Lucy Stendall is recruiting for a Regional Labelling Associate to join one of the largest pharmaceutical companies in the world, driven by innovation at their site based in Basingstoke on a contract basis for 12 months initially.
Our client is an innovative company where you will have the opportunity to support the work of thousands of others around the globe dedicated to improving the lives of others. They discover and brings life-changing medicines to those who need them, improving the understanding and management of disease and giving back to communities through philanthropy and volunteerism. Their values are integrity, excellence and respect for people.
This role is located in Basingstoke at our clients Headquarters, which has a train station on the main line from London to Southampton as well as a line to Reading. Alternatively the town is conveniently situated on the M3 motorway and is just one hour from London and Southampton. The A33 also links the town with Reading and the M4.
-Be responsible for the control and coordination of regulatory label creation and change activities and for providing support to Affiliate Labelling Responsible Persons (ALRPs) for the development of high quality, timely, cost-effective artwork.
-Support the artwork development process for new products, changes in existing products and marketing authorization transfers and liaise with ALRPs and PPM (Printed Package Material) to coordinate artwork development and change process timelines.
-Provide ongoing training and coaching to ALRPs to support the regulatory label creation and change process, to keep them informed of current information, and to share learnings from recent experiences.
-Initiating the artwork development or change process by ensuring the information needed to begin the process is accurate and the request is submitted to PPM in a timely manner as well as managing communications between ALRPs and Global Regulatory, PPM, Manufacturing, Quality and the Art Studios, ensuring all parties are aware of the status of changes, new requests, priorities and any issues and ensuring that the information required for the change is available and current.
-Actively participating in labeling Excellence team discussions to align and share information across the team.
-Generating and reviewing metrics to identify and address issues and promote on-going improvements.
-Educated to degree level or above in life sciences or a related field with previous experience of working with Regulatory Affairs Labelling.
-Excellent communication, project management, organisational and problem solving skills.
-Demonstrated ability to communicate and negotiate solutions to complex technical challenges with cross-functional internal and external business partners.
Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference KA43080 in all correspondence.
You must be eligible to work in the UK. Learn more
- Agency: CK Group (Science, Clinical, Engineers and IT Recruitment)
- Contact: Lucy Stendall
- Phone: 01246 457733
- Reference: KA43080
- Posted: 10th August 2018
- Expires: 7th September 2018