78 Aqa Jobs

Review all Quality Control data (both electronic and hard copy) related to Finished Products (FP), Raw Materials (RM), intermediates, in-process samples, and stability studies. Review all Chromatographic Data System (CDS) and Non-CDS data, including both electronic and hard copy documents Review Quality Management System (QMS) records and verify closure status of OOS , OOT , laboratory incidents, and all QMS elements related to FP docket

NATCO Pharma is hiring! Join us for a walk-in interview on 06th December 2025 in Chennai across key functions: Maintenance, Production, EHS, QA, QC & Microbiology. Be part of a team that is committed to quality, innovation, and excellence in API manufacturing. Job Requirements Maintenance - Utilities / Mechanical / Electrical / Instrumentation Qualification: DME / B.E (Mechanical / Electrical / Instrumentation ) Operator: 3 to 5 yrs (Utilities Water Systems, AHUs, Compressors, Chillers, Boilers) Supervisor: 7 to 10 yrs (Process & Utility Equipment Maintenance, GMP Documentation) Instrumentation Operator: 2 to 3 yrs (Calibration, Automation) Electrical Operator: 3 to 5 yrs (HT/LT Operation, G...

Walk In Drive Quality Assurance Department In Formulation Division @ Elite Hotel ( MANJEERA HOTELS AND RESORTS) Department :- Quality Assurance OSD Qualification :- B Pharmacy | M Pharmacy | MSC Chemistry Experience :- 2 to 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- Elite Hotel ( MANJEERA HOTELS AND RESORTS) NH 44, Hyderabad - Bangalore Highway, Jadcherla, Macharam, Telangana 509301 Contact No:- 040-30438701 | 070970 92829 | Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those who have expe...

Walk In Drive Quality Assurance Sterile Department In Formulation Division @ Elite Hotel ( MANJEERA HOTELS AND RESORTS) Department :- Quality Assurance Sterile Qualification :- B Pharmacy | M Pharmacy | MSC Chemistry Experience :- 2 to 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- Elite Hotel ( MANJEERA HOTELS AND RESORTS) NH 44, Hyderabad - Bangalore Highway, Jadcherla, Macharam, Telangana 509301 Contact No:- 040-30438701 | 070970 92829 | Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those w...

Role & responsibilities Preferred candidate profile

Walk In Drive For Quality Assurance Sterile In Formulation Division - Kothur Department:- Quality Assurance Sterile Formulations Qualification :- B Sc | B Pharmacy | M Pharmacy| M.sc Experience :- 2 To 8 Years Skills :- Experience :- Manufacturing:- IPQA | Sterile Validations | AQA Microbiology Division :- Formulation Interview Date:- 29-11-2025 Work Location:- MSN Formulation UNIT-2 Kothur | MSNF -V , China Chilkamarri Inteview Location :- MSN Formulation UNIT-2 Kothur, Survey Nos.1277 & 1319 to 1324, Nandigama (Village),Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out o...

Walk In Drive For Microbiology Department In Formulation Division @ Kothur Department :- Microbiology Qualification :- BSC | MSC - (Microbiology| Biotechnology | Biochemistry ) Experience :- 2 to 8 Years Division :- Formulation Interview Date:-29 -11-2025 Interview Time:- 9.00AM TO 2.00PM Work Location :- MSNF-II, Kothur,MSNF-V R.K.Puram Venue Location:- MSNF-II, Kothur Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Note:- Candidate should bring Update Resume , Certificates, Aadhaar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to ma...

Roles and Responsibilities Conduct IPQA activities, including BMR reviews, stability studies, and batch release. Perform AQA tasks such as sampling, testing, and reporting of results. Ensure compliance with regulatory requirements through validation protocols and reports. Collaborate with cross-functional teams for formulation development and product launches. Maintain accurate records of all quality-related documents and data. Desired Candidate Profile 2-5 years of experience in Quality Assurance (OSD) or related field. B.Sc. / M.Sc. / B. Pharm / M. Pharm Section: IPQA, AQA, Validations Strong understanding of GMP, cGMP and other relevant regulations. Only OSD Formulation experience is cons...

Roles and Responsibilities Conduct analytical data reviews to ensure compliance with regulatory requirements and company standards. Perform OOS investigations, root cause analysis, and CAPA implementation as per SOPs. Collaborate with cross-functional teams to resolve quality issues and improve processes. Develop and maintain documentation for analytical methods, protocols, and reports according to cGMP guidelines. Ensure timely completion of tasks assigned by supervisors while maintaining high-quality output.

Dear All, We are looking for Analytical QA Executive with 2-5 years of experience in pharmaceutical formulations. Key Responsibilities: 1. Review of analytical raw data and reports pertaining to registration stability and compilation of stability data. 2. Review of analytical raw data for Raw materials, in process, finished product and pilot bio/exhibit batch. 3. Review of method transfer protocols, raw data, LNBs and reports. 4. Review of method verification & method equivalency, dissolution profiling protocols, raw data, LNBs and reports. 5. Qualification of spread sheets. 6. Review of Specifications, STPs and GTPs of raw material, packaging material, in-process and finished product (relea...

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...

Role & responsibilities Quality Control-(Chemist to Executive): 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 -(Officer to Manager): Ensure cGMP and regulatory compliance across all QA o...

Walk In Drive For Quality Assurance Sterile In Formulation Division - Kothur Department:- Quality Assurance Sterile Formulations Qualification :- B Sc | B Pharmacy | M Pharmacy| M.sc Experience :- 2 To 8 Years Skills :- Experience:- Manufacturing:- IPQA | Sterile Validations | AQA | Microbiology Division :- Formulation Interview Date:- 15-11-2025 Work Location:- MSN Formulation UNIT-2 Kothur | MSNF -V , China Chilkamarri Inteview Location :- MSN Formulation UNIT-2 Kothur Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out ...

Preparation, review and approval of stability summary report. Preparation, review of freeze thaw study protocol and report Preparation, review of temperature cycle study protocol and report. Required Candidate profile To review AMV, STP, specification, worksheet of finished and raw material packaging material & To Review and implement Validation protocol for process, equipment, cleaning and Analytical Validation.

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top manag...

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.