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Job Description HumCap's client, a company in the biomedical technology space, is searching for a Manufacturing Engineer to join their team.
Plans, designs and analyzes manufacturing processes for devices and drug products.
Owns technical aspects of new‑product‑introduction activities to transfer designs robustly into manufacturing.
Determines equipment, tools, and processes needed to achieve manufacturing goals according to product specifications.
Maximizes efficiency by optimization of layout of equipment, workflow, assembly methods, and workforce utilization.
RESPONSIBILITIES
Develop detailed layouts for equipment, manufacturing processes, and workflow.
Evaluate existing manufacturing processes to identify areas for improvements.
Research and develop new and/or improved processes, equipment, and products.
Design, purchase, install, characterize, and validate manufacturing equipment, fixtures, specialty assembly tools.
Develop, author, execute and document engineering investigations, process development studies, manufacturing work instructions, risk assessments, and validation protocols/reports (IQ, OQ, PQ).
Process owner for nonconformances and CAPAs that arise from manufacturing issues.
Own interactions with contract manufacturers and component suppliers for issue resolution, component qualification, cost reduction and quality improvements.
Partner with Research to evaluate designs for manufacturability prior to production.
Implement graphic arts designs and controlled content on finished product labels and packaging.
QUALIFICATIONS Experience and Education
Experience: Bachelor’s degree in engineering, preferably Mechanical Engineering, Electrical Engineering, Biomedical Engineering or related field required.
Minimum 5 years’ experience in medical devices, including a minimum of 3 years supporting active manufacturing operations under strict quality‑system controls.
Experience in contract manufacturing required.
Experience with manual and semi‑automated assembly processes for electromechanical devices required.
Familiar with processes for sterilization, bioburden, and endotoxin testing.
Experienced with design transfer / new product introduction; has borne significant responsibilities in successful launch of at least one product, ideally orthopedic.
Experienced in requirements development, design‑change analysis, risk management, and change‑control procedures.
Understanding of GxP, FDA Quality System Regulations, ISO 13485, and ISO 14971.
Skills and Abilities
Excellent organizational and communication skills.
Ability to prioritize tasks and manage multiple projects effectively.
Demonstrates entrepreneurial spirit; able to thrive and contribute impactfully in an agile startup environment.
Hands‑on, driven work ethic, with high attention to detail, and high ownership approach to process/product quality.
Ability to communicate complex technical data in format appropriate to support critical decision‑making activities; excellent presentation skills and technical writing ability.
Solid grasp of statistical methods applicable to process development, investigations, and validation.
Able to engage effectively with peers and project colleagues at contract manufacturing organizations, and with suppliers.
Computer Software / Programs (Required)
Microsoft Office
Google Suite
SolidWorks or comparable CAD software
Minitab or comparable statistics software
Computer Software / Programs (Desired)
SmartSheet project management software
Python programming
Graphic‑art software (e.g., Adobe Illustrator)
Commercial label‑software (e.g., Bartender, Nicelabel, Labelview)
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr
We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
Job Description HumCap's client, a company in the biomedical technology space, is searching for a Manufacturing Engineer to join their team.
Plans, designs and analyzes manufacturing processes for devices and drug products.
Owns technical aspects of new‑product‑introduction activities to transfer designs robustly into manufacturing.
Determines equipment, tools, and processes needed to achieve manufacturing goals according to product specifications.
Maximizes efficiency by optimization of layout of equipment, workflow, assembly methods, and workforce utilization.
RESPONSIBILITIES
Develop detailed layouts for equipment, manufacturing processes, and workflow.
Evaluate existing manufacturing processes to identify areas for improvements.
Research and develop new and/or improved processes, equipment, and products.
Design, purchase, install, characterize, and validate manufacturing equipment, fixtures, specialty assembly tools.
Develop, author, execute and document engineering investigations, process development studies, manufacturing work instructions, risk assessments, and validation protocols/reports (IQ, OQ, PQ).
Process owner for nonconformances and CAPAs that arise from manufacturing issues.
Own interactions with contract manufacturers and component suppliers for issue resolution, component qualification, cost reduction and quality improvements.
Partner with Research to evaluate designs for manufacturability prior to production.
Implement graphic arts designs and controlled content on finished product labels and packaging.
QUALIFICATIONS Experience and Education
Experience: Bachelor’s degree in engineering, preferably Mechanical Engineering, Electrical Engineering, Biomedical Engineering or related field required.
Minimum 5 years’ experience in medical devices, including a minimum of 3 years supporting active manufacturing operations under strict quality‑system controls.
Experience in contract manufacturing required.
Experience with manual and semi‑automated assembly processes for electromechanical devices required.
Familiar with processes for sterilization, bioburden, and endotoxin testing.
Experienced with design transfer / new product introduction; has borne significant responsibilities in successful launch of at least one product, ideally orthopedic.
Experienced in requirements development, design‑change analysis, risk management, and change‑control procedures.
Understanding of GxP, FDA Quality System Regulations, ISO 13485, and ISO 14971.
Skills and Abilities
Excellent organizational and communication skills.
Ability to prioritize tasks and manage multiple projects effectively.
Demonstrates entrepreneurial spirit; able to thrive and contribute impactfully in an agile startup environment.
Hands‑on, driven work ethic, with high attention to detail, and high ownership approach to process/product quality.
Ability to communicate complex technical data in format appropriate to support critical decision‑making activities; excellent presentation skills and technical writing ability.
Solid grasp of statistical methods applicable to process development, investigations, and validation.
Able to engage effectively with peers and project colleagues at contract manufacturing organizations, and with suppliers.
Computer Software / Programs (Required)
Microsoft Office
Google Suite
SolidWorks or comparable CAD software
Minitab or comparable statistics software
Computer Software / Programs (Desired)
SmartSheet project management software
Python programming
Graphic‑art software (e.g., Adobe Illustrator)
Commercial label‑software (e.g., Bartender, Nicelabel, Labelview)
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr