Please Contact:

To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Priyanka Mahant at email address Priyanka.mahant can be reached on # . We have Contract role Development Process Engineer f or client at St. Paul, MN. Please let me know if you or any of your friends would be interested in this position.

Position Details:

Development Process Engineer- St.

Paul, MN Location :

St. Paul, MN 55117 (On-site)

Project Duration:

07+ Months of contract

Shift :

8:00 AM - 5:00 PM (Mon-Fri)

Pay Rate :

$31.00 per hour on W2

Key Responsibilities:

Process Development & Implementation:

Lead the design, development, and implementation of new manufacturing processes and equipment. Specify, acquire, and validate new equipment to support production and process improvements.

Problem Solving & Root Cause Analysis:

Apply structured problem-solving methodologies to identify root causes of process issues. Develop and implement corrective and preventive actions (CAPAs).

Data-Driven Improvements:

Design and execute experiments (DOE), analyze data, and present findings to cross-functional teams. Drive continuous improvement initiatives to enhance product quality, reduce waste, and increase efficiency.

Documentation & Compliance:

Create and maintain technical documentation including SOPs, risk assessments, validation protocols, and safety instructions. Ensure all processes comply with internal quality systems and external regulatory requirements.

Cross-Functional Collaboration:

Work closely with R D, Quality, Manufacturing, and Supply Chain teams to support product development and scale-up. Provide technical training and mentorship to technicians and junior engineers.

Innovation & Technical Leadership:

Evaluate and recommend new materials, tools, and technologies to improve manufacturing capabilities. Support tooling development and process validation for new and existing products.

Required Qualifications:

Bachelor s degree in engineering (Mechanical, Biomedical, Chemical, or related field) with 2 5+ years of relevant experience OR master s degree with 0 2 years of experience or an equivalent combination of education and experience. Strong analytical and problem-solving skills. Proficiency in technical writing and documentation. Ability to work independently and collaboratively in cross-functional teams. Excellent communication and presentation skills. Working knowledge of manufacturing systems, automation, and process control.

Preferred Qualifications:

Experience in the medical device industry, particularly with catheter manufacturing or similar regulated environments. Familiarity with

GMP, ISO

13485, and FDA regulations. Hands-on experience with process validation, DOE, and statistical analysis. To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Priyanka Mahant at email address Priyanka.mahant can be reached on # .