Senior Engineer
Talent Software Services, Inc.
Job Description
Job Description
Job Details
Job Title: Senior Engineer
Location: Irvine, California
Duration: 6 months
Experience Required: 6–8 years
Essential Skills:
Medical Device Industry and Regulations
New Product Development (NPD) Methodology and Management
Skill Category: EIS – Medical Device & Regulations / NPD Methodology and Management
Knowledge and experience in Product Development and New Product Development (NPD).
Ability to design and develop electromechanical systems and components.
Experience integrating mechanical and electrical components into complete systems.
Knowledge of stepper motors, motor drivers, sensors, and PLC programming for equipment design.
Experience performing mechanical, electromechanical, and developmental design activities with limited supervision.
Experience in industrial automation, robotics, or precision instruments is preferred.
Strong experience with SolidWorks and CAD software.
Knowledge of Geometric Dimensioning and Tolerancing (GD&T).
Knowledge of Good Manufacturing Practices (GMP) and manufacturing documentation, preferably in the medical device industry.
Knowledge of ISO 13485 and medical device regulatory standards, including MDD and MDR.
Knowledge of Statistical Analysis and Design of Experiments (DOE) is preferred.
Proficiency in computer applications and engineering software.
Strong interpersonal, communication, organizational, planning, and project management skills.
Proficiency in Microsoft Office applications, including:
Microsoft Word
Microsoft Excel
Microsoft PowerPoint
Microsoft Project
Email and web browsers
Project planning and spreadsheet software
Identify, design, and develop equipment required for new product development.
Study existing manufacturing processes and implement improvements to support new products.
Implement automation solutions in manufacturing processes and tooling.
Prepare, manage, and maintain engineering specifications.
Assist technicians and engineers in troubleshooting and resolving unusual technical problems.
Purchase and design equipment that meets applicable safety and environmental requirements.
Perform process and product validation activities.
Supervise, coordinate, and technically review the work of a limited group of technicians.
Communicate business-related issues, project updates, and improvement opportunities to the next level of management.
Ensure engineering activities comply with applicable federal, state, and local regulations, corporate procedures, and guidelines.
Support mechanical and electromechanical design activities under limited supervision.
Contribute to continuous process improvement and automation initiatives.
Perform other duties and responsibilities as assigned.
No specific generic managerial skills are listed.
Strong communication and interpersonal skills are expected.
Ability to collaborate effectively with engineers, technicians, and cross-functional teams.
Strong organizational, planning, and project management capabilities.
Electromechanical Engineering
New Product Development (NPD)
Mechanical Design
Product Development Processes
Industrial Automation
Mechatronics
Fixture Design
SolidWorks
CAD Software
Geometric Dimensioning and Tolerancing (GD&T)
PLC Programming
Stepper Motors, Motor Drivers, and Sensors
Process and Product Validation
Design of Experiments (DOE)
Medical Device Regulations
ISO 13485, MDD, MDR, and GMP
Overall experience: 6–8 years.
Medical device industry experience: Minimum 5 years; 5–8 years preferred.
NPD experience: Knowledge and experience in New Product Development are required.
Automation experience: Knowledge of automation is mandatory for screening.
Design experience: Hands-on experience in mechanical and electromechanical design, CAD, and SolidWorks.
Regulatory knowledge: Familiarity with medical device quality systems and regulatory requirements.
Electromechanical Engineering
Product Development Processes
Fixture Design
Mechanical Design
CAD
SolidWorks
Design of Experiments (DOE)
New Product Development (NPD)
Mechatronics
Industrial Automation
PLC Programming
Medical Devices
GD&T
Process Validation
- 1. Medical Device Industry Experience: How many years of experience does the candidate have in the medical device domain?
Minimum requirement: 5 years.
Preferred experience: 5–8 years.
- 2. NPD and Automation Knowledge: Does the candidate have knowledge and experience in New Product Development (NPD) and automation?
If No: Reject the candidate.
- 3. Relocation: Is the candidate willing to relocate to Irvine, California?
If No: Reject the candidate.
$165k - $175k
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