3 of 3 Permanent Contingency Planning Jobs in Scotland

below: What You’ll Be Doing: Coordinating and carrying out validation for both custom-developed and commercial off the shelf systems used across regulated environments Supporting lifecycle management from planning onwards, ensuring documentation and compliance remain watertight Conducting risk assessments to determine validation scope and strategy based on Good Practice relevance Creating and maintaining validation documentation such as user …/functional requirements specs/validation planning/protocols/reports/etc. Liaising with internal teams and vendors to deliver compliant system implementations aligned to Good Automated Manufacturing Practice and agreed standards Acting as a key contact for audit and inspection activity concerning data integrity and system validation Taking part in DR testing for critical systems and assisting … with contingency planning Helping evolve internal policies, templates, and working practices to keep pace with regulatory expectations What You’ll Bring: Proven background in a similar role/s in IT/Engineering/Life Sciences/similar domains Familiarity with regulatory frameworks including Good Automated Manufacturing Practice and similar relevant offerings Track record of working with both More ❯

below: What You’ll Be Doing: Coordinating and carrying out validation for both custom-developed and commercial off the shelf systems used across regulated environments Supporting lifecycle management from planning onwards, ensuring documentation and compliance remain watertight Conducting risk assessments to determine validation scope and strategy based on Good Practice relevance Creating and maintaining validation documentation such as user …/functional requirements specs/validation planning/protocols/reports/etc. Liaising with internal teams and vendors to deliver compliant system implementations aligned to Good Automated Manufacturing Practice and agreed standards Acting as a key contact for audit and inspection activity concerning data integrity and system validation Taking part in DR testing for critical systems and assisting … with contingency planning Helping evolve internal policies, templates, and working practices to keep pace with regulatory expectations What You’ll Bring: Proven background in a similar role/s in IT/Engineering/Life Sciences/similar domains Familiarity with regulatory frameworks including Good Automated Manufacturing Practice and similar relevant offerings Track record of working with both More ❯

below: What You’ll Be Doing: Coordinating and carrying out validation for both custom-developed and commercial off the shelf systems used across regulated environments Supporting lifecycle management from planning onwards, ensuring documentation and compliance remain watertight Conducting risk assessments to determine validation scope and strategy based on Good Practice relevance Creating and maintaining validation documentation such as user …/functional requirements specs/validation planning/protocols/reports/etc. Liaising with internal teams and vendors to deliver compliant system implementations aligned to Good Automated Manufacturing Practice and agreed standards Acting as a key contact for audit and inspection activity concerning data integrity and system validation Taking part in DR testing for critical systems and assisting … with contingency planning Helping evolve internal policies, templates, and working practices to keep pace with regulatory expectations What You’ll Bring: Proven background in a similar role/s in IT/Engineering/Life Sciences/similar domains Familiarity with regulatory frameworks including Good Automated Manufacturing Practice and similar relevant offerings Track record of working with both More ❯