Description
Exciting 3-month contract opportunity for a Quality Engineer in Phillipsburg, NJ! This growing medical device company is dedicated to advancing healthcare solutions through innovative design and manufacturing. With a small, tight-knit team and the backing of a larger parent organization, this is a chance to contribute to meaningful projects in a hybrid role that combines onsite collaboration with flexible remote work. If you’re looking to make an immediate impact and play a key role in documentation, project management, and compliance within the medical device industry, this is the role for you!
Qualifications and responsibilities for this Quality Engineer position include:
- Minimum of 3 years of experience in a medical device or ISO-regulated environment
- Strong knowledge of FDA 21 CFR 820, ISO 13485, ISO 14971, and MDR regulations
- Proficiency in Microsoft Office for documentation and management tasks
- Experience with quality management systems, ISO 345 certification, and EU CE compliance
- Responsible for project documentation including Quality Plans, Regulatory Plans, and Project Plans
- Ensure compliance with QSR and GMP requirements in assigned areas
- Manage documentation and process flow for new medical device development projects
- Utilize quality tools such as FMEA, control plans, and risk analysis
Salary: $30.00 - $50.00 per hour, commensurate with experience.
DAVRON is the leading Headhunter and Executive Search firm for Engineering, Architecture, Construction and Manufacturing professionals nationwide. Our recruiters have direct communication with hiring managers allowing us to get you in front of company decision makers. You also receive one-on-one interview preparation and insider coaching from staffing experts to help you every step of the way. We want to see you thrive in challenging work environments that bring you excitement and prosperity in your career!
Apply Now!
Are you ready to take the next step in your career and thrive in a challenging work environment? If so, apply today and let's see where this opportunity can take you!
QUALITY ENGINEER | QUALITY ASSURANCE ENGINEER | QUALITY MANAGEMENT | FDA 21 CFR 820 | ISO 13485 | ISO 14971 | MEDICAL DEVICE DOCUMENTATION | PROJECT MANAGEMENT | MICROSOFT OFFICE | RISK MANAGEMENT | GMP COMPLIANCE | FMEA