Manufacturing Engineer III
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Job Location:
Cramlington - UK
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Loud Noises (Equipment/Machinery) Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)Job Description
Job Title: Engineer III Manufacturing Engineer in Business
Job Profile Title: Engineer III Production Engineer
Direct Report To: Manufacturing Engineering Manager
Group/ Division: SUD
Career Band: 6
Position Location: Cramlington
Number of Direct Reports: 0
We aim to help customers improve global health and safety. Our 100000 team members uphold Integrity Intensity Innovation and Involvement.
Job Summary
Join the Manufacturing Engineering team focusing on improving BPC / Chambers manufacturing equipment and processes.
Support the creation and execution of procedures to cGMP Standards lead engineering projects to meet performance goals budgets and timelines.
Conduct investigations into validation failures implement corrective actions and address technical issues.
You may need to visit sister branches internationally to exchange knowledge comprising under 5% of yearly travel.
How will you get here
Education:
- Mechanical/Process/Manufacturing Engineering/Science Degree or equivalent experience in engineering or another scientific field.
Experience:
- Prior practical validation experience involving Factory Acceptance Testing Site Acceptance Testing and IQ/OQ protocols.
- Having previous experience in the pharmaceutical sector provides a benefit.
- Experience working within a regulated industry/environment is essential.
- Leading/assisting qualification project executions and close out.
- Self-motivated proactive and capable of adhering to project timelines
- Writing reviewing and implementing of project URS FAT IQ/OQ DoE & PV protocols.
Knowledge Skills Abilities:
- Proficient understanding of Quality systems in the Pharmaceutical Sector
- Proficient in Solidworks or AutoCAD is important.
- Attention to detail and ability to identify and remediate issues found during testing.
- Highly effective verbal and written skills including technical authorship.
- Proficient in Microsoft Office particularly Microsoft Word and Excel
- Understanding of cGMP for all paperwork required.
Benefits we offer:
Joining Thermo Fisher offers a competitive salary holidays annual bonuses Private Health Insurance Life Insurance and a Pension Plan. Customize your benefits with our Flexible Benefits Package.
Thermo Fisher Scientific values the individual narratives of each of our 130000 brilliant employees. Join our team and support our goal of helping customers improve the health cleanliness and safety of the world.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.
Key Skills
- Lean Manufacturing
- Six Sigma
- CNC Programming
- Lean
- Machining
- Tooling
- CAD
- CNC
- Assembly Experience
- SolidWorks
- Kaizen
- Manufacturing
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
