Determine the regulatory strategy and requirements for launching new medical device and toiletry products into new markets. Communicate to the Business as to updates on regulatory legislative changes and their implications
Project manage the necessary technical activities associated with the implementation of new products in existing and new markets, and support local Product Managers as required, particularly in development of Technical files and data for each product,
Lead and manage the development of artwork for new and updated products
Develop, implement and maintain the quality management system, and support the management of product recalls, investigations, and follow up of quality issues and complaints.
Co-ordinate the quality and corporate and social accountability audit requirements in support of product launches and ongoing compliance by our contract service providers. Take part in strategic supplier review.
Build and maintain relationships with multi functional teams internally and externally (Notified Bodies) to support the effective delivery of the role.
Support a culture of best practice to drive 100% compliance to processes to drive consistency and efficiency.
Typically this sought after person would be degree qualified person in a science or related subject together with at least 10 years commercial experience working within the medical devices sector, an excellent knowledge of Medical Devices legislation and Quality System Management.
This is a global role, with significant responsibilities and demanding strong leadership qualities but in itself a huge career opportunity. Additional languages would be a bonus
For more information on this vacancy, or any other medical device opportunities, please contact the Senior Consultant Andrew Boroky on 0044 (0) 207 940 2116, or email him at firstname.lastname@example.org
Posted: 16/08/2012 | NPJ Ref: 85145