Cpl jobs - Life science tower Jobs in Down, Ireland

Clinical operations manager

LondonCpl

CPL Life Sciences are actively hiring in collaboration with a London based Academic research trust for a Clinical Operations Manager on a 12 month contract. 12 month contract initially Hybrid based Line management responsibilities Oncology focused Operational management UK and EU experience idealThis senior role sits within a [...]

Category Banking, Insurance, Finance & Accountancy

1 day ago in TechSkills

Head of quality operations/responsible person

DublinCpl

...those products.Requirements:· Pharmacy or Analytical Science or related· 10 years’ experience in Pharmaceutical Industry· Ability to work in a complex matrix team environment and with both internal and external partners· Currently listed as Responsible Person (RP) on Irish licenceFor a full Job Spec and to apply for [...]

Category Banking, Insurance, Finance & Accountancy

2 days ago in Experteer

Salesforce technical architect

DublinCpl

...Services, Wealth, Public Sector, Life Sciences, or Communications and Media to translate complex business requirements into scalable Salesforce platform solutions.• Operate as a trusted advisor to senior client stakeholders including Enterprise Architects and senior leadership teams.• Collaborate with cross functional [...]

Contract Type: Freelance
Category Fashion & Arts

3 days ago in TechSkills

Product manager medical devices

DublinCpl

...and product improvements. Product Lifecycle Management · Oversee assigned product lines from concept to post-market support. · Manage product documentation, clinical claims, and technical information in collaboration with R&D and Regulatory Affairs. · Support MDR and MDSAP readiness by ensuring product data, IFUs, and [...]

Category Office & Administration

5 days ago in Experteer

Product manager medical devices

DublinCpl

...and product improvements. Product Lifecycle Management · Oversee assigned product lines from concept to post-market support. · Manage product documentation, clinical claims, and technical information in collaboration with R&D and Regulatory Affairs. · Support MDR and MDSAP readiness by [...]