Job type
TemporaryLocation
North LanarkshireWorking Pattern
Full-timeSpecialism
Research And DevelopmentIndustry
PharmaceuticalsPay
£45-60 per hour (UMB)
Quality | Pharmaceuticals | Diagnostics | 6 months | Hybrid
What you'll need to succeed
Facilitate the migration of the document management system, ensuring a seamless transition and system integration.
Develop a comprehensive concept for implementing retention time policies for existing paper records, aligning with compliance standards and organisational needs.
Initiate and manage document workflows as required, ensuring efficiency and adherence to operational procedures.
Responsibilities
Document authoring and review as required to support changes.
Performs technical reviews and prepares documentation for audits, as applicable.
Communicating significant quality or regulatory issues and risks that may impact product quality or regulatory compliance in a timely manner to Executive Management.
Identifying and escalating issues as they arise and being able to provide adequate solutions.
Works day to day with minimal supervision to correctly complete daily scheduled and unscheduled activities
Initiate, facilitate, participate and implement process improvements to meet business needs.
- Able to link responsibilities with both site and Global Quality and Regulatory.
You are primarily based in Lanarkshire (Scotland), however, travel to other sites in the Stirling area will be required.
