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Quality Inspector

Prime Appointments
Posted 5 hours ago, valid for 12 days
Location

Saxmundham, Suffolk IP17, England

Salary

£35,000 per annum

Contract type

Full Time

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Sonic Summary

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  • The role of Quality Inspector is available immediately in Saxmundham, Suffolk, offering a salary of £35,000, which is negotiable.
  • The position requires experience in maintaining high standards in production and compliance with ISO 13485, ISO 9001, and FDA regulations.
  • Key responsibilities include performing inspections of raw materials and finished products, as well as supporting continuous improvement initiatives.
  • Candidates should possess strong attention to detail, excellent communication skills, and preferably have experience in a medical, biotech, or manufacturing environment.
  • Benefits include an annual salary review, a quarterly profit share scheme, and starting with 23 days of annual leave.

Role: Quality Inspector
Start date: Immediate
Location: Saxmundham, Suffolk
Hours: 07:15-16:30, Mon-Thurs with a half day finish on Fridays
Salary: 35,000 (negotiable)

A market-leading manufacturer is looking for a Inspector to join its growing Quality team. This is a hands-on role focused on maintaining high standards across the production process, ensuring compliance with ISO 13485, ISO 9001, and FDA regulations.

You'll be responsible for incoming, in-process, and final inspections, working with production & engineering to ensure only the highest quality products are released. Ideal for someone with a sharp eye for detail and a passion for improvement within a regulated environment.

Key Responsibilities:

  • Perform mechanical, physical, and visual inspection of raw materials, in-process parts, and finished products
  • Approve components and products against specifications and documented standards
  • Maintain and input accurate inspection records into the database
  • Support root cause analysis and continuous improvement initiatives
  • Conduct equipment calibration checks and maintain sterility management requirements
  • Communicate findings clearly with production and engineering teams
  • Assist in staff training on assurance processes and techniques

Requirements:

  • Knowledge of ISO 9001, ISO 13485, and cGMP/FDA systems
  • Strong attention to detail with the ability to interpret technical drawings and specifications
  • Excellent communication skills
  • Experience with inspection tools and documentation processes
  • Able to work independently and manage daily tasks with minimal supervision
  • Previous experience in a medical, biotech, or manufacturing environment preferred

Desirable:

  • Previous lab or microbiology experience
  • Understanding of sterilization processes and wound care/diagnostic products
  • Familiarity with non-conformance reporting and root cause investigations
  • Exposure to regulated industries (e.g. medical device manufacturing)
  • Proficiency in Microsoft Office and quality databases

Benefits:

  • Annual salary review
  • Quarterly profit share scheme
  • Starting 23 days annual leave
  • Dental scheme
  • Overtime paid at increased rates

For any questions, please contact Carl @ Prime Appointments, I look forward to hearing from you.

#SUFFOLKPERM

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