35 Aqa 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, d...

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...

Walk In Drive For Microbiology Department In Formulation Division @ Kothur Department :- Microbiology Qualification :- BSC | MSC - (Microbiology| Biotechnology | Biochemistry ) Experience :- 2 to 6 Years Division :- Formulation Interview Date:- 13-09-2025 Interview Time:- 9.00AM TO 2.00PM Work Location :- MSNF-II, Kothur 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 make health care af...

Walk In Drive Quality Assurance Department In Formulation Division @ Kothur Department :- Quality Assurance OSD Qualification :- B Sc | B Pharmacy | M Pharmacy | MSC Experience :- 2 to 8 Years Skills:- AQA | IPQA|CQA| IPQA MFG|IPQA Packing Division :- Formulation Interview Date:- 13-09-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- MSN Laboratories Pvt Ltd,. Formulation Unit-02,Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those who have experience in QA OSD (IPQA,AQA,Packing,Documentation,Valid...

Responsible for detailed review of Finished Products, In-Process, Raw material and Stability study analytical reports along with audit trail review of each analytical data. - Responsible for review of stability study protocols of annual batch or validation batch and ensure for charging of stability study sample. -Responsible for review of stability summary sheets of stability analytical data - Responsible for review routine monitoring data of stability chambers - Responsible for review of laboratory incidents investigations and its closure. - To comprehensively review the audit trail logs of laboratory software - To ensure the overall compliance level of laboratory as per guidelines and stan...

We are seeking a meticulous AQA - Data Reviewer to conduct quality reviews of key pharmaceutical documents and ensure compliance with regulatory standards, including 21 CFR. The ideal candidate will collaborate with cross-functional teams to maintain document integrity and support continuous quality improvement. Key Responsibilities: Conduct thorough quality reviews of documents such as CAPAs (Corrective and Preventive Actions), change controls, and ensure compliance with 21 CFR regulations. Ensure adherence to company policies and standard operating procedures through detailed document reviews. Develop and maintain a comprehensive understanding of pharmaceutical regulatory requirements. Pro...

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...

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 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...

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...

Role & responsibilities Ensure compliance with cGMP, regulatory, and internal quality standards. Manage QMS activities deviations, change controls, CAPA, OOS/OOT, document control, etc. Handle Analytical Quality Assurance (AQA) activities data review, audit readiness, and compliance monitoring. Oversee In-process Quality Assurance (IPQA) – batch manufacturing records review, shop floor monitoring, line clearance, process compliance. Conduct internal audits, support external audits (regulatory and customer), and ensure timely closure of audit observations. Drive new initiatives in digitalization, automation, and process improvement in QA systems. Training and mentoring of team members to stre...

5-7 Years experience having AQA review knowledge Audit trail review, QC incident review and stability managements Review and approve analytical data, reports, and method validation documents. Ensure compliance with GMP , GLP , and regulatory requirements . Perform quality checks on raw data, chromatograms, and calculations. Participate in laboratory investigations and audits. Support continuous improvement and data integrity initiatives.

Excellent job opportunity for QA - AQA Specialist in Unison Pharmaceuticals Pvt Ltd, Moraiya, Ahmedabad About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. You are invited to join one of India's fastest growing pharma companies in India!! Experie...

Role & responsibilities Analytical QA Review the analytical documents which are generated after analysis of Drug Products. Preparation and Review of all Departmental SOP's for cGMP Compliance. Compilation and Review of the Batch Records, Certificate of Analysis, Analytical Protocol, etc which are required for release of Batches. Review and Approve SOPs, Change Controls, Deviations, Annual Product Quality Reviews, Incident Reports, Out of Calibrations, Out of Specifications, Out of Trends, Approve the Investigation Reports. Market Compliant, & manage Stability Samples etc. Review of Regulatory Requirements and its Compliance. Periodic review of all Quality functions and Procedure for appropri...

Roles Open: QA (QMS, Validations and AQA): Qualifications, Process/Cleaning Validation, QMS (Change Controls, Deviations, CAPA, Complaints, and OOS) RA (Regulatory Affairs): CTD Preparation/Review, Regulatory Queries, Tech Transfer Documents. Required Candidate profile QA Executive / Sr. Executive (QMS & Validations) AQA Executive / Sr. Executive (Analytical QA) RA Executive / Sr. Executive – Regulatory Affairs

Responsible for overall Quality control laboratory Implementation of cGMP and good laboratory practices. Handling of laboratory incident, Out of calibration and deviation investigation. Conducted investigations on product/material test results failures and out of trends Review & approval of standard test procedure, specification Handling of laboratory incident, Out of calibration and deviation investigation. Making sure that all deviation, OOS,OOT, incident are investigated and closed before the release of the batch/material

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...

