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Quality Assurance Associate
View: 108
Update day: 13-05-2024
Category: Sales
Industry: Chemical Manufacturing
Position: Associate
Job type: Full-time
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Job content
R00188026Purolite, an Ecolab company, the world leader in resin-based separation, purification and extraction technology, is seeking a Quality Assurance Associate.At Purolite, we manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It’s an exciting business which helps make the world cleaner, safer and healthier.As a Quality Assurance Associate you will verify all operations are compliant with internal procedures and regulatory requirements. The Quality Associate will support the development and implementation of the QA systems during the scale-up and manufacture of products that service global pharmaceutical markets. Ensure the needs of both internal and external customers are met through efficient use of the quality processes and the systems available. Where required there may be the need to support validation, inspections and system development as the site evolvesWhat You’ll Do- Act as first line support and system administrator for the company’s electronic management system Q-Pulse; assists with development, implementation, and maintenance, as needed
- Troubleshoots existing practices and deviations using quality tools to solve day to day problems as they arise.
- Product release
- Generation of batch numbers and certificate of analysis
- Receipt, acceptance, and approval of raw materials
- Maintain NHBA and Warehouse Stocks
- Support dispatch and ensure shipments and documentation is complete for dispatch
- Participation in the change control process to ensure changes to processes, systems, equipment, and facilities are appropriately assessed and implemented
- Participates in both group and cross-functional process improvement and development initiatives
- Performing audits to monitor compliance of internal operations and inter procedures and regulatory requirements via internal audits.
- Involvement in preparation of customer audits
- Support with Purolite’s vendor management program
- A scientific degree, or equivalent
- Experience in a global regulated environment with a sound understanding of quality system requirements. (cGMP and ISO9001 advantageous)
- Software and technical skills, all Microsoft Office applications. (Q-Pulse or other electronic QMS software an advantage)
- Internal Auditing experience to ISO9001 requirements (cGMP advantageous)
- Experience of Batch Record review advantageous
- The opportunity to take on some of the world’s most meaningful challenges, providing sustainable solutions for our environment, businesses and healthcare
- The ability to make an impact and shape your career with a company that is passionate about growth
- The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best
- Comprehensive benefits package which includes pension, holiday allowance and life assurance at 4x your salary
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Deadline: 27-06-2024
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