SonicJobs Logo
Left arrow iconBack to search

Manufacturing Quality Engineer – Leicester

Inizio Engage
Posted 2 days ago, valid for 8 days
Location

Leicester, Leicestershire LE1 4PG, England

Salary

£50,000 - £55,000 per annum

Contract type

Full Time

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.

Sonic Summary

info
  • This position is for a Quality Engineer transitioning from industries like Automotive or Aerospace to the pharmaceutical sector.
  • Candidates should possess an MEng in Mechanical, Automotive, Aerospace, or a related field, with industrial experience as a Quality Engineer.
  • The role involves providing technical reviews and input on equipment and facilities, along with QA responsibilities for various specifications and procedures.
  • The company is looking for someone who can assist in creating change controls and conducting CAPA clinics for the engineering team.
  • The salary for this position is competitive, reflecting the candidate's experience and qualifications.

This is a unique opportunity for a Quality Engineer to transfer their skillset from more conventional industries, such as Automotive and Aerospace, into an equally regulated pharmaceutical industry.

Our client is expanding rapidly and has a small in-house team of design engineers, machinist and welder, control engineers, service engineers and building systems and maintenance engineers. They are looking for a Quality Engineer to join their Quality Assurance department to act as the primary liaison with the engineering team.

You will need a good foundation in engineering disciplines and will be provided training in the relevant pharmaceutical disciplines.

Key responsibilities

  • To provide technical, engineering review and input into the design, build and maintenance of equipment and facilities. This includes, but is not limited to:
    • Providing QA review of User Requirement Specifications, Functional and Design Specifications, FAT and SAT.
    • Assisting with creating Change Controls.
    • Assisting with creating, and providing QA review, of calibration certificates generated in-house.
    • Creating User Requirement Specifications for the engineering team when the driver is improvement in quality (e.g. to accommodate a change in the pharmaceutical regulations).
    • Providing QA review of engineering Standard Operating Procedures, ensuring the process is as described and suitable.
    • Providing QA Go/No Go decisions for engineering.
  • To run CAPA clinics for the engineering team to help the team close out overdue actions on QIs and Deviations and help generate and keep updated progress on planned Change Controls.
  • To provide Subject Matter Expertise in investigations that requires engineering knowledge, collate supporting information from the engineering team and complete Risk Assessments on the impact of engineering QIs and Deviations.
  • To provide technical, engineering review and input to the Validation Team during IQ/OQ.

Experience & Qualifications

  • MEng in Mechanical, Automotive, Aerospace, or similar. The role requires a broad foundation in understanding of basic engineering disciplines:
    • Materials and Structures.
    • Pressure and Flow.
    • Heat Transfer.
    • Mechanisms and Control.
  • Specialism in material identification and fractography preferable.
  • Industrial experience as a Quality Engineer and experience with Quality Management Systems.

Apply now in a few quick clicks

By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.