Naukrijobs UK
Register
London Jobs
Manchester Jobs
Liverpool Jobs
Nottingham Jobs
Birmingham Jobs
Cambridge Jobs
Glasgow Jobs
Bristol Jobs
Wales Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Validation Manager

CK GROUP
Job LocationGreat Yarmouth
EducationNot Mentioned
SalarySalary negotiable
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

CK Group are recruiting for a Validation Manager to join a pharmaceutical company at their site in Great Yarmouth on a permanent basis.The Company: Our client has over 55 years experience focused on researching and developing innovative dermatological treatments.Validation Manager Role:

  • Reviewing and approving all validation plans, protocols and reports
  • Executing cleaning validation protocols at all sites
  • Managing projects and existing installations for temperature mapping / monitoring across sites.
  • Raising and managing change controls for assigned projects.
  • Preparing, controlling, reviewing, and approving Quality documentation to align with QMS.
  • Maintaining awareness of upcoming regulatory environment.
  • Assisting other departments involved in validation activities including validation of equipment, processes, and the preparation of associated documentation.
  • Liaising with the Computer System Validation team to ensure such aspects are covered during the execution of protocols.
Your Background:The successful candidate will have;
  • Several years relevant quality experience in a pharmaceutical GxP environment.
  • Degree or equivalent in appropriate scientific discipline.
  • Experience of writing protocols, reports and executing Equipment & Facilities Validations, Cleaning Validations and Process Validations..
  • Understanding of GAMP requirements for computer systems.
  • Clear understanding of; GMP, or any other GxP area, regulatory and accreditation systems, quality management, NC/CAPA, & Change Controls.
  • Knowledge of legal framework concerning pharmaceutical manufacture i.e. Eudralex, ICH guidelines, medical device legislation.
Apply:It is essential that applicants hold entitlement to work in the UK. Please quote job reference 55101 in all correspondence.

APPLY NOW

Validation Manager Related Jobs

© 2019 Naukrijobs All Rights Reserved