Scotland Based GxP Specialist

Job Type: permanent
Salary: Competitive
Posted: March 29, 2017
Ref: SESL/2017/GCPGXP

As a head hunter for the most high end professionals in Quality assurance I have partnered up with a well-established Biotech company based in the UK, this role is ideal for anyone who wants to have a personal effect on a company and help it expand as it grows fast as the years go on! I am in search of people with great experience and knowledge with Good clinical practice (GCP). My client specialises in neurodegenerative disease research. Shortlists for applicants are being made now!

Responsibilities will include:

  • Assists in implementing a comprehensive GCP compliant quality Programme alongside assisting annual audits.
  • Assists in setting the internal annual audit schedule.
  • Oversight of contract Auditors, providing first line of communication.
  • Manages corrective and preventive action plans and follow up via an appropriate

System and/or database.

  • Assists the Head of QA coordinates Regulatory Authority TauRx facility GCP

inspections and provide assistance for other GxP Inspections.

  • Assists the Head of QA with the initiation, writing, review, approval, update and

distribution of TauRx documents e.g. policies, standard operating procedures, work

instructions and templates to support the Company Quality Management System

(QMS).

Applicants for this role are required to have

  • 10 years of relevant pharmaceutical background and strong knowledge and experience with GCP (good clinical practice)
  • Must be able to demonstrate a high standard of work and be an efficient team member.
  • At least 8 years of direct quality assurance experience.

 

Contact me today to speak more about this role and many more, to move forward in applications and take the next step in your career on:

E-mail: ssalmon@barringtonjames.com

Tel: +44 (0)1293776644

About Your Consultant

Email: ssalmon@barringtonjames.com Telephone: 01293 776644

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