Manufacturing Engineer - (Biotech)
Nesco Resource ·nescoresource.com
Apply direct
Role Overview:
Responsible for the development of manufacturing methods to produce sophisticated technology products. Works under the direction of the Manufacturing Engineering Manager developing new processes, layout optimization -supporting validation activities ensuring manufacturing requirements, cost, quality, and timing expectations are met.
Responsibilities:
• Equipment installation and validation activities (URS, FDS, IQ, OQ, PQ, and VRA)
• Cleaning validations (IQ, OQ, PQ)
• Coordinate the arrangement of machines within plant facilities to ensure most efficient and productive layout.
• Working on capital projects including financial justifications, monitoring spend
• Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts,
components, sub-assemblies and final assemblies.
• Estimates manufacturing cost, determines time standards, and makes recommendations for tooling and process requirements
of new or existing product lines.
• Maintains records and reporting systems for coordination of manufacturing operations.
• Interface with Design Engineering, Quality Engineering, Production Supervision, Tool & Die, and Machine Maintenance with
respect to manufacturing method, tooling, and equipment.
• Conduct investigations, identify, and implement corrective and preventative actions, support the appropriate disposition of
material by providing engineering inputs under general supervision in conjunction with the Quality group.
• Works with cross functional teams to develop Process Maps, pFMEA, MSA and/or other risk analysis tools
• Demonstrates courage in bringing forward new ideas and seeing them through to completion.
• Ability to make impactful Power Point presentations
• Performs other duties as assigned by the Manufacturing Engineering or Project Manager.
Location:
• Memphis, TN
Education:
• BS Engineering required
• MS Engineering a plus
Experience:
• 3-4 years with a BS degree or
• Experience with equipment installation and validation activities (URS, FDS, IQ, OQ, PQ, and VRA).
• Experience with CNC machining and validations (IQ, OQ, PQ).
• Experience with SAP and or Windchill for production routers and bill of material /change notice set up.
• Experience with AutoCAD/Draftsight/NX or similar software
• Working knowledge of metal finishing process including bead blasting process
• GD&T knowledge and experience
• Experience/knowledge with process characterization, analysis, control and validation utilizing statistical tools (Six Sigma
methodologies and experience)
• Materials experience/knowledge with manufacturing using (all or some):Titanium, Cobalt Chrome, Stainless Steels, medical
grade plastics, etc. process
• Experience working on continuous improvement projects
• MS Power Point a must
• Medical Device industry experience is a plus
Competencies:
• Design experience with product, fixturing, gauging, tooling, etc.
• Has a strong Drive for Results and acts with appropriate sense of urgency.
• Respects and values differences; takes advantage of differences to optimize results.
• Demonstrates empathy and respect.
Physical Demands:
Requires lifting up to 25 pounds up to 1/3 of the time.
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Responsible for the development of manufacturing methods to produce sophisticated technology products. Works under the direction of the Manufacturing Engineering Manager developing new processes, layout optimization -supporting validation activities ensuring manufacturing requirements, cost, quality, and timing expectations are met.
Responsibilities:
• Equipment installation and validation activities (URS, FDS, IQ, OQ, PQ, and VRA)
• Cleaning validations (IQ, OQ, PQ)
• Coordinate the arrangement of machines within plant facilities to ensure most efficient and productive layout.
• Working on capital projects including financial justifications, monitoring spend
• Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts,
components, sub-assemblies and final assemblies.
• Estimates manufacturing cost, determines time standards, and makes recommendations for tooling and process requirements
of new or existing product lines.
• Maintains records and reporting systems for coordination of manufacturing operations.
• Interface with Design Engineering, Quality Engineering, Production Supervision, Tool & Die, and Machine Maintenance with
respect to manufacturing method, tooling, and equipment.
• Conduct investigations, identify, and implement corrective and preventative actions, support the appropriate disposition of
material by providing engineering inputs under general supervision in conjunction with the Quality group.
• Works with cross functional teams to develop Process Maps, pFMEA, MSA and/or other risk analysis tools
• Demonstrates courage in bringing forward new ideas and seeing them through to completion.
• Ability to make impactful Power Point presentations
• Performs other duties as assigned by the Manufacturing Engineering or Project Manager.
Location:
• Memphis, TN
Education:
• BS Engineering required
• MS Engineering a plus
Experience:
• 3-4 years with a BS degree or
• Experience with equipment installation and validation activities (URS, FDS, IQ, OQ, PQ, and VRA).
• Experience with CNC machining and validations (IQ, OQ, PQ).
• Experience with SAP and or Windchill for production routers and bill of material /change notice set up.
• Experience with AutoCAD/Draftsight/NX or similar software
• Working knowledge of metal finishing process including bead blasting process
• GD&T knowledge and experience
• Experience/knowledge with process characterization, analysis, control and validation utilizing statistical tools (Six Sigma
methodologies and experience)
• Materials experience/knowledge with manufacturing using (all or some):Titanium, Cobalt Chrome, Stainless Steels, medical
grade plastics, etc. process
• Experience working on continuous improvement projects
• MS Power Point a must
• Medical Device industry experience is a plus
Competencies:
• Design experience with product, fixturing, gauging, tooling, etc.
• Has a strong Drive for Results and acts with appropriate sense of urgency.
• Respects and values differences; takes advantage of differences to optimize results.
• Demonstrates empathy and respect.
Physical Demands:
Requires lifting up to 25 pounds up to 1/3 of the time.
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Frequently asked questions
Who is hiring for the Manufacturing Engineer - (Biotech) role?
Nesco Resource is hiring for the Manufacturing Engineer - (Biotech) position, a Shazamme client. Apply directly on the employer's career site.
Where is the Manufacturing Engineer - (Biotech) job located?
The Manufacturing Engineer - (Biotech) role with Nesco Resource is based in Memphis, TN, US.
What does the Manufacturing Engineer - (Biotech) role pay?
Nesco Resource lists the Manufacturing Engineer - (Biotech) role at up to USD 43 per hour.
Is the Manufacturing Engineer - (Biotech) role full-time or contract?
This is a full time position at Nesco Resource.
What experience level is the Manufacturing Engineer - (Biotech) role?
The Manufacturing Engineer - (Biotech) position is aimed at mid-level candidates.
How do I apply for the Manufacturing Engineer - (Biotech) role at Nesco Resource?
Apply directly on Nesco Resource's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.