The Global Regulatory Affairs Director will be responsible for regulatory strategy in a speciality manufacturing business across multiple sites and locations.

Client Details

The business manufacture a range of speciality chemicals and pharmaceuticals. A fast-growing business with multiple sites across the world they offer a career path and opportunity for leadership candidates to progress and make a real positive impact.

Description

The Global Regulatory Affairs Director will be responsible for leading regulatory strategy and providing a proactive policy for the business. You will interpret regulations and policies across multiple regions and advise the cross-functional teams on regulatory requirements. In addition you will represent the regulatory team on global executive committees and with customers. You will regulate and validate framework on specific products and ensure that training is implemented at all levels of the business. You will improve existing policies and procedures and lead continuous improvement activities across the business.

Profile

The successful candidate will have a PhD or Masters Degree in a scientific or related discipline with a proven track record of Regulatory leadership within a Chemical/Pharmaceutical or FMCG environment. You will have strong leadership capability, having presented to board level and to key customers around all regulatory matters. You will have thorough knowledge fo FDA, ISO and GMP requirements and worked developing a global regulatory management system and framework before. You will be able to work autonomously and with create accountability through training and mentoring.

Job Offer

The opportunity to impact a large-scale business to develop and improve existing frameworks and procedures. Work with a business that is continuing to expand with new products and processes. Work with a leadership team to develop strategy and have ultimate control over decisions.

Competitive Salary & Benefits

This is a retained search assignment and all 3rd party applications will be forwarded to Michael Page for consideration.