Quality Engineer (Non-Light Industrial)

Integrated Resources Inc.; Franklin Lakes (NJ); On-site; USD 80,000 - 110,000; Full time

Job summary

A reputable staffing firm is seeking a Quality Engineer in Franklin Lakes, NJ, specializing in the Medical Device/Biotechnology Industry. The role includes ensuring product quality compliance, guiding cross-functional teams, and maintaining design history files. Candidates must have a relevant BS degree and industry experience.

Qualifications

• Minimum of 4-5 years of experience in the Medical Device/Biotechnology Industry.
• Professional certifications preferred.

Responsibilities

• Ensure product and process quality compliance.
• Coordinate cross-functional teams to meet quality objectives.
• Develop and maintain design history files.

Skills

Regulatory requirements

Risk management

Product development

Education

BS degree in Electrical Engineering

BS degree in Software/Computer Science

Professional certifications (CQA, CQE, SQE, CQM)

Job description

A Few Words About Us

Integrated Resources, Inc. is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Hi [[CandidateFirstName]],

I came across your resume online and found it very impressive. I have an immediate opening with one of my direct clients.

Below are the position details. Please let me know if you are available/interested so we can discuss this opportunity further.

Job Title: Quality Engineer (Non-Light Industrial)

Location: Franklin Lakes, NJ

Duration: 6+ months (possibility of extension)

Qualifications:

• BS degree in Electrical Engineering, Software/Computer Science, or a similar discipline, with a minimum of 4-5 years of experience in the Medical Device/Biotechnology Industry.
• Professional certifications such as CQA, CQE, SQE, CQM are preferred.

Responsibilities:

• Work closely with Manufacturing, R&D, Quality, Engineering, Procurement, and Marketing to ensure product and process quality compliance.
• Coordinate and guide cross-functional teams to meet software quality objectives for product, manufacturing, and quality system software.
• Demonstrate expertise in product development, software lifecycle, regulatory requirements, standards, and risk management.
• Develop and maintain design history files.

Feel free to share this job opportunity with friends or colleagues who might be interested.

Thanks & Regards,

Seema Chawhan

Clinical Recruiter

Integrated Resources, Inc.

Direct: 732-318-6506 | Work: 732-549-2030 Ext 324 | Fax: [phone]

Email: [e-mail] | www.irionline.com

LinkedIn: https://in.linkedin.com/in/seemachawhan

Gold Seal JCAHO Certified for Health Care Staffing

"INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)

Additional Information

Thanks & Regards,

Seema Chawhan

Clinical Recruiter

Integrated Resources, Inc.

Direct: 732-318-6506 | Work: 732-549-2030 Ext 324 | Fax: [phone]

Email: [e-mail] | www.irionline.com

LinkedIn: https://in.linkedin.com/in/seemachawhan

Gold Seal JCAHO Certified for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)