CQV Lead

Up to US$80.00 per annum
  1. Contract
  2. Validation
  3. United States
Topeka, Kansas
Posting date: 20 Feb 2019

ProClinical is advertising a vacancy for a CQV Lead with a global engineer consultation company. This organisation is offering an exciting opportunity for an experienced CQV consultant to provide leadership and management to an existing filing line. This is a contract role, running for an initial 3-6 month duration, with a possibility to extend.

Job Responsibilities:

  • Developing a validation Master Plan.
  • Increasing company production.
  • Working with CQV equipment.
  • Executive all CQV deliverables.
  • Ensuring timely approval of all Commissioning and Final Reports.

Skills and Requirements:

  • Demonstrable experience with Front Identification and Design Scope.
  • Experience with conceptual designing.
  • Experience with cleaning and dirty steam.
  • An ability to learn, assimilate, and effectively communicate information to support colleagues, discuss with partners, and advise clients on requirements.
  • Strong interpersonal skills, including communication, leadership, relationship management, and influencing.
  • Capable of leading interdisciplinary projects and to implement change within a high-performing organisation.
  • Demonstrable computer software skills, including MS Office.
  • A flexible mindset that is suited to dealing with multiple projects in a timely manner.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Keri Marshall on +44 207 440 0679 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.