaceutical Quality Assurance (API / Bulk Drug). Preferred Candidates: Male candidates available for immediate joining .

Responsibilities: (1) To conduct analysis such as GC, HPLC, Wet Chemistry, GC-MS, LC-MS, FTIR, UV-Vis, DSC, Particle Size Analyzer, Viscosity, Density etc.(2) To maintain Analytical Lab note books, procedures, documents and records(3) To maintain laboratory and work place as per norms(4) To maintain ISO 17025 and ISO 9001 management systems(5) To work safely and maintain housekeeping of the lab(6) To work in shifts as per requirement of the job(7) Implement SOP for the storage of analytical standards and reference samples at Thane under required conditions and maintain a database

Monitor progress of the reactions by using standard methods & analytical techniques (TLC,GC,HPLC, LCMS etc).Plan, setup, monitor, and workup chemical reactions independently.Isolate product & Optimize.

Product Development: Assist in the design, formulation, and testing of new products or services, ensuring they meet quality and performance standards.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA

Candidate must have strong knowledge in Core PHP, Laravel, MYSQL, jQuery, AJAX, HTML and CSS. Must have a work experience of 1-2 years on PHP & Laravel Framework. Web-based software application development and maintenance on PHP

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials

1. Coordinate with Sales team and Plant from Order punching to despatch details 2. Regular Follow up for the Payments from clients 3. Support sales team for Quotes, Ledgers, PI, Debtor reports, monthly and weekly sales reports

Planned purchase to maintain stock. Having knowledge in IT Hardware & Software Procurement. Creating PO & Buying Activities. Having a good Knowledge in material Follow-up with Vendor & Supplier.

Key Responsibilities: Strategic Actively imbibing the values and philosophy of PI Industries. Efficient contribution to the overall success of product innovation (PRI) through scientific contribution to objectives and targets being set by the leadership team. Fullfilling requirements and achieveing goals set by the Team Leader and Group Leader Working as a team member, contributing to the team objective with special focus on achiving and exceeding the set target. Development of individual & team strengths by attending trainings based on the regular feedback as an individual and as a team Operational Monitoring reaction masses using LCMS/GCMS. Execution of purity assessment and assay determination of samples using GC/HPLC/UFLC. Able to carry method development for challenging compounds through GC/GCMS/HPLC/UFLC Developing methods on Prep HPLC for purification/isolation of impure compounds. Elucidating and confirming structures using NMR, FTIR and LCMS/MS Ensure the scheduled performance of calibrations, Preventive maintenance and troubleshooting of core analytical instrument. Following the set instrument maintenance practices like periodic solvent changes, system flushing, etc. Assist the other team members in day to day activities like sample preparation, method developments, report generation and data management. Following safety practices with out fail. Financial Planning the activities with existing resources and infra structure. Suggesting the cost-effective areas to the Team Leader / Group Leader Developing methods to improve the environment safety and to reduce the cost. People Collaborate with team members and cross functional teams to meet research objectives. Develop and foster positive relationships with other teams and support groups to maximize cooperation and consequent benefit to objective delivery Should be able to work in multitasking environment Ensure team harmony through collaboration and active participation in all team discussion Apart from the above responibilities, specific responsibilities of Research scientists Note : The Associate would in any of the areas listed below based on the requirement and should have sufficient knowledge and expertise in the area alloted as listed below 1. HPLC/UFLC Candidate should be well versed with normal and reverse phase chromatography techniques. Able to optimize chromatographic methods Keen knowledge on low level analyte-impurities quantification by HPLC. 2. LCMS SQD & TQD Well versed with operations of one or more makes of LCMS-SQD & TQD instruments. Aware of basic principles related to mass spectrometry, sources, analysers and detectors. Hands on experience in analysis of compounds using LCMS instrument and releasing the mass confirmation reports. Keen knowledge on ppb / ppm level quantification of analytes from AI, formulations, various matrices like microsomes, soil, plant extracts by LCMSMS. Perform possible structural elucidation/Identification of degradants/metabolites/impurities using LCMS/MS 3. NMR Perform suitable 1D/2D NMR experiments based on the requirement and confirm one among proposed structures or propose a new structure. Manage the NMR activities viz, perform routine NMR (1D&2D) analysis, QNMR, cryogen replenishing. Keen knowledge of NMR technology & instrument maintenance. 4. Physchem assays Have hands on knowledge of various in vitro ADME/ physchem assays like solubility, LogP, pKa and in vitro Metabolic stability assay. Able to develop methods, check method compatibility for accuracy, precision, matrix effect and apply it further for the quantification of formulations, plant extracts, various matrices like soil, microsomes etc. Perform the microsomal stability experiments to determine half-life and Clint. Awareness about Met ID using various scans, fragmentation tree & HRMS will be an added advantage. Knowledge about sample preparation and analysis of photo stability and hydrolytic stability. 5. Prep-HPLC Able to develop a robust chromatographic method both at analytical and preparative scale, by designing cost effective methods for chiral and achiral molecules. Knowledge of chiral chromatography and isolation of enantiomers using preparative HPLC. Please share updated resume on e-mail id Shubhi.chandnani@piind.com Mobile - 8875001305

analytical lifecycle: specs with RA, method validation, testing of RM/PM/IP/FP, water & environmental monitoring, stability programs.data integrity (ALCOA+), LIMS audit trails chromatography governance (integration, SST, system suitability).

