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Join our dynamic team as a Data Assurance & Quality Classifier in the pharmaceutical industry. This role involves interpreting and validating regulatory submissions, ensuring high operational standards. It offers hybrid working arrangements and exceptional benefits.
Job Responsibility:
Collaborate with Delivery Leads to meet service level and legislative targets
Prepare high-quality case folders for professional assessment and timely allocation
Validate and process regulatory submissions, referencing supporting documentation for medical product licensing applications
Liaise with applicants and assessors to resolve validation issues or inadequate documentation
Develop a robust knowledge of National and European regulatory procedures to effectively validate product licence applications
Requirements:
Proven data entry skills and experience in regulatory submissions validation
Strong understanding of medicines legislation and regulatory procedures
Exceptional communication skills for effective interaction with colleagues and external applicants
A keen eye for detail and a proactive approach to operational performance management
What we offer:
Weekly Pay: Get paid every Friday
Easy Timesheet Access: Mobile support for hassle-free timesheet submissions
Up to 29 Days Annual Leave: Enjoy your time off
Discount Schemes: Access perks at major retailers and over 150 high street stores
Eye-Care Vouchers: Discounts on glasses for VDU use
Well-Being Platforms: Access resources to support your mental and physical health
Free LinkedIn Learning: Enhance your skills with thousands of online courses
Temp of the Month Awards: Recognition for outstanding work
Dedicated Consultant Support: personalised assistance throughout your job journey
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