Manufacturing Engineering Manager

Posted 3 Days Ago
Be an Early Applicant
Maple Grove, MN, USA
In-Office
Senior level
Healthtech
The Role
Leads manufacturing engineering for medical device commercial production, including new product introduction, process transfer, validation, automation, equipment qualification, tooling, sustaining engineering, and continuous improvement. Supervises engineering staff, manages KPIs and capital projects, supports troubleshooting and CAPA investigations, and ensures compliance with 21 CFR Part 820, ISO 13485, GDP, EHS policies, and customer requirements.
Summary Generated by Built In

The Manufacturing Engineering Manager leads the manufacturing engineering team supporting new product introduction and transfer, process development and validation, automation, and sustaining engineering at Nextern’s US medical device CDMO site, delivering capable, compliant, and cost-effective manufacturing processes in support of commercial production at the Maple Grove facility.


Requirements

DUTIES AND RESPONSIBILITIES:

· Lead daily manufacturing engineering activities, including process development, equipment and tooling support, automation, and sustaining engineering for commercial production lines.

· Supervise, train, and develop manufacturing and process engineers and engineering technicians; set objectives and manage performance.

· Establish and track KPIs (first pass yield, scrap and rework, OEE, cycle time, on-time completion of engineering deliverables) and drive corrective actions.

· Partner with operations, quality, program management, and customers to support commercial production schedules and product transfer milestones.

· New Product Introduction & Transfer

Lead transfer of customer designs into commercial production, including process development, tooling and fixturing, line layout, and capacity planning.

· Own process characterization and validation (IQ/OQ/PQ), test method validation, and pFMEA and control plan development.

· Provide design for manufacturability (DFM) feedback to customers and internal design teams during development.

· Process & Equipment Engineering

· Specify, qualify, and maintain manufacturing equipment, automation, tooling, and fixtures; manage capital projects from justification through installation and qualification.

Drive process capability improvements using statistical methods (SPC, Cp/Ppk, DOE) to reduce variation, scrap, and rework.

· Provide technical troubleshooting for production issues, nonconformances, and CAPA investigations; implement effective root cause corrective actions.

· Compliance & Continuous Improvement

· Ensure processes, validations, and records comply with 21 CFR Part 820, ISO 13485, GDP, and site EHS/safety policies; support internal, customer, and regulatory audits.

· Apply lean, 5S, and Six Sigma principles to improve manufacturing flow, reduce cost, and increase throughput and capacity.

SUPERVISORY RESPONSIBILITIES:

· Directly supervises manufacturing engineering staff, including manufacturing and process engineers, automation engineers, and engineering technicians. Responsibilities include hiring, training, scheduling, performance management, and development in accordance with company policies and applicable laws.

QUALIFICATIONS:

· Bachelor's degree in mechanical, manufacturing, biomedical, or industrial engineering, or a related technical field required; advanced degree a plus.

· 8+ years of progressive manufacturing or process engineering experience, including 2+ years in a leadership role; medical device or regulated manufacturing strongly preferred.

· Demonstrated experience transferring new products into commercial production, including process development, process validation (IQ/OQ/PQ), and test method validation.

· Hands-on experience with automation, tooling and fixture design, and equipment qualification; CAD proficiency (SolidWorks or equivalent).

· Certifications preferred: Six Sigma Green Belt or Black Belt, Lean, or PMP.

· Working knowledge of 21 CFR Part 820, ISO 13485, and Good Documentation Practices; experience with design controls, risk management (ISO 14971), pFMEA, and CAPA.

· Strong statistical, problem-solving, and communication skills; proficiency with Minitab or equivalent and data-driven decision making.

· Perform other related duties as assigned by management.


Benefits
  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan with Company Match
  • Paid Time Off, Personal Days, AND Birthday Holiday!
  • Lifetime Membership Subsidy and Wellness Resources
  • Life Insurance (Basic, Voluntary & AD&D)
  • Family Leave (Maternity, Paternity)
  • Short-Term & Long-Term Disability
  • Taco Thursdays!!!

Nextern is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences, and we are committed to fostering an inclusive and diverse workplace. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Skills Required

  • Bachelor's degree in mechanical, manufacturing, biomedical, industrial engineering, or a related technical field
  • 8+ years of progressive manufacturing or process engineering experience
  • At least 2 years of experience in a leadership role
  • Experience transferring new products into commercial production
  • Experience with process development, IQ/OQ/PQ process validation, and test method validation
  • Hands-on experience with automation, tooling and fixture design, and equipment qualification
  • CAD proficiency with SolidWorks or equivalent
  • Working knowledge of 21 CFR Part 820, ISO 13485, and Good Documentation Practices
  • Experience with design controls, ISO 14971 risk management, pFMEA, and CAPA
  • Strong statistical, problem-solving, and communication skills
  • Proficiency with Minitab or equivalent
  • Medical device or regulated manufacturing experience
  • Advanced degree
  • Six Sigma Green Belt or Black Belt certification
  • Lean certification
  • PMP certification
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Saint Paul, MN
172 Employees
Year Founded: 2000

What We Do

Nextern collaborates with innovators, clinicians, and device partners to create, iterate, optimize and manufacture best-in-class medical devices. We bring an unmatched core competence in medical device product design and development through manufacturing as a leverageable asset to collaborators like you, who are focused on accelerating the commercial side of the business.​

Similar Jobs

The Aerospace Corporation Logo The Aerospace Corporation

Engineering Manager

Aerospace • Artificial Intelligence • Cloud • Machine Learning • Software • Cybersecurity • Defense
Hybrid
Plymouth, MN, USA
4600 Employees

Northrop Grumman Logo Northrop Grumman

Manager Manufacturing Engineering 1

Aerospace • Logistics • Security • Software • Cybersecurity
In-Office
Plymouth, MN, USA
85636 Employees
105K-158K Annually

nVent Logo nVent

Sr Manager, Manufacturing Engineering

Hardware • Information Technology • Energy • Design • Utilities • Industrial • Renewable Energy
In-Office
Anoka, MN, USA
10001 Employees
124K-230K Annually

The Toro Company Logo The Toro Company

Engineering Manager

Greentech • Other • Real Estate
In-Office
Windom, MN, USA
10001 Employees
120K-140K Annually

Similar Companies Hiring

Sailor Health Thumbnail
Healthtech • Social Impact • Telehealth
New York City, NY
20 Employees
Granted Thumbnail
Artificial Intelligence • Healthtech • Insurance • Mobile • Financial Services
New York, New York
23 Employees
OneImaging Thumbnail
Healthtech
Miami, FL
62 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account