60 Aqa Jobs

Issuance of Analytical Data Sheets and Formats. Preparation and Review of specification and standard test procedure. Review of QC Analytical Data. To ensure online documentation in laboratory as Good Documentation Practices. To attend training as per refresher training schedule. To ensure all time audit readiness in the work area. To perform any other work as and when assigned by Head of department.

Role & responsibilities 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. Preferred candidate profile M.Sc. Organic Chemi...

Senior Officer QA (QMS) 1 Post based in Kathua, Jammu & Kashmir. The ideal candidate brings 4 - 6 yrs exp 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...

Senior Officer QA 3 Posts based in Kathua, Jammu & Kashmir. The ideal candidate brings 4-6 yrs exp 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...

Quality Assurance Pharmacovigilance (PV) Specialist based in Hyderabad. The ideal candidate brings 3-5 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/Ka...

Senior Executive QA 1 Post based in Kathua, Jammu & Kashmir The ideal candidate brings 8-10 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) S...

Issuance of Analytical Data Sheets and Formats. Preparation and Review of specification and standard test procedure. Review of QC Analytical Data. To ensure online documentation in laboratory as Good Documentation Practices. To attend training as per refresher training schedule. To ensure all time audit readiness in the work area. To perform any other work as and when assigned by Head of department.

Should have strong knowledge in all analytical techniques like HPLC, GC and chemical analysis Should have strong knowledge or skill in Analytical method validation and Cleaning method validation Should have strong knowledge in Audit trial reviews in analytical techniques Chromatography and chemical analysis Should have knowledge in Empower software CDS Should have knowledge in standards management like ( Reference standard / working standard) Should have knowledge in Stability analysis, Forced degradations analysis and its review Should have knowledge in review of all analytical raw data. Should have knowledge in Data Integrity and 21 CFT part 11 compliance Should involved in regulatory audi...

Senior Officer QA (QMS) 1 Post based in Kathua, Jammu & Kashmir. The ideal candidate brings 4 - 6 yrs exp 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...

Senior Officer QA 3 Posts based in Kathua, Jammu & Kashmir. The ideal candidate brings 4-6 yrs exp 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...

Quality Assurance Pharmacovigilance (PV) Specialist based in Hyderabad. The ideal candidate brings 3-5 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/Ka...

Senior Executive QA 1 Post based in Kathua, Jammu & Kashmir The ideal candidate brings 8-10 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) S...

About the Role We are seeking an experienced Mathematics and Further Mathematics Tutor to support high-achieving students from the UK who are preparing for IGCSE/GCSE and A-Level/Further Maths examinations across exam boards (Edexcel, Cambridge International, AQA, OCR/MEI). The tutor will deliver structured, exam-backward lessons focused on concept mastery, problem-solving, and exam technique, with a track record of guiding students toward top grades (89 at IGCSE/GCSE and A*/A at A-Level). Responsibilities Deliver high-quality 1:1 or small group lessons in Maths and Further Maths. Adapt teaching to different UK exam boards (Edexcel, CAIE, AQA, OCR/MEI). Provide structured lesson plans, homew...

Senior Officer QA (QMS) 1 Post based in Kathua, Jammu & Kashmir. The ideal candidate brings 4 - 6 yrs exp 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...

Senior Officer QA 3 Posts based in Kathua, Jammu & Kashmir. The ideal candidate brings 4-6 yrs exp 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...

Quality Assurance Pharmacovigilance (PV) Specialist based in Hyderabad. The ideal candidate brings 3-5 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/Ka...

Senior Executive QA 1 Post based in Kathua, Jammu & Kashmir The ideal candidate brings 8-10 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) S...

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...

Key Responsibilities: Manage all Analytical Quality Assurance (AQA) activities. Review, approve, and close Quality Management System documents related to QC. Act as Single Point of Contact (SPOC) for submission activities Dossier, Regulatory, Variation filings. Handle customer communications related to QA. Review manufacturing, packing, analytical reports of submission/validation batches. Review Stability data and ensure submission compliance. Ensure compliance of Stability Studies and Control Sample Handling at site. Ensure adherence to GDP/GLP. Monitor compliance of Gowning/De-gowning in QC lab. Authorize written procedures, amendments, and related documentation. Ensure SOP compliance acro...

Issue of documents like raw data, log books and calibration records Review of daily calibration raw data related to QC instruments Distribution and retrieval of standard o[operating procedures Issuance, retrieval of specifications and test methods Review of specifications, Test methods, Qualification documents, Stability/ holding time data protocols, Analytical data. Review of Water system related documents Verifying the raw materials inward and issue registers Initiation of Deviation, CAPA and Change Control Review of Audit Trail for QC Related Instruments Review of Analytical raw data, Calibrations, Daily & Monthly Verifications

Ensure GLP,GDP, STPs, SOPs & SOIs. Calibrate & maintain HPLC, Rheometer, Viscometer, balances. Perform analytical methods and Q3/PEQ characterization studies. Protocols,reports,reagents,routine analysis, PSD, rheology, viscosity, and related studies.

Job Title: AQA Quality Assurance (LCMS, GCMS, ICPMS) Company: Energon Labs Location: Hyderabad Experience Required: 2 - 6 years Employment Type: Full Time, Permanent Role Overview We are seeking experienced professionals in Analytical Quality Assurance (AQA) to review and ensure compliance in analytical data generated through LCMS, GCMS, and ICPMS techniques. The role requires a keen eye for detail, strong knowledge of analytical methods, and the ability to uphold the highest quality standards. Key Responsibilities Review analytical data for LCMS, GCMS, and ICPMS techniques. Conduct electronic audit trail reviews for analytical instruments and ensure compliance. Review Analytical Method Vali...

Issue of documents like raw data, log books and calibration records Review of daily calibration raw data related to QC instruments Distribution and retrieval of standard o[operating procedures Issuance, retrieval of specifications and test methods Review of specifications, Test methods, Qualification documents, Stability/ holding time data protocols, Analytical data. Review of Water system related documents Verifying the raw materials inward and issue registers Initiation of Deviation, CAPA and Change Control Review of Audit Trail for QC Related Instruments Review of Analytical raw data, Calibrations, Daily & Monthly Verifications

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...