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Preproduction Coordinator

2 months ago

Bathgate, West Lothian, United Kingdom Catalent Full time
About the Role

Catalent is seeking a highly detail-oriented Preproduction Coordinator to join our team in Scotland, UK. As a key member of our Operations team, you will play a crucial role in ensuring the integrity of clinical trial supplies packaged at our site.

Key Responsibilities
  • Generate clinical trial packaging documentation to meet Catalent, client, study, and regulatory requirements.
  • Complete documentation in accordance with relevant SOPs and to comply with Good Manufacturing Practice (GMP).
  • Maintain high-quality standards, ensuring all deviations are documented as required.
  • Report any issues that may impact the quality or timelines specified for the packaging of supplies to your Line Manager.
  • Competently perform tasks as detailed by the Preproduction skills matrix.
  • Participate in the implementation of new systems or upgrades to systems pertaining to the Preproduction department.
  • Maintain a personal training record and attend training sessions as required.
  • Participate in process improvement initiatives to support the Preproduction department, site, or wider Catalent organization, as appropriate.
  • Stay up-to-date with industry best practices.
Requirements
  • Attention to detail
  • Confident user of Microsoft packages
  • Pharma/clinical trials experience or education highly advantageous
  • Experience in GMP or GDP highly advantageous
  • Proactive
About Catalent

Catalent is a global leader in the development and delivery of pharmaceutical, biologic, and consumer healthcare products. We produce over 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.