Flexible Hybrid Contract Jobs
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Regulatory Affairs Consultant
We are looking for an experienced Regulatory Affairs Consultant to support MDR transition, risk management, and validation documentation activities within a highly regulated pharmaceutical/medical device environment. This 12‑month hybrid assignment is based in Antwerp, working 2-3 days on‑site. Key ResponsibilitiesUpdate and rewrite Risk Management...
Quality Assurance Specialist
Quality Assurance Specialist III - Manufacturing Quality OperationsLocation: Winston‑Salem, North Carolina Employment Type: 6 month Contract, Hybrid Shift: As Assigned Department: Quality Assurance / Manufacturing Quality Operations Reports To: Associate Manager, Manufacturing Quality OperationsAbout the RoleWe are seeking an experienced Quality As...
Freelance Consultant Software as a Medical Device (SaMD)
We're looking for an experienced freelance consultant to support regulatory and quality activities across a range of complex medical devices. This role suits someone who has worked with life‑sustaining, electromechanical, infusion, monitoring, renal, or surgical technologies and understands the demands of global compliance.What You'll DoDevelop reg...
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Data Engineer
Freelance Data Engineer - Medical Devices (Ireland)A leading Medical Devices organisation is expanding its digital, data and analytics capability to support next‑generation connected devices, diagnostics, and internal manufacturing intelligence platforms. We are seeking a Data Engineer who can deliver end‑to‑end solutions, from data modelling to de...
Electrical Engineer- Freelance
Job Title: Electrical Engineer - Freelance (12‑Month Contract)Location: Munich- On-site 4 days/week (Hybrid on remaining day) Department: R&D / Hardware Engineering Contract Type: Freelance / Freiberufler, 12 monthsAbout the Role12‑month freelance contract supporting advanced hardware development.Contribute to design, testing, and integration of ne...
QA Specialist Environmental Monitoring
AP QA Specialist (Aseptic Processing) - FDA ReadinessContract: 2 months, 40 hours/week Start: Immediate (FDA readiness deadline: June) Level: Mid-Senior SpecialistAbout the RoleA leading pharmaceutical manufacturer is seeking an experienced AP QA Specialist to support critical aseptic processing readiness activities ahead of an upcoming FDA milesto...