QA advisor

Recruiter
JCW Search Ltd
Location
Ely
Posted
16 May 2018
Closes
15 Jun 2018
Contract Type
Permanent
Hours
Full Time
Vacancy Details

My client, a global, analytical laboratory service provider, based in Cambridgeshire are seeking a QA advisor. They are a world-class bioanalytical capability with more than 50 years' experience in high-integrity analytical science and expertise spanning small and large molecules, biomarkers, molecular biology and microbiology including surveillance.The ideal candidate must have GCP / GLP experience and at least 5 years working in Quality Assurance.

Title: QA advisor

Salary: up to £43K

Location: Cambridgeshire

Responsibilities:

* Plan, coordinate and execute audits and maintain the Quality Management system
* Supervise or mentor other Quality Advisors
* Maintain a strong knowledge in the current regulations and guidance
* Support external inspections and customer enquires
* Actively seek improvements wherever possible
* Lead the development and delivery of training modules

Candidate requirements:

* Candidates must have strong experience in Quality Assurance within a regulated GLP/GCP environment within an analytical laboratory
* You will be able to communicate effectively with all areas of the business
* You will be highly organised and methodical
* You will demonstrate an analytical and meticulous approach to tasks, working both independently and as part of a team
* You will actively seek to process improve wherever possible.

Looking but this isn't the right position for you?

If you are interested in a new opportunity but your experience doesn't fit this role, please email your CV or call [Phone number removed] for a confidential discussion about potential opportunities.

NOT OF INTEREST TO YOU BUT KNOW SOMEONE IT WOULD BE?

JCW offer a generous referral scheme reward, whereby anyone who refers us to a successfully placed candidate is entitled to up to £250 worth of vouchers.

JCW

JCW are a global recruitment company operating in the Life Sciences space, with specialist consultants working within the technical and regulatory areas. This includes the following markets;

* Pharmacovigilance/Drug Safety
* Regulatory Affairs
* Quality Assurance
* Quality Control
* Medical Information
* Medical Writers
* Medical Affairs
* Compliance
* Audit
* Validation
* Production
* Manufacturing
* Clinical Trials
* Clinical Research
* Project Management
* Finance

My Linked In Profile

https://[URL removed]

I personally specialise in recruiting QA and validation professionals for roles across the UK so please do get in touch should you be considering new roles, or looking to fill ones at your current company!

KEYWORDS

GMP / GLP / GCP / PV / Drug safety / CRO / regulatory / pharmaceutical / analytical / Cambridge /
This job was originally posted as www.totaljobs.com/job/81445858

Similar jobs

Similar jobs