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QC Officer

  • Location

    Merseyside

  • Sector:

    Pharmaceutical & Chemical

  • Job type:

    Permanent

  • Salary:

    Salary Negotiable DOE

  • Contact:

    Lara Boggan

  • Contact email:

    larab@scantec.co.uk

  • Contact phone:

    +44 (0)151 666 8999

  • Job ref:

    LB151021QC

  • Published:

    29 days ago

  • Expiry date:

    2021-12-05

  • Start date:

    2021-10-15

Role: QC Officer 
Full time/Permanent – Northwest  
Contractual hours of work are 37.5 hours a week 
Salary - DOE  

This role has come about due to rapid growth, and it’s a very exciting time to join the team.  
Do you want to feel inspired every day?  Be part of a company that what to succeed together through passion, commitment, and teamwork?  
Lots of opportunities to really develop your career within a stable and growing business, rewarded with a competitive salary. This role will report directly to QC Manager 

Duties will include: 
  • QC laboratory set up programs to include design, build-out, transfer and qualification of essential equipment and assays.  
  • QC approval at all stages of the manufacturing process.  
  • Design and implement assay qualification protocols.  
  • Key point of contact for contract analytical laboratories.  
  • Ensure continued maintenance and qualification of QC facilities, equipment and assays. Manage the timelines to ensure briefs can be delivered in time right first time.  
  • Maintaining and calibrating measuring equipment to various testing standards  
  • Questioning the nature of defects while providing future solutions  
  • Alerting the Quality Assurance department of ongoing problems and delivering resolutions  
  • Inspecting raw materials to ensure consistency and integrity 
  • Filling out and maintaining proper paperwork 
To be considered for this role, candidates are required to have:  
  • Successful candidates will have previous experience of working in quality control within a pharmaceutical GMP environment.  
  • Good working knowledge of Good Manufacturing Practice for IMPs (Annex 13) Standard Operating Procedures and MHRA guidelines.  
  • Significant experience working within Pharmaceutical QC. 
  • Solid working knowledge of GMP & QC related pharmaceutical regulations & standards.  
  • Experience of having worked in an IMP Manufacturing environment preferable.  
  • Computer literate (Word, Excel, MS Office)  

To apply please forward your details for immediate consideration.  




Scantec Personnel Limited is acting as an employment business and an employment agency. For contract or interim roles (and unless otherwise stated), all pay rates stated are on a Limited Company basis. Agency PAYE, Umbrella and CIS (if applicable) engagement models are also available, which will result in a different pay rate than advertised above.

 
 
Due to the high volume of applications Scantec receives it is not always possible to acknowledge every application. Shortlisted applicants will be contacted within 28 days. If you don’t hear from us within 28 days your application has not been shortlisted at this time, to be considered for future vacancies please register with us on our website.