- Senior Quality Specialist (European Locations considered)
Serve as a quality consultant to designated operational group(s) (Clinical Operations). Activities include: identification of process improvement opportunities, process authoring, and review and leadership, support for and leadership of process re-engineering
- Senior Quality Assurance Specialist / Manager, GMP – Global Pharma – North West/Cheshire, upto £50,000
We are a global Biopharmaceutical organisation offering an exciting opportunity for a seasoned Quality Assurance professional to join their team on a permanent basis.
- Senior Specialist, EMEA & APAC Human Resources Program Management Job
POSITION Senior Specialist, EMEA & APAC Program ManagementSUPERVISOR Sr Director, Talent & LeadershipDEPARTMENT Human ResourcesPREREQUISITES Min 8 year of experience in similar roleFluent in EnglishResponsibilities include, but are not limited to:• Accomplish talent and leadership objectives by planning, scheduling, organizing, monitoring, surveying and administering global Talent and Leadership Programs and interventions. ...
- Senior Quality Assurance Officer, GMP – Global Pharma – North West/Cheshire, upto £40,000 + benefits
We are a leading global Pharmaceutical and Biotechnology organisation who are looking for an experienced Senior Quality Assurance Officer to join our established Quality Assurance team.
- Pharmacovigilance Specialist with Italian
On behalf of our client, a global organisation, we are currently recruiting for Pharmacovigilance Specialists with fluent Italian.
- Document Management Specialist (experienced Trial Master File Administration)
A great opportunity for a senior level TMF (Trial Master File) team lead looking for that next step!
- URGENT - Senior QA Specialists - 9 Month Contract
Key Words: QA, Quality Asssurance, Specialists, Audits, CMO, QP, GMP, Compliance, GxP, CAPA
- Senior Clinical Trial Specialist
PAREXEL Contract Personnel Services (CPS) is currently looking for an experience Clinical Trial Specialist in Berkshire (UK), to facilitate the country and site level set-up activities for clinical trials and to support the feasibility process.This is a permanent position with PAREXEL and the successful candidate will be working on studies dedicated to one client.
- Process Technologist
Process Technologist Surrey, UK An opportunity has arisen for a Process Technologist, with a strong background in scale-up and technology transfer, within a specialist pharmaceutical company based in Surrey. This could be a great opportunity for an experienced technologist who is looking to take the next step in their career or take on a new challenge in a specialist and fast paced environment. ...
- Director of QA Compliance
We are seeking a seasoned professional to join our high growth global Clinical Research Services business unit. This is a newly established, high impact role reporting to the SVP of Clinical Research Services with global responsibility to develop, manage and enforce a robust quality function, You will serve as the primary interface with senior management regarding quality /compliance and continuous improvement, and provide consultation and recommendations to CRS functional heads.