41 Qa Executive Jobs - Page 2

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

Tempcon Express Pvt Ltd 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).