26 Qa Executive Jobs

Job Title: Sr. Officer / Executive QA Business Unit: Global Quality & Compliance Job Grade G12B /G12C Location : Ahmednagar / Ahilyanagar At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Key responsibilities: Responsible for ...

Developing and executing manual and automated tests Identifying and reporting software defects Collaborating with development teams to ensure that software meets quality standards Designing and maintaining test cases and test plans Participating in code reviews to identify potential quality issues Strong understanding of software development and testing methodologies Knowledge of software testing tools and techniques Experience with manual and automated testing Excellent problem-solving and troubleshooting skills Strong communication and collaboration skills

Blancher area: ensure that equipment is set to the standard required for the specific product process. Monitor water levels, quality, and usage. o Ensure temperature, retention times, alarms are all set within the RS view system. Monitor / record yield loss, colour, texture and any breakage. SAAP / Dextrose System: ensure that equipment is set to the standard required for the specific product process. Monitor Dextrose / SAPP percentage, water quality and ingredient usage. Ensure temperature and alarms are all set within the RS view system. Monitor / record colour and any breakage. Dryer Area: ensure that equipment is set to the standard required for the specific product process. Ensure tempe...

1. Position: Executive QA Location: Factory, MIDC Tarapur Location: Factory, MIDC Tarapur Details: Will report to Manager QA Manage daily acitivites independently. Handle QC related activities of the QA department Coordinate between departments Excellent troubleshooting abilities Supporting in the Quality Management System Supporting in Incidents, Deviations, OOS. Taking appropriate CAPA Requirements: BSc with min 5 years?experience or MSc with 3 years?experience Along with minimum 1-year experience in Quality Assurance Department Understanding of HPLC, GC, UV, IR and other Analytical techniques

AAKASH INFOTECH is looking for QA Executive to join our dynamic team and embark on a rewarding career journey. You will also be responsible for identifying and resolving quality - related issues and ensuring that the company's products and services meet the requirements of customers. Conduct regular quality audits to identify and resolve quality - related issues. Develop and maintain quality metrics to track performance and identify areas for improvement. Manage the documentation process for quality assurance procedures, including the creation and maintenance of standard operating procedures (SOPs).

Position Title: Operator - Process Position Type: Regular - Full-Time Position Location: Mehsana Grade: Grade 01 Requisition ID: 37019 Global Job Descriptions Job Details: Function/Department : Production Global Job Grade Job Title* : Process Operator Region** : APEMA Global Grading System Job Code: Global Job Grade : Evaluation Date : March 14, 2012 Global Pay Band : 3 Global Benchmark Job : Yes * This is a generic job title to be used for Job Administration. Job titles used by individuals may vary by country but the position should be aligned to the generic job title for Job Administration purposes. ** e.g. Global/APMEA/NA/CE/etc. Instructions for Position Summary: Brief description of the...

Position Title: Operator- Process (Fryer, Freezer) Position Type: Regular - Full-Time Position Location: Mehsana Grade: Grade 01 Requisition ID: 37016 Global Job Descriptions Job Details: Function/Department : Production Global Job Grade Job Title* : Process Operator Region** : APEMA Global Grading System Job Code: Global Job Grade : Evaluation Date : March 14, 2012 Global Pay Band : 3 Global Benchmark Job : Yes * This is a generic job title to be used for Job Administration. Job titles used by individuals may vary by country but the position should be aligned to the generic job title for Job Administration purposes. ** e.g. Global/APMEA/NA/CE/etc. Instructions for Position Summary: Brief de...

Position Title: Operator- Process Mixture & Preparation Position Type: Regular - Full-Time Position Location: Mehsana Grade: Grade 01 Requisition ID: 37017 Global Job Descriptions Job Details: Function/Department : Production Global Job Grade Job Title* : Process Operator Region** : APEMA Global Grading System Job Code: Global Job Grade : Evaluation Date : March 14, 2012 Global Pay Band : 3 Global Benchmark Job : Yes * This is a generic job title to be used for Job Administration. Job titles used by individuals may vary by country but the position should be aligned to the generic job title for Job Administration purposes. ** e.g. Global/APMEA/NA/CE/etc. Instructions for Position Summary: Bri...