ONLY FOR MALE CANDIDATES ROLES: Executives and chemists SALARY: 2 lpa to 6.5 lpa Please carry last 3 months pay slips,6 months bank statements,CTC details and updated CV. Desired Candidate Profile * Conduct quality control tests on bulk drugs using HPLC, GC, and other relevant methods. * Develop and implement quality assurance procedures for API manufacturing processes. * 2-7 years of experience in API production or related field. * Proficiency in HPLC, GC, and other analytical techniques for testing bulk drugs. * Experience with QA management systems and implementation of quality control procedures.

Role & responsibilities Sample testing Documentation equipment calibration Preferred candidate profile Qualification -MSc in chemistry is must . Must have experience in Pharma - API industry or Testing laboratory . Must be have having good experience in HPLC , GC ,Wet analysis , Stability , Finished products ,Raw - Material .

Role & responsibilities : Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP . Analytical skill for QC instrument, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc. Regularize the QC activities as per cGMP requirements. RM, PKG, In-process and FG sampling & Analysis. Co-ordination with QC staff, R&D, Commercial and production for quality & dispatch related activities for on time dispatches. Day to day monitoring and execution online all IPQC and FG analysis activities. Resolve the trouble shooting related to QC activities. Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11) Awareness about responsible care (Environment, Health, Safety and Security)

JD: 1. To assist in implementing and maintaining quality management system. 2. Conducting audits and inspections, analysing quality data and ensuring compliance with regulatory standard. 3. Including leading QC teams, overseeing raw materials and and finished products. 4. Managing corrective actions, preparing reports and driving continuous improvement process quality. 5. Regular internal QC inspection to assess complies and identify quality issues and pinpoint areas for improvement. 6. Manage and guide quality control analysts and technicians, providing training and support to ensure team performance. 7. Work closely with cross-functional teams, including production and engineering, to resolve quality-related problems and implement preventive measures. 8. To maintain accurate records of quality control activities, including inspection reports, test results, and audit findings. 9. To implement and enforce quality control policies and procedures to ensure adherence to internal standards, regulatory requirements (e.g., FDA, ISO), and industry best practices.

Role Overview: As a QC Team Leader at our company located in Ambernath, Maharashtra, your primary responsibility will be to lead a team of 30+ members in the QC-AMV team, including LC-MS, Nasal, and FT-NIR teams, for regular testing and method validation activities. You will also provide backup support to the QC Head of Department (HOD) by managing daily updates, commercial output, monthly sample status, training, review meetings, and coordination with stakeholders to align work requirements. Your role will involve executing and approving various types of Quality Management System (QMS) processes, identifying scientific root causes, implementing corrective and preventive actions (CAPA), and ensuring laboratory compliance. Key Responsibilities: - Lead the QC-AMV team for regular testing and method validation activities with analytical knowledge and leadership qualities to achieve company goals. - Support the QC HOD with daily updates, commercial output, monthly sample status, training, review meetings, and stakeholder coordination. - Execute and approve different QMS processes, identify root causes, implement CAPA, and maintain lab compliance. - Design and execute analysis planning, data interpretation, and presentation to the HOD. - Provide guidance to team members, monitor key performance indicators, and lead QC-AMV work in the absence of the QC HOD. - Collaborate with cross-functional teams, stay updated on industry trends, and ensure compliance with GLP and health, safety, environmental systems. - Manage work in all shifts and travel to other sites as per company policy. Qualifications Required: - Master's degree in Science or Bachelor's/Master's in Pharma. - Strong analytical knowledge and expertise in modern analytical instruments (HPLC, GC, LC-MS, NIR, Nasal performance testing). - Work experience in QC, AMV, and AD departments. - Leadership skills, problem-solving abilities, strategic mindset, organizational skills. - Knowledge of Chromeleon 7.2 and Sciex software is advantageous. - Experience in GMP, USFDA/EU audits. - Excellent communication skills. (Note: Additional details about the company were not included in the provided job description.),

