Part of Phaidon International
Part of Phaidon International
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Senior Quality Engineer (Integration Programme) Location: Belfast, Northern Ireland (On-Site)Contract Length: Up to 24 MonthsHours: Full-time (40 hours per week)Start Date: ASAP ResponsibilitiesAssess the acquired site's quality system, engineering processes and manufacturing controls against standards and identify integration requirements.Perform...
9-Month Initial Contract | Strong Likelihood of Extension Full-Time (37.5 hours per week) On-Site Preferred: 4-5 Days per Week in North Devon Start Date: September (Preferred)Please note: Applicants must have full right to work in the UK at the time of application. Unfortunately, we are unable to provide visa sponsorship or support visa transfers f...
9-Month Initial Contract | Strong Likelihood of Extension Full-Time (37.5 hours per week) On-Site Preferred: 4-5 Days per Week in Ilfracombe Start Date: September (Preferred) We are seeking a Customer Interaction Officer (CIO) to join a busy and highly collaborative Customer Complaint Handling team. This role sits at the heart of the customer exper...
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OverviewWe are seeking an experienced QA Qualification / Validation Engineer to join a highly regulated pharmaceutical manufacturing environment. This role provides Quality Assurance oversight for qualification, validation, commissioning, and lifecycle management activities related to manufacturing systems, process equipment, laboratory equipment, ...
Location: Belgium (Beerse / Ghent) Contract: Freelance Consultant Industry: Pharmaceutical & Biotechnology OverviewWe are supporting multiple strategic programmes within a global pharmaceutical environment and are looking to engage experienced QA-CSV, Digital Compliance and Computerised Systems Validation professionals.Opportunities are available a...
OverviewWe are seeking experienced quality professionals to support a major pharmaceutical manufacturing client in Greenville, North Carolina. This engagement focuses on strengthening quality oversight, manufacturing compliance, remediation activities, and inspection readiness efforts within a regulated GMP environment.Consultants will join an esta...