Quality Assurance Executive required for reputed organisation in Navi Mumbai location Dear Professionals,, I am Sindhura C , from the Pharma Vertical of Masadir HR Services , an International Recruitment Firm. We have been retained by professionally managed organisation to recruit Quality Assurance Executive for them. The job location is in Navi Mumbai. Qualification: Graduate or Postgraduate Degree in Biological or Life Sciences with at least 3-4 years working in QA/compliance domain Experience: Min 2yrs If you are interested in exploring the above opportunity, kindly share your updated resume with me please. In case, if you are not interested, kindly feel free to refer your friends who may...

QA Executive Qualification - B.Sc Chemistry/B.Pharm with 2 years of previous experience in medical devices/pharma. Tasks: Preparation, review & monitoring of Process Validation, machine validation, MOA, Specification, BMR, etc.Issuance, review & retention of all documents generated in organization

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Knowledge of maintaining agricultural produce To maintain standards and specifications of all raw materials and finished products To assist in all areas related to product quality including troubleshooting, visiting, production, facilities, designing, training, quality control panel To provide information that is accurate, reliable and adequate for the intended purpose Keep the management team apprised of the quality issues Responsible for inspecting and documenting all incoming fruit, vegetables, packaging materials, and ensure all product quality standards are adhered to. Perform routine quality and condition inspections on existing inventory to assist in first-in, first-out (FIFO) or wors...

Position Title: Operator- Process Mixture & Preparation Position Type: Regular - Full-Time Position Location: Mehsana Requisition ID: 36783 Global Job Descriptions Job Details: Function/Department : Production Global Job Grade Job Title: Process Operator Region*: APEMA Global Grading System Job Code: Global Job Grade : Evaluation Date : March 14, 2012 Global Pay Band : 3 Global Benchmark Job : Yes This is a generic job title to be used for Job Administration. Job titles used by individuals may vary by country but the position should be aligned to the generic job title for Job Administration purposes. *e.g. Global/APMEA/NA/CE/etc. Instructions for Position Summary: Brief description of the pr...

The QA Executive is responsible for ensuring compliance with GMP, ISO, and regulatory guidelines by conducting audits, inspections, and documentation reviews The role involves overseeing batch record reviews, deviations, CAPA, and change control processes, ensuring adherence to quality standards for raw materials, in-process, and finished products The candidate will also implement quality improvements, handle customer complaints, and support regulatory audits to maintain product integrity and compliance : B Sc / M Sc

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowle...

Handling of Quality management system like Market complaints, Change Control, Deviations, OOS, OOT, Incidents, CAPA, Self-Inspection, Vendor Qualification. Review and Approval BMR/BPRs, Prepare of Standard Operation Procedure, Process Validation, Hold Time Study Protocol and Reports, Annual Product Quality Review & trending, Cleaning validation. Qualification/ requalification of Equipments. Release of Finished Product, Continuous Process Verification, Trainings etc.

04 to 05 Years Experience of QA Documentation . Should be able to conduct IPQA independently. Responsible for Line clearance In-process of all activities. Responsible for review, compilation and closing of Batch manufacturing records and Batch Packing records. Responsible to follow, Good Documentation Practices, Good Manufacturing Practices to ensure the quality standards of company. Verification & monitoring of shop floor activities from dispensing to dispatch. Responsible for manufacturing compliance. Responsible for preparation of relevant SOPs. Monitoring & verification of log books at manufacturing blocks for compliance Desired Candidate Profile The candidate should have adequate knowle...

•Education: M.Sc. Chemistry/ Environmental Science •Experience: 3-8years •Skills :Titration Methods, ,Calibration of pH meter, Operation of UV Visible Spectrophotometer, & Karl Fischer ,ISO &5S, SAP Contact NO :6359660041

Responsibilities: Inspection & Testing: Perform regular quality inspections and tests on incoming raw materials, in-process production stages, and finished products as per defined quality control plans, specifications, and sampling procedures. Utilize various measuring instruments (e.g., calipers, micrometers, gauges) and testing equipment to ensure accurate data collection. Conduct visual inspections to identify defects, deviations, or non-conformities. Process Monitoring & Compliance: Monitor production processes and operational activities to ensure strict adherence to established Standard Operating Procedures (SOPs), work instructions, and quality management system (QMS) requirements (e.g...

What We re Looking For: Qualification: M.Sc. Chemistry / B.E. Chemical / B.Pharmacy Experience: 4-6 years in the pharmaceutical industry Strong knowledge in: QMS, Validation (Process, Equipment, Cleaning), and Qualification (IQ/OQ/PQ) Good documentation skills and regulatory understanding: GMP, FDA, ISO