Quality Assurance Specialist: QMS & Process Improvement

Jazz Pharmaceuticals, Inc.; Maidstone; On-site; GBP 65,000 - 85,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Retirement savings plan

Flexible paid vacation

Job summary

Jazz Pharmaceuticals, Inc. in Maidstone, United Kingdom seeks a Quality Compliance Manager to support the implementation of the Quality Systems at the KSP facility and contractor sites.

You will manage CAPA, deviations, change control, supplier and customer complaints, QRM and root cause analysis, and training within the QMS. You will liaise with global process owners to ensure consistency in the QMS across sites and functions, collate QMS metrics and participate in QMR meetings, ensuring

Qualifications

• Minimum 3 years relevant work experience in the Pharmaceutical, Biotechnology or a related industry
• Experience in GMP, GACP and GDP within a quality environment
• Ability to prepare, review and update QMS documentation
• Collaboration with global process owners to ensure QMS consistency
• Strong communication and training skills for QA teams

Responsibilities

• Prepares, reviews, updates and completes QMS processes
• Ensures training records are kept up to date
• Ensure all complaints are documented, investigated and closed out within guidelines
• Strives to ensure quality events are closed within timeframes and manages events across KSP
• Authors and edits SOPs associated with the QMS at KSP
• Create training packages for QMS processes at KSP

Skills

Office IT skills

Written and verbal communication

Job description

Jazz Pharmaceuticals, Inc. in Maidstone, United Kingdom seeks a Quality Compliance Manager to support the implementation of the Quality Systems at the KSP facility and contractor sites.

You will manage CAPA, deviations, change control, supplier and customer complaints, QRM and root cause analysis, and training within the QMS. You will liaise with global process owners to ensure consistency in the QMS across sites and functions, collate QMS metrics and participate in QMR meetings, ensuring