Entry Level Biomedical/Mechanical Engineer- 2nd shift

Job Summary:

We are seeking a Quality Engineer to support manufacturing and quality operations within a medical device environment. This role will focus on identifying manufacturing process issues, supporting root cause investigations, improving product quality, and partnering with cross-functional teams to ensure compliance with quality standards. This is an excellent opportunity for candidates with medical device manufacturing experience or recent Master's graduates in Mechanical Engineering or Bioengineering looking to build their careers in quality engineering.

Key Responsibilities:

• Support manufacturing quality activities by reviewing and dispositioning nonconforming materials

• Assist with root cause investigations, corrective actions, and preventive action activities

• Support process monitoring and quality improvement initiatives to reduce variation and improve product performance

• Review product specifications, quality documentation, and manufacturing procedures to ensure compliance

• Participate in risk assessments, failure analysis, and process improvement projects

• Analyze quality metrics and support continuous improvement activities

• Collaborate with manufacturing, engineering, and quality teams to resolve product and process issues

• Support product release activities and documentation requirements

• Maintain compliance with quality system procedures and regulatory requirements

• Contribute to sustaining engineering and new product development quality initiatives

Required Qualifications:

• Bachelor’s degree in Mechanical Engineering, Bioengineering, Biomedical Engineering, Manufacturing Engineering, Quality Engineering, or a related technical discipline

• One to five years of experience in a manufacturing, quality, or engineering environment

• Basic understanding of quality engineering principles and manufacturing processes

• Knowledge of root cause analysis and continuous improvement methodologies

• Strong analytical, problem-solving, and documentation skills

• Ability to work effectively in a cross-functional team environment

• Familiarity with regulated manufacturing environments

Preferred Qualifications:

• Master’s degree in Mechanical Engineering, Bioengineering, Biomedical Engineering, or related field

• Experience in medical device manufacturing

• Exposure to risk analysis, FMEA, CAPA, or nonconformance management

• Knowledge of quality systems and regulatory requirements

• Internship, co-op, or research experience within medical device or healthcare manufacturing environments

Benefits:

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

Pay Range: $30/hr to $38.hr