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Database & Data Migration Consultant
Lyon

Location: Southern France (exact site location to be discussed)Contract: 3-6 months (extension potential)Working Pattern: Primarily onsiteLanguages: Fluent French requiredOverviewWe are currently seeking experienced GMP Database & Data Migration Consultants to support a major pharmaceutical manufacturing modernization programme. The successful cons...

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Fill Operator 1 First Shift
Bedford$168 - $176 USD a day

Position SummaryOur client, an established pharmaceutical manufacturing organization dedicated to developing, producing, and supplying high-quality medicines is seeking a Fill Operator I to join its first shift manufacturing operations team. This position supports sterile production activities within a regulated pharmaceutical environment and is re...

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QC Senior Scientist Raw Materials
Portsmouth$100,000 - $114,000 USD a year

QC Senior Scientist, Raw Materials Portsmouth, NH (Onsite)We're partnering with a leading life sciences manufacturing organization that is looking to add a QC Senior Scientist to support raw materials testing and laboratory operations at its Portsmouth, NH site.This is a great opportunity for a scientist who enjoys solving technical challenges, wor...

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Selby Jennings Start Your Career In Recruitment
Regualtory Affairs Specialist
$70,000 - $90,000 USD a year

Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...

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Regualtory Affairs Specialist
$70,000 - $90,000 USD a year

Regulatory Affairs SpecialistMedical Device / Pharma | Hybrid Opportunity | Competitive Salary + BenefitsAre you a Regulatory Affairs professional looking for an opportunity to make a real impact on innovative products that improve patient outcomes?A growing healthcare organisation is seeking a Regulatory Affairs Specialist to join its expanding te...

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Software Quality engineer
Galway

Software Validation Engineer (Contract) | Galway | 12 MonthsA leading medical device manufacturer is seeking an experienced Software Validation Engineer to support manufacturing and quality systems within a highly regulated environment. This is an excellent opportunity to join a major organisation and play a key role in ensuring critical equipment ...

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