QA Auditor/QA Manager (GLP/GMP) - Home Based

CK Group are working on behalf of a biotechnology/contract research organisation to recruit for either a QA Auditor or QA Manager with GMP/GLP or GCP expertise. This will be a remote based role on a permanent basis with travel UK wide required (approx 50%)

Location:
Our client has offices in the UK (North West), Australia and Singapore. They operate throughout Europe, North America, South America, Asia, Africa. This position is remote based in UK and will involve travel to and from clients on the audit schedule. They offer fantastic opportunities for personal development and advancement as well as competitive salaries, company pension scheme, private healthcare, share options, and life insurance.

QA Auditor/QA Manager (GLP/GMP) Role (depending on experience):

1. QA Auditor - Plan, organise and report internal and external audits in support of our clients audit schedule and that of other client organisations. This position will report to the QA Manager.
2. QA Manager - Develop and improve the Quality system.

QA Manager Background:

• Bachelor’s degree, or equivalent, in science.
• Strong industry QA experience preferably in a Pharmaceutical CRO (4 years+).
• Full Clean Driving licence, ability to travel up to 3 days/week (post-covid).
• Strong understanding of the clinical process (particularly Phase II & III).
• Management experience.

QA Auditor Background:

• Bachelor’s degree, or equivalent, in science.
• GMP or GLP auditing experience within a pharmaceutical/clinical trial environment (2 years+) of planning, performing and reporting an audit.
• Strong understanding of the clinical process.
• Full driving licence and a willingness to travel (50%).

Apply:
For more information or to apply for this QA Auditor/QA Manager (GLP/GMP) position, please contact Naynesh on 01246 457703 or email nmistry@ckgroup.co.uk, quoting job ref 50781.

It is essential that applicants hold entitlement to work in the UK.

INDGEN