Senior Manufacturing Engineering Technician

Job Description

Job Description

Job Title: Experienced Manufacturing Engineering Technician

Job Description

The Manufacturing Engineering Technician supports daily manufacturing operations, process development, and qualification activities for production tissue heart valves at a fast-paced startup environment in Plymouth, MN. This role focuses on regulated medical device manufacturing and involves close collaboration with cross-functional manufacturing and engineering teams to ensure reliable, efficient, and compliant production processes.

Responsibilities

• Provide daily technical support for operations in the metals, valve assembly, and packaging areas to ensure smooth and efficient production.
• Identify, investigate, and implement corrective actions for manufacturing-related issues to improve product quality and process reliability.
• Perform equipment setup and execute corrective, preventive, and calibration maintenance as needed to maintain optimal equipment performance.
• Install and validate manufacturing equipment and processes in accordance with required validation requirements and regulatory standards.
• Develop tooling and fixtures to support new and existing manufacturing processes and improve production efficiency.
• Plan, order, and coordinate the procurement of equipment, tools, and fixtures to support manufacturing operations and process improvements.
• Manage and maintain manufacturing equipment, including troubleshooting issues, performing preventive maintenance activities, and supporting asset management.
• Support floor-level material and tool organization using Kanban replenishment systems to maintain efficient and orderly production areas.
• Participate in process development projects by working closely with engineering teams on process improvements and optimization initiatives.
• Collaborate with engineering on projects and continuous improvement ideas to enhance manufacturing processes and product quality.
• Adhere to and support general safety rules, manufacturing procedures, company policies and procedures, and applicable regulations.
• Ensure compliance with Quality System Regulation (QSR) and ISO standards in all manufacturing and validation activities.

Essential Skills

• 5+ years of experience in regulated manufacturing environments, preferably within the medical device industry.
• Strong experience in medical device manufacturing, including familiarity with regulated production environments and quality systems.
• Hands-on experience with equipment validation, including installation, operational, and performance qualification activities.
• Demonstrated troubleshooting skills for manufacturing processes and equipment issues.
• Experience with continuous improvement and process improvement initiatives in a manufacturing setting.
• Knowledge of lean manufacturing principles and their application on the production floor.
• Experience in manufacturing engineering or process engineering roles supporting production operations.
• Ability to perform equipment setup, corrective maintenance, preventive maintenance, and calibration maintenance.
• Understanding of QSR and ISO standards and their application in a regulated manufacturing environment.
• Ability to work effectively in a fast-paced startup environment and collaborate with cross-functional teams.

Additional Skills & Qualifications

• Experience with manufacturing processes for metals, valve assembly, and packaging operations.
• Past in manufacturing process development and optimization.
• Experience with tooling and fixture development to support new and existing processes.
• Familiarity with Kanban systems for material and tool organization on the manufacturing floor.
• Experience planning and ordering equipment, tools, and fixtures to support production and engineering projects.
• Demonstrated ability to support maintenance and equipment management, including asset management activities.
• Strong communication skills to collaborate effectively with manufacturing and engineering teams.
• Comfort working as a technician with responsibility for supporting production and process improvement activities.

Work Environment

This role is primarily based on the manufacturing floor with limited desk time, providing a hands-on environment focused on production tissue heart valves in a regulated medical device setting. The position operates on a first shift schedule, Monday through Friday, from 7:00 a.m. to 3:30 p.m. You will work closely with cross-functional manufacturing and engineering teams in a fast-paced startup atmosphere that emphasizes collaboration, continuous improvement, and adherence to safety, QSR, and ISO standards. The environment involves regular interaction with production equipment, tools, fixtures, and Kanban-based material organization systems.

This is a Contract to Hire position based out of Plymouth, MN.

The pay range for this position is $30.00 - $38.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Plymouth,MN.

This position is anticipated to close on Aug 28, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.