6 of 6 Remote/Hybrid Permanent GMP Jobs

Profile Essential ~5 years’ experience in pharmaceutical or medical device manufacturing Background in production, process engineering, or quality Strong understanding of manufacturing operations in GMP environments across multiple products and processes. Excellent communication and problem-solving skills Desirable Exposure to MES or manufacturing digitalisation initiatives Quality Assurance, process improvement ...

system rules. Familiarity with relational databases. Experience with DC schemes. Experience with buy-in/buyout data requirements. Exposure to pensions projects such as GMP Equalisation or Pensions Dashboard. What you can expect in return A competitive salary and market leading bonus scheme with stretch targets for high performance Study ...

system rules. Familiarity with relational databases. Experience with DC schemes. Experience with buy-in/buyout data requirements. Exposure to pensions projects such as GMP Equalisation or Pensions Dashboard. What you can expect in return A competitive salary and market leading bonus scheme with stretch targets for high performance Study ...

agency or client side). Highly organised, calm under pressure and confident communicating performance insights. Experience in lead generation, Google Ads/Microsoft Ads, GMP or Meta Blueprint is an advantage. Why Join Us: Competitive Salary 31 days holiday, increasing to 33 days after 2 years of service plus have ...

Document Management System (DMS) in preparation to a migration to Veeva Vault system. This role is critical to ensuring documentation related to GMP manufacturing processes is current, compliant, and readily accessible. The System Specialist will support cleanup activities related to the DMS, manage the review and approval workflows of global … Periodic Review Monitoring: Track, monitor and update the Past Overdue Periodic Review Reported, and create monthly reports of periodic document reviews in accordance with GMP and internal procedures. Escalate overdue tasks and non-compliance issues to department leads and Quality leadership. • Translation Coordination: Oversee the translation of controlled documents ...

PAYE | £42 UMB Overview: We’re looking for a detail-oriented System Specialist to manage and support our Document Management System (DMS) within a GMP pharmaceutical environment. This role will focus on document lifecycle management, system coordination, and supporting a migration to Veeva Vault. Key Responsibilities: Manage … validation docs) Act as DMS Super User: workflows, permissions, master data, and reporting Support DMS cleanup and migration activities Monitor periodic reviews and ensure GMP compliance Coordinate document translations across global teams Provide user support, training, and troubleshooting Requirements: Degree in Life Sciences or related field 3+ years in document ...