Process Engineer II, Medical device

TekWissen ®; Gary (IN); On-site; USD 46,590 - 63,383; Part time

Job summary

A global workforce management provider is seeking a Process Engineer II to support manufacturing process improvements for medical devices. The successful candidate will work on-site in Gary, Indiana, and require a Bachelor’s degree in Engineering or Technology, along with 2-4 years of experience. Responsibilities include improving manufacturing systems, supporting project timelines, and conducting technical analyses. This is a temporary assignment with a competitive pay rate ranging from $33.82 to $46.01 per hour.

Qualifications

• Bachelor’s degree from an accredited college or university.
• 2-4 years’ experience in a relevant position.
• Ability to independently make decisions impacting project objectives.

Responsibilities

• Support manufacturing process improvements under engineering guidance.
• Complete intermediate projects with supervision.
• Conduct independent analysis and develop problem-solving strategies.

Skills

Automation understanding

Six-Sigma Methodology

Knowledge of Medical Device Industry

Proficiency in SolidWorks

Technical writing competency

Education

Bachelor’s degree in Engineering or Technology

Tools

SolidWorks

Job description

Position: Process Engineer II, Medical device - Shift 1

Location: Gary, IN 46406

Duration: 6 Months

Job Type: Temporary Assignment

Work Type: Onsite

Shift: Monday – Friday 8:00 AM - 4:30 PM

Pay rate: $33.82 - 46.01/hr.

Overview:

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a, passionate about improving and saving the lives of patients through high quality, innovative medical devices and services. A leading global manufacturer of specialty medical devices that provides innovative and lifesaving solutions for the world’s healthcare markets. Specializing in Infusion Therapy, Vascular Access, Vital Care, and Specialty Products & Services.

Position Summary

The Engineer II, Manufacturing is responsible for supporting manufacturing process improvements through adherence to established design control processes, good engineering and documentation practices. The key responsibility of this position is to support and sustain production. The Engineer II will complete intermediate projects with guidance from more experienced engineers and managers. They gain exposure to some of the complex tasks within the job function and are occasionally directed in several aspects of the work.

• Under the guidance of the Engineering leadership, work to improve performance of manufacturing systems, e.g. OEE improvement (quality, performance and uptime), maintenance needs, MUV and scrap reduction
• Support project timelines and milestones and bring them to completion on time and within budget
• Assist in completion of CAPA tasks and deliverables (Corrective and Preventive)
• Use methodical approach for root cause analysis and propose robust technical solutions
• Process technical expert for a manufacturing production line
• Create and edit documents to support Production
• Support initiatives for continuous process and product improvements
• Conducts independent analysis and develops solutions to problems.
• Develops approaches and designs where precedent usually exists.
• Performs developmental and/or test work that relies heavily on a comprehensive knowledge of theory and design
• Receives general project direction. Solicits input from more experienced engineers.
• Work on special projects as they arise

Long term expectations:

• Initiate and manage projects with adherence to program-management guidelines
• Develop and characterize processes and summarize technical details
• Work with Quality Engineers on qualification activities for new or modified processes and equipment.
• Assists in training new/current employees with respect to documentation, use of equipment, laboratory techniques and department procedures.
• Delivers communications tailored to the needs of the receiver (managers, peers, customers) with appropriate frequency to maximize its utility and promote cross- functional collaboration.

Knowledge & Skills

• General understanding of automation, plastic injection molding, part assembly, fixturing, testing, and process control techniques
• Six-Sigma Methodology (DOE, Process Capability, Gage R&R, etc.)
• Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations - preferred
• Proficiency in SolidWorks. Mechanical understanding, tool design experience
• Technical writing competency
• Competent in your domain.
• Familiar with other areas of domain expertise within the team.
• Has a basic understanding of best practices.
• Has a basic to intermediate understanding of engineering discipline
• Have awareness of the broader product strategy and contribute to it
• Ability to receive general project direction and solicit input from more experienced engineers.
• Requires the ability to independently make decisions that impact the attainment of project objectives.

Minimum Qualifications, Education & Experience

• Must be at least 18 years of age
• Bachelor’s degree from an accredited college or university (Engineering, Technology,
• 2-4 years’ experience
• This job operates in a professional office environment and routinely uses standard office equipment
• Work is performed in a clean room environment.
• While performing the duties of this job, the employee is regularly required to work with contaminated Medical Devices in a controlled laboratory setting
• Must be able to occasionally move objects up to 15 lbs.

TekWissen® Group is an equal opportunity employer supporting workforce diversity.