Job Reference: 1701-83
Job Duration:
Start date: a.s.a.p
Description:
My client, an established Biopharma based in Oxfordshire is currently searching for an experienced Senior Manager Regulatory AffairsLabeling to join their team based in Oxfordshire. Within this role you will be responsible for regulatory support (both technical and operational) in the area of product labelling. You will report to the Head of Global Labeling and you will be responsiblefor key functions including creating, updating and maintaining labeling documents throughout the product lifecycle, with primary focus on Company Core Data Sheets and products marketed globally.
Responsibilities:
-The candidate will help maintain controlled records for historical labeling changes, and communicate labeling changes to stakeholders at the time of implementation.
-Help to implement process improvement changes to increase the efficiency and effectiveness of the label review process.
-This position will interact cross-functionally with members of commercial, legal, safety, medical, and others.
-Maintain expertise regarding key labeling requirements worldwide and stay current with labeling guidelines and regulations as they pertain tothe development/maintenance of labeling and advise key stakeholders on the application of these labeling principles.
-Maintaincontrolled records for historical, current, and ending labeling changes, and communicate labeling changes to stakeholders at thetime of implementation.
-Manage quality control over entire labeling process and management of revisions, including assigning/tracking projects, workflow execution, and issue resolution
-Provide project management to the Labeling Team throughout the entire process, from the decision to update a CCDS/USPI/SPC through notification to stakeholders, to ensure that these documents are produced in a timely manner according to internal SOPs and external regulatory requirements
-Responsible for proofreading anddepartmental QC work
-Lead the development of CCDS, package inserts and equivalents and their associated Patient Labeling Documents
-When developing new labels, research the content of other labels in the same therapeutic class, including competitor labeling, to help guide the team in developing labeling text, including contingency strategy development for negotiation with regulatory authorities.
Minimum Requirements:
-S/B.A. (or equivalent in industry related experience)
-Proven experience in regulatory affairs with particular focus on labelling
-Experience associated with global product labeling regulations strongly desired
-Strong judgment and decision making skills
-Excellent written and verbal communication skills
-Ability to review regulatory labeling documents for accuracy and adherence to regulatory requirements, noting deficiencies and inconsistencies
-Must be able to work successfully within a team/partnership environment and as an individual contributor, with a high level of professionalism
-Ability to interact effectively with all levels/roles of project team members
For further details about this role, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@keypeople.co.uk
Industry: Science and Research
Salary: £55000 - £65000 per annum + bonus and excellent benefits
Salary Benefits: bonus and excellent benefits
Vacancy Type: Permanent
Job Skills: regulatory affairs, labelling, PILs, smpcs, smpc, label, manager, senior manager, senior regulatory affairs manager
Contact Name: Tim Barratt
Website: -
Direct Application URL: -