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RP contract

RP contract

  • Location

    Slough

  • Sector:

    Quality & Validation

  • Job type:

    Contract

  • Salary:

    £50 - 60 per hour

  • Contact:

    Joe Lane

  • Contact email:

    Joe.Lane@catalystcareers.com

  • Contact phone:

    02035899282

  • Job ref:

    LM50358

  • Published:

    7 months ago

  • Expiry date:

    2019-12-10

  • Consultant:

    #

Vacancy Details

My client,  a pharmaceutical logistics company are looking for a contract RP.

Title: Responsible Person

Salary: Competitive

Location: South East

Responsibilities:

A leading highly regulated pharmaceutical organisation in the Slough area is looking for a Quality Assurance (QA) / Responsible Person (RP)

The core function of the role will be to ensure all GDP (Good Distribution Practice) activities are full compliant with regulations and Wholesaler dealing licence is retained. This is a role with responsibility covering General Medicines (Prescription) products, working on Life Cycle Management (renewals / variations) in the European Markets. Candidates will undertake the role of Responsible Person (RP) for WDA(H) – Wholesaler Dealer / Distribution Authorisation.

To be considered for the Quality Assurance / Responsible Person candidates will be registered with MHRA as a RP for WDA(H). Candidates will have understanding of quality systems and have demonstrable knowledge / experience of the Regulatory within a Pharmaceutical environment.

 

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 joe.lane@catalystcareers.com or call 0203 589 9282 for a confidential discussion about potential opportunities.

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

Catalyst Life Sciences 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

Catalyst Life Sciences 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://www.linkedin.com/in/joe-lane/

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