Walk-in Drive for API-Quality roles!!! Walk-in Dates: Friday July 25 & Saturday July 26, 2025 Time: 1000 hrs. to 1600 hrs. Address: Emcure Pharmaceuticals Ltd. D-24, M.I.D.C., Kurkumbh, Tal- Daund, Dist.- Pune, PIN- 413 802, Maharashtra, India. API-Quality Control M.Sc. (Analytical / Organic Chemistry) with 2-5 years of experience in Expertise in handling RM, intermediates & Finished products in API manufacturing. Handling HPLC, GC, LCMS, GCMS, ICPMS, Particle Size analyzer, and hands-on experience on Empower 3 & Chromeleon software preferred. API Quality Assurance- QMS & IPQA M.Sc. (Organic Chemistry, BE/ B. Tech- Chemical Engineering) with 2-8 years of experience in Must have experience in...

Role & responsibilities Audit Trail Review Batch Release Method Validation & Transfer Review Calibration Records Review Analytical Raw Data Issuance OOS, Lab Deviation CAPA QC Review Experience in handling audits Preferred candidate profile Should have participated in Audits and exposure towards it Should be qualified in Chemistry knowledge in process and production Smart enough to understand the regulatory requirements Knowledge in regulatory and GMP. Perks and benefits As per Company norms

Strong 1-4 years of knowledge and Experience in Analytical QA

Role & responsibilities For Production : Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions (Handling of Homogenizer, Netzsch Mill/Bead Mill and Single use Systems) filtration, Lyophilizes. Having Injectable Experience of Shop floor supervising activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions (Handling of Homogenizer, Netzsch Mill/Bead Mill and Single use Systems) filtration, Lyophilizes. Operations and Training and QMS. For Quality Assurance : Having Injectable Experience of QMS, Audit & Compliance, IPQA, AQA (...

Roles and Responsibilities Conduct quality audits, BMR reviews, CAPAs, deviation investigations, change controls, equipment qualifications, process validations, and vendor qualifications. Ensure compliance with USFDA regulations through IPQA activities Engineering Documentation ,Qualifications &Validations. Warehouse Documentation ,Qualifications &Validations. Cleaning Validation Perform analytical QA tasks such as OOS management and sterility testing. Participate in MHRA / USFDA inspections by providing necessary documentation and supporting audit findings. Collaborate with cross-functional teams to resolve quality issues. Regulatory Audit Exposer LIKE FDA, MHRA, TGA Audit Reponses and Audi...

HIRING FOR FORMULATION UNIT - INJECTABLE/ OSD JOB DESCRIPTION AND EXPERIENCE: WORK LOCATION: Hetero Labs Limited, UNIT V & VI, Polleypally, Jadcherla, Mahabubnagar PRODUCTION(OSD) Experience: (02-07Years) Compression, Granulation, Coating, Capsule filling, Inspection PRODUCTION (INJECTABLE) Experience: (02-07Years) Autoclave, Compounding, filling, QMS, Vial Washing, Lyophilizer, Visual Inspection PACKING (INJECTABLE/OSD) Experience: (01-05Years) Blister Packing, Bottle Packing. QC & QC- Micro Experience: (02-07Years) HPLC, GC, RM,PM, Stability, IP/FP,MLT, Environmental monitoring, QA-INJECTABLE Experience: (02-07Years) IPQA, Validation, Qualification, CSV, AQA (QC & Microbiology) WAREHOUSE E...

Dear All, We are conducting Walk-In Interview on 13th June 2025(Friday) for Quality Assurance and Quality Control( Formulations ) departments. Quality Assurance: AQA - 6-8 Years of experience in Analytical QA IPQA - 2-4 Years of experience in Line Clearance activities for Production, Warehouse and Dispensing of Raw Materials Quality Control: IPFP - 4-5 Years of experience in HPLC, GC, UV, Dissolution and RS. Stability - 4-6 Years of experience in Dissolution, GC, UV and Sample management Raw Materials - 2-3 Years of experience in sampling of Raw and Packing materials Analytical Method Validations - 3-5 Years of experience in Method validations, HPLC and Dissolution instruments Microbiology -...

Roles and Responsibilities (Hiring for AQA Role, IPQA Role, QMS Role - API Background is Must) Ensure compliance with GMP, BMR, BPR, SOPs, and quality systems. To Perform Analytical QA Role IPQA Activities QMS Activities Validation Activities Collaborate with cross-functional teams to ensure timely completion tasks Person Should be from the API Background