GxPOrbis matches vetted Quality, Regulatory, Clinical and Manufacturing professionals from India with sponsoring employers across Europe and the UK — end to end, from CV to relocation.
We work exclusively in GxP-regulated pharma and healthcare — so every candidate we put forward already speaks the employer's language.
Batch release, QMS ownership, deviations & CAPA, audit readiness across GMP sites.
Analytical testing, method validation, lab compliance and instrument qualification.
Dossier submissions, MHRA/EMA liaison, labelling and lifecycle registration work.
Trial monitoring, CRA/CRO roles, GCP compliance and site management.
Case processing, signal detection, safety database and PSUR support.
Production & process engineering, tech transfer, validation and site operations.
The same pipeline, whether you're a candidate or a hiring partner on the other side of it.
Share your profile — experience, certifications, target function. We assess sponsor-eligibility honestly, upfront.
We map you to live sponsor-eligible openings and rebuild your CV/LinkedIn for the European market.
Mock interviews, employer briefings, and application support until an offer is on the table.
Contract review, visa documentation guidance, and a relocation checklist through your first day.
Every opening we send you has already been checked for sponsorship eligibility — no wasted applications.
We source and screen against your open sponsored roles, so you only see candidates who fit and are relocation-ready.
"We only pitch roles we believe you can actually get sponsored for — not everything on the market."
"One point of contact from your first message to your first day at a European site."
"We speak GMP, MHRA, EMA and QMS fluently — so your experience translates correctly."