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8.0 - 13.0 years
3 - 6 Lacs
Chandigarh, Baddi, Una
Work from Office
QA Senior Executive / Quality Assurance Manager CTC UPTO 6 LPA, Contact: 09990842892 Email: info@wellgen.in We are a 30-year-old Medicine Manufacturer Company is located in Baddi Experience : Minimum 7 years of Pharmaceutical Experience Qualification : B.Pharm 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 mai...
Posted 5 months ago
4.0 - 9.0 years
3 - 8 Lacs
Ahmedabad
Work from Office
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
Posted 5 months ago
1.0 - 5.0 years
3 - 7 Lacs
Hyderabad
Work from Office
We seek a meticulous Quality Engineer to champion quality excellence in our expanding renewable energy projects at Solon India Pvt Ltd. As a Quality Engineer, you will play a crucial role in ensuring the planning, procurement, installation, and commissioning phases of our solar power projects meet the highest quality benchmarks. Your responsibilities will include developing and implementing QA/QC plans, conducting rigorous inspections of incoming materials and site installations, and maintaining comprehensive Quality Documentation. You will collaborate closely with cross-functional teams, including procurement, design, and site execution, to enforce compliance with ISO 9001, IEC, IS, and oth...
Posted 5 months ago
2.0 - 7.0 years
2 - 7 Lacs
Visakhapatnam, Hyderabad
Work from Office
Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Quality Assurance Executive & Sr.Executive injectables&OSD for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. 1.IPQA 2.QMS 3.AQA 4.Validation 5.Equipment Qualification 6.CSV 7.Market Complaints. The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to prasanthi@mydashboards.in or feel free to call on 6305391924 Thanks and Regards Prasanthi - Dashboards Team HR
Posted 5 months ago
3.0 - 8.0 years
2 - 7 Lacs
Ahmedabad
Work from Office
Role & responsibilities Department: Quality Assurance Skill set: 1)QA- stability & Retain sample 2) Doc cell 3) QA Regulatory Designation: Officer/ Sr. Officer/ Executive/ Sr. Executive Education: M.Sc / B.Pahrma / M.Pharma Experience: 2 to 10 Department: OSD Packing Skill set: Operate and monitor primary packing machines such as blister packing, strip packing, and bottle packing machines.,Perform in-process checks like weight variation, visual inspection, and seal integrity. Designation: Officer/Executive Education: B.Pahrm/Diploma/ITI Experience: 2 to 10 years Department: CQA Skill set: 1) Doc Team (Candidates from QC background with LIMS handling experience can apply) 2) CQA compliance + ...
Posted 5 months ago
6 - 10 years
5 - 10 Lacs
Vadodara
Work from Office
To prepare and review vendor qualification SOP, Contract Service Provider and Contract Manufacturing in line with current regulatory requirements To review and compilation of vendor qualification documents & to carry out Vendor Qualification/ Requalification, Service provider Qualification/ Requalification activity and Contract Manufacturer Qualification/Requalification activity. To perform risk assessment, performance evaluation of vendors, handling of change notifications. Handling of Vendor complaint management system. To maintain QM Info record in SAP & to block the materials in SAP. Updating & maintaining the Vendor list, Technical Agreements for Raw material, Packing material, Service ...
Posted 5 months ago
4.0 - 9.0 years
7 - 10 Lacs
ankleshwar
Work from Office
Role & responsibilities Ensure compliance of vendor Qualification Programme. To Perform vendor audit of KSM and Intermediate vendors and External laboratories & preparation of audit report. To make sure that satisfactory CAPA received from vendors timely Review of all vendor qualification documents as per requirements for KSM, Intermediate, Common Raw Materials and Packing Materials. To perform required transaction in SAP system as per responsibilities. To perform vendor qualification of new/ Alternate vendor and Q-info related activities in SAP system for KSM, Intermediate, Common Raw Materials and Packing Materials. Initiation of change control and deviation related to vendor qualification...
Posted Date not available
11.0 - 20.0 years
9 - 15 Lacs
pune
Work from Office
Role & responsibilities Quality Management system Review / approve Master documents like Batch documents, Specifications, Standard Test Procedures, artworks, Methods and other Good Manufacturing Practices (GMP) / quality related documents. Review/approve Site Master File (SMF), Validation Master Plan (VMP), Quality Manual and other organizational Quality Management System (QMS) related documents. Authorize to approve GMP/QMS documents, policies & protocols. Ensure that documents are prepared & implemented that meet GMP requirements. Approve/Reject Change Control, Deviation, CAPA and follow up for the closer of the same. Review / approve investigations, CAPA proposal & risk assessment. Attend...
Posted Date not available
10.0 - 18.0 years
12 - 17 Lacs
pune
Work from Office
Quality Management System: Oversight/Handling of Handling of Change Control, Incident / Deviation and CAPA. Following and tracking of Change Control, Incident /Deviation and CAPA. Involved in the investigation activity whenever required. Ensure that products are manufactured in compliance to Regulatory requirements and as per Good Manufacturing Practices. Ensure that production and manufacturing activities are undertaken in compliance to SOPs, systems, procedure and GMP/GLP requirements. Maintain GMP compliance in various departments to manage the production in line with the current GMP requirement. Handling of Change Control, Deviation, risk assessment and CAPA as per company procedure Veri...
Posted Date not available
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