Qc Manager

☞ ClickJobs.io

View: 107

Update day: 03-06-2024

Location: Runcorn North West

Category: Quality Assurance / Quality Control

Industry: Human Resources Services

Position: Mid-Senior level

Job type: Full-time

Loading ...

Job content

QC Manager // Permanent // Pharma - OSD // North West Our client is based in Runcorn and manufactures and packs tablets and hard-shell capsules for the nutritional industry and has an annual turnover of circa £65m. they are currently looking for a QC Manager to join their growing operation on-site in Runcorn. The company employs circa 350 people and has an excellent track record of growth and ambitious plans for future expansion. As a QC Manager, you will you will ensure all analytical instrumentation is calibrated and maintained to GMP standards and provide technical support to the QC team and other business functions wherever necessary. Responsibilities:
  • Oversee the running of the QC laboratories and functions including raw materials, finished products, stability and method validation
  • Work closely with other departments managing expectations and transfers of internal projects
  • Ensure all analytical instrumentation is calibrated and maintained to GMP standards
  • Support in the timely release of raw materials and finished products
  • Provide technical support to the QC team and other business functions where necessary
  • Develop departmental KPIs to accurately monitor performance
  • Ensure the cleanliness and tidiness of the work area and to ensure a standard of good housekeeping in all areas of the Company.
  • Continually assess QC business risk associated with the QC department
  • Where necessary develop and document justifications for investment or resource changes. Person Specification:
  • BSc equivalent or higher in a science based subject
  • Experience within a highly regulated sector such as food, pharma, medical devices
  • Line management experience
  • Good communicator, to build effective relationships with other departments
  • Methodical, organised and have an excellent attention to detail
  • Experience of working using analytical instrumentation such as HPLC, ICP
  • Experience of test method validation and managing stability programs
  • Knowledge of EU quality related pharmaceutical and food regulations If this sounds like you, or you’d like some more information before you decide, please do feel free to reach out with a message or call along with your application! Kyle Greenwood @ Adepto Technical Recruitment
Loading ...
Loading ...

Deadline: 18-07-2024

Click to apply for free candidate

Apply

Report job
Loading ...
Loading ...

SIMILAR JOBS

Loading ...
Loading ...