implementing IT PQS systems (particularly Veeva Vault) Documentation management expertise Essential Skills Excellent documentation writing capabilities Strong communication and collaboration skills Deep understanding of GMP compliance requirements Project management expertise Ability to manage ambiguity and drive results Detail-oriented with strong organizational skills Collaborative team player with stakeholder management abilities More ❯
of PQS IT systems like Veeva Vault. Experience with documentation management Top 3 must have skills Documentation writing skills Communication/collaboration Understanding of GMP compliance Description: Enrolment and site maintenance of the global standards process. Support with the documentation management processes. Support with implementation of the global systems incl. More ❯
projects in accordance with the company project roadmap throughout the project lifecycle ensuring governance to current engineering standards and compliance with CDM regulations. Strict GMP compliance to be adhered throughout the lifecycle of the project. Coordination with the Principal Contractor and all other project team members to ensure completion to … budget and provide accurate monthly reports Attendance at daily update meetings Ensure compliance with all HSE & CDM requirements Ensuring compliance of project delivery with GMP requirements and company UKSL SOP’s Develop and updated project schedule defined appropriately according to project stage-gate Identify, record and monitor project risks, seeking … level Project Engineer/Project Manager with experience in managing cross functional teams, delivering complex Manufacturing Facility and processing projects, in a highly automated GMP production environment Demonstrated capacity to effectively manage and execute projects from initiation to completion Full project lifecycle experience from end to end design through to More ❯
projects in accordance with the company project roadmap throughout the project lifecycle ensuring governance to current engineering standards and compliance with CDM regulations. Strict GMP compliance to be adhered throughout the lifecycle of the project. Coordination with the Principal Contractor and all other project team members to ensure completion to … budget and provide accurate monthly reports Attendance at daily update meetings Ensure compliance with all HSE & CDM requirements Ensuring compliance of project delivery with GMP requirements and company UKSL SOP’s Develop and updated project schedule defined appropriately according to project stage-gate Identify, record and monitor project risks, seeking … level Project Engineer/Project Manager with experience in managing cross functional teams, delivering complex Manufacturing Facility and processing projects, in a highly automated GMP production environment Demonstrated capacity to effectively manage and execute projects from initiation to completion Full project lifecycle experience from end to end design through to More ❯
To complete customer line forms, questionnaires and specification requests. To set up and maintain data in the companys ERP system(s). To undertake GMP audits according to agreed audit schedule, distribute the results and ensure the closure of actions raised. To lead and/or participate in root cause … methodical, with excellent administrative and strong communication skills. Good relationship building skills with both internal and external stakeholders. An understanding of the principles of GMP and Global Food Safety Initiatives. Personal Skills An excellent multi-tasker, able to manage multiple projects simultaneously and who thrives in a fast paced role More ❯
/office arrangement as the business requires. The role of the Senior Technical Editor is to manage the creation of new documents and revise GMP documents for complex technical changes. Key responsibilities: Independently manage the creation of new documents and revise GMP documents for complex technical changes according to documented … Tasks and CAPAs Creation and coordination of Change controls and completion of change assessments in Trackwise in conjunction with internal Lonza donors Maintenance of GMP document templates and document style and format standards Advise on document style and content, use of DMS, documentation procedures and documentation best practice and provide More ❯
/office arrangement as the business requires. The role of the Senior Technical Editor is to manage the creation of new documents and revise GMP documents for complex technical changes. Key responsibilities: Independently manage the creation of new documents and revise GMP documents for complex technical changes according to documented … Tasks and CAPAs Creation and coordination of Change controls and completion of change assessments in Trackwise in conjunction with internal Lonza donors Maintenance of GMP document templates and document style and format standards Advise on document style and content, use of DMS, documentation procedures and documentation best practice and provide More ❯