Role Overview: As a Chemist in the Instrumentation Laboratory (Residue Lab), you will be responsible for the preparation and analysis of samples using various Instrument techniques while ensuring strict adherence to safety and documentation protocols. Your role will involve receiving, handling, and storing samples and standards, conducting analysis on instruments in compliance with regulations, and contributing to method development and validation. Strong analytical skills and knowledge of NABL and ISO/IEC 17025:2017 standards are essential for this role. Key Responsibilities: - Sample Preparation & Analysis: - Receive, handle, and store samples - Prepare samples, conduct analysis, and generate reports - Prepare chemicals, reagents, diluents, and standardization solutions - Instrument Operation & Maintenance: - Operate instruments such as HPLC, GC, LC-MS/MS, GC-MS/MS, or ICP-MS for residue analysis - Interpret analytical data and troubleshoot technical issues - Perform testing according to specified methods and standards - Calibration & Intermediate check of Instruments: - Maintain records for verifications, intermediate checks, and preventive maintenance - Monitor cylinder maintenance - Method Development & Validation: - Develop, validate, and verify methods - Prepare SOPs and STPs - Handle certified reference materials - Data Management & Indent: - Process raw data, perform calculations, and generate analytical reports - Maintain records in compliance with GLP and ISO 17025 requirements - Collaborate with other departments and chemists - Compliance & Quality Control: - Participate in ILC, IQC, and Professional testing - Follow GLP, 5S, and safety guidelines - Ensure analysis compliance with regulatory standards - Safety & Housekeeping: - Adhere to lab safety protocols and waste disposal procedures - Maintain cleanliness and orderliness in the laboratory - Team Collaboration & Learning: - Work under supervision and participate in training sessions - Stay updated with new analytical methods and technologies - Coordinate with team members and report any deviations promptly Qualification Required: - Post Graduation/B.Tech in Food Technology/Chemistry/Bio Technology or Equivalent - 2-5 years of experience in an NABL Food testing laboratory - Knowledge of NABL, ISO/IEC 17025:2017 standards/rules regulations - Analytical mindset with attention to detail Working Conditions or Location: On-Site at Sangariya Fanta, Jodhpur, Rajasthan (Note: Any additional details of the company were not included in the provided job description.),

Definedge Securities Broking is looking for Core Java Developer to join our dynamic team and embark on a rewarding career journey ResponsibilitiesDesign, develop, and maintain high-quality applications, taking full, end-to-end ownership, including writing test cases, setting up monitoring, etc Participate in code reviews and provide constructive feedback Make sure that application code coverage meets our minimum levelSkillsStrong in object-oriented design principles and functional programming In-depth knowledge of the Java concurrency framework is a must A very strong command of data structures and algorithms, plus how the Java collections framework uses them Sound knowledge of concepts like exception handling, garbage collection, and generics Experience in writing JUnit test cases, using any framework like Mockito, PowerMockito, EasyMock, etc Hands-on experience with lambdas and streams is a must Good command over any well-known IDE like IntelliJ, Eclipse, NetBeans, etc Experience in using build tools like Maven and Ant Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Officer Quality Control - API & Intermediates Education - M.SC - Analytical / Organic Experience 1 to 3 years experience in Quality Control from pharmaceutical industry. (This is a Fixed Term Contract role - On Company's Contract) Job Description - Sampling of raw, packing material, intermediate & finished product. Analysis of raw, packing material, intermediate, stability samples & finished product. Analysis of process & cleaning validation samples. Preparation of standard volumetric solution, reagent & standardization of volumetric solution and check for stability. Inventory of Instruments Spares, Chemicals & Glassware. To maintain cleanliness, personal and environmental safety & follow Good Laboratory Practices during work. Ensure environment protection by controlling Air / Water / Soil pollution from analytical activities. Accountable for the safe operation of the facility, their own safety and safety of other co- workers. Technical & Behavioral Competencies - • Instrumentation & Analysis in Quality Control • Aware of GXP requirement in Quality Control Laboratory, Data Integrity & ALCOA+ • Knowledge of laboratory investigation • Good Communication Skills, team player, collaboration. • Knowledge of MS Office - MS Word, Excel

About the Team At Nutanix Cloud Manager, we are trying to build the next generation platform to help enterprises model, develop and manage applications. We want to give them the ability to encapsulate not only infrastructure but even the application its architecture and deployment as code. You will be reporting to the Senior Manager Engineering, QA - NCM Team. Your Role As the gatekeeper of our product quality, you would be required to ensure that product releases adhere to the highest quality norms. You will design and develop a testing framework for our products and be part of a ruthless quality team. You will develop test tools, test cases, maintain test beds, and provide metrics and test/quality status. What You Will Bring: Be a self-starter who can flourish in a fast-paced technology company Be the owner of our automation and delivery systems Be actively participating in Coding & Code reviews Have expertise in languages like Python, JAVA Have expertise with automation and building tools such as Selenium, JMeter and Jenkins Strong systems background (Linux systems with exposure to Process, Memory and IO Management tools You will enable our engineers to generate known-quality releases with every commit, discover defects early and iterate fast. Thrive on working on open-source technologies. Excellent programming and scripting capabilities to develop code for automated tests. Should have an extremely good problem-solving approach with good hands-on knowledge of Algorithms & Data Structures.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC

Design and execute laboratory synthesis of organic/inorganic compounds according to project requirements. Develop and optimize synthetic routes to improve yield,purity.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation