Quality Control Analyst

Company: Advanced Medical Solutions
Apply for the Quality Control Analyst
Location: Plymouth
Job Description:

Overview

This job will be the routine analysis of production materials and finished products as defined in the QMS. You will also be required to provide analytical support, where required within AMS Plymouth, this may involve support of R&D work, testing for regulatory and investigational purposes. You will also be responsible for conducting other QC/QA related functions.

Responsibilities

  • Perform routine analytical analysis on physical test methods, GC-FID, HPLC and Karl Fischer.
  • Mentor / provide guidance on Lab procedures / practices.
  • Provide analytical support to other departments within AMS.
  • Protocol & Report writing.
  • Perform viscometry, set time and tensile testing.
  • Responsible for in-process inspection and testing, and testing for final product release.
  • Responsible for recording and maintaining accurate records of inspections conducted.
  • Ensuring that Good Manufacturing Practice (GMP) is maintained at all times.
  • Supporting QA with day to day tasks.
  • Project Management.
  • Improvement Projects.
  • Any other reasonable requirement as required to meet the business objectives.
  • Chemical & performance analysis of raw materials as part of goods received inspection
  • Chemical & performance analysis of manufactured products as part of QA product release
  • Responsible for ensuring that the Device History Files are maintained.

Qualifications

  • BSc Chemistry or equivalent with 2-3 years related experience within laboratory environment.
  • Ability to write reports & effectively present information and respond to questions from AMS personnel.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Computer literacy.
  • This position requires attention to detail, and the ability to follow defined procedures. The role also requires interaction with other departments.
  • A background in an analytical / test laboratory environment, within a controlled QMS system.
  • A very thorough person, with significant attention to detail.
  • Able to work independently, but also as part of a small team.
  • Able to communicate effectively at all levels within the organisation.

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Posted: June 30th, 2026