Contract Quality Engineer Jobs
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QA Automation Engineer
OverviewWe are working with a global MedTech organisation, currently scaling its Digital R&D capability.They are looking to bring in an automation-first QA Engineer (SDET) to help improve testing capability within a fast-paced, product-driven environment with rapid release cycles and high delivery demands.Key Responsibilities* Build and maintain au...
Process Engineer Equipment (12 months)
Location: Wuppertal, Germany Start: ASAPHybrid (max. 2 days/week home office)Full-timeOverviewWe are currently seeking an experienced Process Engineer to join a leading pharmaceutical/biotech organisation based in Wuppertal on a 12-month contract. This role is ideal for someone with strong expertise in process equipment rather than production opera...
C&Q Lead
CQV LeadRoleWe are seeking an experienced CQV professional to take on a leadership and oversight position within a GMP pharmaceutical project currently running behind schedule. This is a strategic role, not execution-focused, where you will act as the internal CQV lead, driving delivery through a third-party provider. You will play a key role in st...
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Cleaning Validation Consultant
Work Place: On-Site, Toulouse Project Duration: 18 Months Languages: Fluent French & English RequiredNo visa sponsorship availableOverviewWe are seeking an experienced Cleaning Validation Consultant to support a high-profile, large-scale pharmaceutical manufacturing facility. This is a full-time, on-site role within a GMP-regulated environment, fo...
Quality Engineer
Quality Enginner (Freelance) Location: Montpellier, France (hybrid)Type: Freelance, full-timeStart Date: ASAPKey ResponsibilitiesReview and assess validation, change control, risk analysis (e.g., FMEAs), software validation, and microbiological/sterilisation documentation.Support product development, new product introduction, and sustaining enginee...
QMS Specialist
The QMS Specialist works within the Quality Assurance team to support and manage the Quality Management System in a pharmaceutical manufacturing environment.The role ensures compliance with cGMP standards and regulatory requirements (Swiss, EU, FDA) and focuses on maintaining and improving key quality processes such as documentation, training, devi...