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13485 - QA/RA manager

13485 - QA/RA manager

  • Location

    Greater London

  • Sector:

    Quality & Validation

  • Job type:

    Permanent

  • Salary:

    £45k - 60k per year

  • Contact:

    Cheikh Khoule

  • Contact email:

    Cheikh.Khoule@jcwresourcing.com

  • Contact phone:

    02035899300

  • Job ref:

    LM49498

  • Published:

    8 months ago

  • Expiry date:

    2019-11-13

  • Consultant:

    #

Vacancy Details

My client, a Global medical devices company based in Greater London are looking for a 13485 - QA/RA manager.

A great opportunity to join an expanding team with a great portfolio of products.

 

13485 – QA/RA manager

Location: Greater London  

Salary: Up to £60,000

Duration: Permanent

Job function:

  • Taking responsibilities for quality and regulatory strategies
  • Leading Quality and regulatory team
  • Taking responsibility for 13485 and FDA compliance
  • Being the liaison with autorithuies and notified bodies
  • Taking responsibilities for clients and 3rd party audits
  • Promoting awareness regulatory to the organisation

 

To be considered you need to have;

  • Eligibility to work in the UK and travel in EU
  • 4+ years Quality management in 13485 regulated industry
  • Excellent communication and writing skills
  • Strong auditing experience desirable
  • Experience dealing with senior stakholders

 

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 to cheikh.khoule@catalystcareers.com or call 0203 589 9296 for a confidential discussion about potential opportunities.

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

CLS 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.

Catalyst Life Sciences

CLS 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

linkedin.com/in/cheikh-khoule

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

KEYWORDS

13485 / medical / devices / production / GMP / audit /manufacturing / quality / QA / RA / regulatory / 9001 / report / MHRA / FDA / 5001 / QMS /