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QA Specialist with GLP

QA Specialist with GLP

Job Title: QA Specialist with GLP
Contract Type: Contract
Location: Bedfordshire
Industry:
Salary: Negotiable
Start Date: ASAP
Reference: CW-QA_1487839884
Contact Name: Catherine West
Contact Email: c.west@sciproglobal.com
Job Published: February 23, 2017 08:51

Job Description

I am currently working with a Pharmaceutical Company that is seeking a QA Specialist with a strong background in GLP. You will need to have a minimum of 2 years experience in a QA environment.

Responsibilities include:

  • To assure that regulatory studies are performed in compliance with GLP.
  • To conduct timely and effective inspections of critical study phases according to company Standard Operating Procedures.
  • To investigate deviations from Plans or SOPs (including the review of any corrective and preventative actions required) and to advise scientific staff and Management accordingly.
  • To act as a contact for Quality Assurance GLP enquiries and to advise staff of the specific regulatory requirements as appropriate (recommending suitable solutions where necessary)
  • To write and/ or test out proposed and modified QA SOPs with the object of assessing effectiveness and practicality

Sounds like something you'll be interested in? Please get in contact, call me on 02033273072 or email me at c.west@sciproglobal.com