JT587 - MANUFACTURING ENGINEER II
Most applications go out cold — see where you stand first. No sign-up to start.
Don't just apply. Show up ready.
Olive works from this exact posting — no sign-up to start.
At a glance
Requirements
Credentials this posting asks for.
Job overview
Quality Consulting Group is hiring a JT587 - MANUFACTURING ENGINEER II. Quality Consulting Group is seeking a highly motivated Manufacturing Engineer II to join their team in the pharmaceutical, biotech, medical devices, and manufacturing industry. This role involves contributing to a world-class manufacturing environment in Puerto Rico and the USA, working with an enthusiastic team.
Key focus areas include Design manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling., Design arrangement of machines within plant facilities to ensure most efficient and productive layout., and Design sequence of operations and specify procedures for the fabrication of tools and equipment and other functions that affect product performance..
Successful candidates bring Bachelor's Degree In Engineering and 3+ Years Of Relevant Experience. Important skills include Process Development, Equipment Validation, SOP Development, Special Build Documentation, Line Support, and Equipment IQ.
Skills & qualifications
Skills
Qualifications
Full job description
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
-
Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
-
Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
-
Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
-
Adapts machine or equipment design to factory and production conditions.
-
May incorporate inspection and test requirements into the production plan.
-
Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
-
Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.
Qualifications:
-
Bachelor’s degree in Engineering
-
3+ years of relevant experience.
-
Process Development and documentation
-
Equipment validation
-
SOP Development
-
Special Build Documentation and Line Support
-
Experience in equipment IQ |Experience in OQ (Operational Qualification) and PQ (Performance Qualification) and/or process validation
-
Process Validation Lifecycle ( from process characterization, operational qualification to performance qualification)
-
SOP Development | Special Build Documentation and Line Support
-
Computer and software validation CSV
-
Change control of Medical Devices
-
MES system
-
Experience in injection molding processes
-
Shift: 1st shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Powered by JazzHR
You've read the whole posting — now see how you match it.