Process Engineer
Global Pharma Tek
Process Engineer
The Process Engineer participates in Operations, and Engineering initiatives. Directly responsible for supporting assigned manufacturing processes along with supporting new implementations. This position will be working closely with all aspects of the business as cross functional support.
Responsibilities:
- Support Operations team with Setup and Operation thin metal stamping and forming processes.
- Develop Work Instructions to standardize setup and operations
- Identify and implement improvements in the existing equipment/tooling in assigned area.
- Support new equipment / process implementation and transfer of equipment/processes.
- Lead equipment maintenance efforts including, developing preventative maintenance activities and intervals.
- Support Design for Assembly analysis.
- Risk Analysis Activities
- Product Validation Activities
- Continuous improvement Activities
- Support tooling maintenance and repair activities
Special Requirements or Call outs:
Other Requirements (Specialized):
- Metals Processing:
- Stainless steel film stamping
- Stainless forming and winding
- Custom Built Equipment
- Electro-Mechanical troubleshooting and improvement of systems in production
- Precision alignment or adjustment +/- 0.00X" of mechanical assembly systems
- Pneumatic, PLC
Transportation/Parking Information:
Parking is at the client site – no public transportation
Recruitment Focus Areas:
Sarasota, FL
Conversational / Qualifying Questions:
Need to have experience with "older" mechanical equipment – metal stamping or forming
Assignment Type:
Temp-to-hire (potentially) 12-18 months
Hours:
Flexible – training will be 6a-230p but shift will be 130p-1030p
Is OT required:
Potentially
PPE/Dress code:
N/A
Talent Factory Delivery & Overfill:
Internal submission to Matt – interviews will follow
Interviews:
"Teams" interview followed by in person/site visit
Next Steps:
Orientation is the first day on assignment
Education/Certification Requirements:
Educational Qualifications: Bachelor's Degree in Engineering discipline or equivalent tool and die, metal stamping, or metal forming is required.
Experience requirements:
- 3 to 5 years' experience in medical device manufacturing environment.
- Relies on limited experience and judgment to plan and accomplish goals.
- Lean manufacturing and advanced statistical analysis.
- CAD / Drafting Experience. Solidworks
- Computer literacy, knowledge of Microsoft Windows, Microsoft Office.
- Understanding of Bill of Material (BOM).
- Capable of creating drawings, manuals, and engineering specifications.
- Self-starter with enthusiasm and ability to work in a team environment.
- Familiarity with ISO standards, GMP, and OSHA regulations.
- New Process Development
- PFMEA Development Leader
- Process DOE development and execution
- Process Validations
Assessments Needed:
N/A
Background Exception (Y/N):
N
Do Not Return List? (Yes/No):
Y
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