Job Description

Title: Process Engineer Associate

Location: Tucson, AZ 85755

Duration: 2 years with possible extension

Pay Range: $27-35 per hour

About Client:

Specializing in advanced digital pathology solutions, this company revolutionizes the way medical professionals analyze and interpret tissue samples. Focusing on high-resolution imaging and cutting-edge software, it provides tools that enhance diagnostic accuracy and streamline workflow. Its innovative technologies are pivotal in improving patient outcomes and advancing research in various fields of medicine.

Overview:

Participates in and leads validations and projects within the manufacturing areas. This engineer is responsible for successful project completion including necessary reports and approvals. Identifies and assists with implementing improvements around current manufacturing processes with guidance from the manager and senior engineers. Responsibilities also include equipment, process validations, process characterization, and root cause investigations.

Responsibilities:

• Evaluate existing assembly processes and identify areas for improvement.
• Work to implement new manufacturing processes promptly.
• Update, create, and sustain Standard Work documents.
• Create and update drawings using Pro/Engineer or SolidWorks.
• Work as part of a project team in developing and implementing automated processes.
• Lead and/or participate in equipment and process validations.
• Provide technical support for daily production issues related to manufacturing equipment.
• Strong written and verbal communication skills.
• With guidance, able to prepare and present technical information and project summaries to peers and management.
• Monitors work to ensure quality and to continuously promote Quality First Time.

Education:

• Bachelor's Degree BS degree or equivalent in a directly related discipline

Experience:

• Years of Experience Details
• Less than 1 year or 2 years related experience preferred

Knowledge, Skills, and Abilities:

• Experience with automated manufacturing equipment and automation technologies
• Knowledge of FDA Quality System Regulations (QSRs) is a plus
• Experience with CAD programs such as Pro/Engineer and/or SolidWorks
• Strong computing skills utilizing Microsoft Office tools such as Excel, Word, and PowerPoint
• Strong teamwork skills
• Skilled in troubleshooting and problem-solving
• Ability to meet project deadlines
• Ability to multitask and prioritize with guidance from management

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