Began as Northenden Engineering Services before evolving through rebrands and international expansion.
Merged with Fircroft in 2020 to become a global powerhouse.
Operates over 80 offices in 45 countries, deploying workers on major projects.
Supports long-term contracts, permanent hires, managed services, global mobility, and payroll.
Backed by a history of nine strategic acquisitions, enhancing reach in sectors like chemicals and digital technology.
Delivers talent into high-profile projects such as offshore wind farms, petrochemical plants, mining developments, and pharmaceutical facilities.
About the client
About the client
Information not given or found
Role
Description
protocol review
vendor management
preventive maintenance
process optimization
change control
equipment revalidation
Ensure all company and site engineering policies and procedures are adhered to.
Provide technical and compliance review and/or authorship of testing protocols, reports and applicable manufacturing SOPs.
Management of Equipment Vendors including execution of on-site maintenance visits, management of continuous improvement projects & spare parts criticality assessments.
Support establishment of new Preventative Maintenance Program for equipment in Drug Product suite.
Lead and participate in cross-functional teams to troubleshoot and resolve technical issues, drive continuous improvement, and process optimization using tools such as DMAIC and FMEA.
Manage changes to equipment/process as per site change control procedures.
Support/lead maintenance of the validated state of the equipment through execution of revalidation protocols as per Site VMP.
Provide technical leadership within a new Vaccine Drug Product Manufacturing facility.
Generate and execute documentation for cGMP activities including risk assessments /reports.
Ensure all equipment installed is safe, effective and in compliance with industry standards.
Requirements
cgmp
six sigma
adaptability
investigation
fat
fmea
Minimum 5 years cGMP industrial / engineering experience,
Experience in data driven approach to root cause analysis and prioritization of continuous improvement initiatives e.g. Six Sigma
Ability to adapt to changing priorities as project demands change.
Experience in leading & resolving complex technical investigations.
Experience in executing on the floor activities such as FAT, SAT, IQ/OQ
Experience in a risk-based approach to manufacturing through use of tools such as FMEA