QC Coordinator

QC Coordinator
  • Competitive
    ANNUM
  • Permanent
  • Livingston, West Lothian, Scotland, UK EH53 0TG Livingston West Lothian UK EH53 0TG
Job Ref: J2157542
Sector: Science
Sub-sectors: Biotech/Life Sciences, Pharmaceuticals
Date Added: 15 October 2020
A leading pharmaceuticals company are looking for a QC Coordinator to join their growing team in Livingston.

QC Coordinator

Livingston

Permanent Opportunity

Competitive Salary

The Company

A leading pharmaceuticals company are looking for a QC Coordinator to join their growing team in Livingston. The company are a cGMP facility working on a range of products for the global market.

Now is a great time to join this expanding company who have a great reputation.

The Role

The successful QC Coordinator will work within the company's QC team on a range of duties in a cGMP environment. Reporting to the Lab Manager you will be responsible for QC sample logistics, including shipments. The role would be suited to someone with previous experience in a QC position who has worked in a GMP/GLP environment. Key responsibilities include;

  • Shipment of QC samples and materials to approved suppliers
  • Act as SME for shipments and provide training in process for others
  • Act as central point of contact for receipt of certificates
  • Support co-ordination of the storage of QC samples and sample logistics for all testing
  • Working with Raw Materials Coordinator, maintain raw material specifications to ensure continued compliance, acting as their deputy as required
  • Immediately escalate and report any deviations to materials, facilities, processes or procedures to line manager and progress QMS in a timely manner
  • Maintain all QC systems, databases, logs and support the generation of QC trend data
  • Support QC activities in line with manufacturing schedule, as per rota. This includes provision of overtime cover as required
  • Shift work and out of hours work as required

Your Experience

The successful applicant will have the following skills/experience;

  • A BSc or above in a relevant scientific subject
  • Experience in raw material testing and sample management and shipping as well as managing external relationships effectively.
  • Experience working in a GMP environment and working to deadlines, managing conflicting priorities.

Next Steps

If you are looking to become a QC Coordinator for a leading pharmaceuticals company in Livingston please apply online. Any queries can be directed to Luke on 0141 847 0319 or luke.argent@srgtalent.com

SRGTalent
14/11/2020 17:24:22
GBP 0.00 0.00
Contact Consultant:
Luke Argent

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