Pre-Production Specialist

Catalent is currently recruiting for a Preproduction Coordinator to join our Bathgate team. With nearly 25 years of experience, our Bathgate location in Scotland, UK is an integral part of Catalent's European clinical supply services network.
We are looking for a candidate with a keen eye for detail and excellent written and verbal skills to join the Operations team. The Preproduction Coordinator will ensure the integrity of clinical trial supplies packaged at our Bathgate Site.
The Role
Generate clinical trial packaging documentation to meet Catalent, Client, Study and Regulatory requirements.
Complete documentation in accordance to relevant SOPs and to comply with GMP.
Maintain high quality standards ensuring all deviations are documented as required.
Report to your Line Manager any issues which may impact on the quality or timelines specified for the packaging of supplies.
Competently perform tasks as detailed by the Preproduction skills matrix.
Participate in the implementation of any new systems or upgrades to systems pertaining to Preproduction department.
Maintain a personal training record and attend training sessions as required.
Participate in any process improvement initiatives to support Preproduction department, Bathgate site or wider Catalent organisation, as appropriate.
Keep up to date with industry best practice., Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Attention to detail
Confident user of Microsoft packages
Pharma/ clinical trials experience or education highly advantageous
Experience in GMP or GDP highly advantageous
Proactive