88380BR Job Family Regulatory Affairs Job Category Full-Time Job Classification Permanent Division Established Pharmaceuticals Shift Days Relocation Assistance None Job Description MAIN PURPOSE: To provide regulatory advice and support to the UK Abbott affiliate

MAIN RESPONSIBILITIES:

• Gain marketing authorisations for new pharmaceutical products in the UK
• Maintain marketing authorisations as required.
• Liaise with European Regulatory Affairs and Corporate groups on regulatory issues.
• Liaise with external regulatory authorities as required.
• Draft of packaging texts, SmPCs, PILs and Prescribing Information.
• Review of promotional material in accordance with The Prescription Medicines Code of Practice Authority (PMCPA)/ABPI Code
• Liaise and attend meetings with other company functions to provide regulatory advice for new products.
• Maintain awareness of current and new legislation/guidance and ensure that work is in compliance with the statutory requirements.

GENERAL RESPONSIBILITY:
Any other reasonable duties as required by the business.

To comply with the company’s policies and procedures to meet statutory, quality and business requirements within the overall strategy and objectives of Abbott Healthcare Products Limited.

ACCOUNTABILITY
Responsible for presentation and accuracy of all prepared documentation.

A moderate level of supervision is required for the Senior Officer role. The position demands that the person is able to recognise the potential impact of emerging issues and highlight these to their line manager.

Accountable to Regulatory Affairs Manager. Skills/Experience Requirements BACKGROUND

• Extensive experience of working in a regulatory environment
• Good communication skills, both verbal and written
• The ability to thrive in a changing environment and to re-prioritise workload to meet business needs.
• Good project management skills

Abbott Laboratories - 11 months ago