Packaging Co-ordinator

**Packaging Co-ordinator**

**Sandwich**

**12 months Temporary contract**

**Hybrid**

**Full-time**

**£14.50 - £17.15 DOE**

Tate recruitment is working in partnership with a well know pharmaceutical company based in Sandwich. We are looking for a Packaging Co-ordinator who wants an opportunity to work for an established organisation.

**ROLE RESPONSIBILITIES**
- Providing Clinical Packaging expertise to our stakeholders, while maintaining an organisational culture that values flexibility, continuous improvement and an agility to meet business needs
- Work with the Supply Chain Leads (SCL), Operational Strategy Lead (OSL), and Clinical Research Pharmacist (CRP) to review and interpret the clinical protocol to develop practical and efficient packaging designs for Clinical Supplies
- Coordinate and communicate multiple study packaging and/or labelling requirements across a network of global packaging vendors and internal packaging facilities
- Be compliant with cGMPs when ensuring the delivery of clinical supplies
- Utilise Project Management skills to plan, schedule and assess risks to complete the packaging operation
- Prepare/Approve packaging documentation and generate internal study paperwork to support packaging operations
- Review internal/contractor packaging and labelling documents making recommendations where appropriate to ensure compliance with Clinical Supply Operations procedures, study requirements and Good Manufacturing Practice (cGMPs)
- Work with Inventory Management, Quality Assurance and Global Analytics to co-ordinate and drive the progress of the packaging operation to ensure timelines are met
- Facilitate the use of Clinical Supply Distribution System (CSDS) for importing packaged inventory for distribution purposes
- To support assigned Global Clinical Supply or Clinical Supply Operations continuous improvement initiatives

**BASIC QUALIFICATIONS**
- B.S. degree within a scientific discipline or 5 years equivalent experience
- PMP certification or demonstrated project management experience
- Experience working in a GMP regulated work environment

**PREFERRED QUALIFICATIONS**
- Knowledge of clinical trial study designs is preferred

Tate is acting as an Employment Business in relation to this vacancy.