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Pcba Program Manager Jobs in Minnesota (NOW HIRING)

Benchmark

Sustaining Test Engineer II

Rochester, MN · On-site

$81K - $114K/yr

... PCBA). Responsibilities: • Coordinates the installation of production test equipment • Performs ... programs • Works with cross functional teams to address corrective actions • Assists ...

Benchmark

Sustaining Test Engineer I

Rochester, MN · On-site

$70K - $80K/yr

... PCBA) . Responsibilities: • Coordinates the installation of production test equipment • ... programs • Works with cross functional teams to address corrective actions • Assists ...

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Pcba Program Manager information

What is a PCBA Program Manager?

A PCBA Program Manager is responsible for overseeing the planning, execution, and delivery of projects related to Printed Circuit Board Assembly (PCBA). They coordinate cross-functional teams, manage timelines, and ensure quality and cost targets are met throughout the product lifecycle. PCBA Program Managers often serve as the main point of contact between clients, engineering, manufacturing, and supply chain teams to ensure successful project outcomes. Their role is critical in industries such as electronics, automotive, and consumer devices where efficient and reliable PCB assemblies are essential.

What are the key skills and qualifications needed to thrive as a PCBA Program Manager?

To thrive as a PCBA Program Manager, you need expertise in electronics manufacturing, program management, and a solid understanding of PCB assembly processes, typically supported by a relevant engineering degree. Familiarity with tools like ERP systems, project management software (e.g., MS Project), and industry certifications such as PMP are highly beneficial. Outstanding organizational skills, strong communication, and the ability to coordinate cross-functional teams set top performers apart in this role. These competencies are crucial for ensuring that complex PCBA projects are delivered on time, within budget, and meet quality standards.

What are some common challenges faced by a PCBA Program Manager during the product development lifecycle?

As a PCBA Program Manager, you often navigate challenges such as coordinating cross-functional teams, managing tight deadlines, and ensuring quality standards are met throughout the design, manufacturing, and testing phases. Balancing cost, quality, and time while aligning stakeholders—including engineering, procurement, and manufacturing partners—can be complex. Effective communication and proactive risk management are critical for overcoming these hurdles and ensuring successful project delivery.

What is the difference between Pcba Program Manager vs Pcba Engineer?

AspectPcba Program ManagerPcba Engineer
CredentialsBachelor's in Engineering, PMP certification often preferredBachelor's or higher in Electrical or Electronics Engineering
Work EnvironmentProject management, cross-functional teams, client interactionDesign, testing, and troubleshooting of PCBA hardware
Industry UsageUsed in manufacturing, product development, and project oversightUsed in design, development, and testing of PCBA products

The Pcba Program Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery, while the Pcba Engineer is primarily involved in designing, testing, and developing PCBA hardware. Both roles require technical knowledge, but their responsibilities differ in scope and focus.

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Pcba Program Manager jobs near you

Supplier Quality Engineer, Senior

Saint Paul, MN • On-site

Forj Medical
See more jobs at Forj Medicalexternal

$100K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 18 days ago

Key responsibilities

  • Oversee the quality of the supply base to ensure defect-free materials and services for medical devices.

  • Lead issue investigation and resolution with direct material suppliers.

  • Support supplier management activities including selection, approval, qualification, and problem resolution.

Job description

Exceptional People. Hard Problems. Meaningful Careers. Big Impact.
Nowhere else can you touch as many life-changing medical technologies. At Forj Medical, we work side by side with more than 100 medical device companies from startups to global giants to bring life-enhancing technologies to market. Working with us means solving hard problems with extraordinary people in a collaborative work environment. Join us.
Job Summary:
The Senior Supplier Quality Engineer (SQE) will oversee the quality of the Forj Medical supply base in order to ensure Forj Medical suppliers provide defect-free materials and services for complex electronic and software based medical devices. The SQE will provide technical leadership to drive continuous design and process improvements to meet quality, performance, and schedule goals. As a member of the SQE team duties include the selection and development of suppliers as well as; conducting site audits, perform source inspection, process reviews, address and resolve supplier quality related issues.
Essential Duties and Responsibilities:
    • Lead issue investigation and issue resolution with direct material suppliers.
    • Lead the activities and manage the effectiveness of business processes (i.e. NMR, Complaint Investigations, CAPA, SCARS, Process Qualification & Validation, Process Control & Monitoring, Engineering Change Control, etc...) directly supporting the production business.
    • Support the supplier management process including selection, approval/qualification and problem resolution to ensure materials delivered meet specifications.
    • Support the Quality System audit program, including leading audits as required.
    • Partner with strategic suppliers to develop capabilities and controls necessary to improve cost of quality, reduce production down time, and build predictability in material lead times.
    • Support change efforts and continuous improvement initiatives inside the company associated with Supplier Quality Engineering processes
    • Develop and mature procedures and associated processes for Supplier Quality Engineering
    • Defines/support quality performance metrics for key processes/commodities and takes appropriate action based upon resulting performance.
    • Travel approximately 10%

Required Qualifications:
    • Bachelor's degree in engineering discipline
    • Minimum 6 years' experience to include:
    • Minimum 4 years supplier quality, component engineering, and/or supplier engineering support experience.
    • Minimum 3 years' experience in FDA regulated medical device industry.
    • Demonstrated experience in processes, equipment, and control methodologies for Printed Circuit Board Assemblies (PCBA) and Printed Circuit Boards
    • Demonstrated experience in process qualification and validation for medical devices.
    • Demonstrated experience in materials qualification and validation.
    • Demonstrated experience in lean manufacturing practices and team facilitation.
    • Demonstrated experience in problem solving and root cause analysis methods.
    • Demonstrated experience in process risk management methods.
    • High proficiency in use of standard electronic business tools: Outlook, Word, PowerPoint, Excel and ERP/MRP systems.
    • Experience in use of statistical analysis software.
    • Effective communication skills of technical issues to various functional levels, ability to make data driven decisions, passionate for change and continuous improvement, and embodying a strong sense of urgency.
    • Lead Quality Auditor training/certification (ISO 13485 and/or FDA QSR)

Preferred Qualifications:
    • Experience in processes, equipment, and control methodologies for the following commodity industries:
    • Stamping and Machining
    • Injection Molding
    • Displays and Overlays
    • Experience in developing control plans during design transfer phases of projects.
    • Experience in partnering with Sourcing and Materials professionals
    • Experience Lean Six Sigma certified Green/Black belt
    • Experience in Electronics Manufacturing Services (EMS) business
    • Experience in poka-yoke strategies
    • Demonstrated leadership behaviors including effective communication at various functional levels, critical thinking and decision making, change agent, and embodying a strong sense of urgency.

Compensation
  • The expected starting salary for this position is $100,000 to $130,000 depending on qualifications. As part of your overall rewards, we offer a comprehensive benefits program.

EEO Statement
Forj Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Employment Requirement
Must be authorized to work in the United States.
Compensation and Total Rewards Package
The salary range for this position is outlined below under "Job Details" and is dependent upon the individual's skills, experience, qualifications, and applicable employment laws. Beyond base salary, Forj offers a competitive Total Rewards Package. We offer health, dental, vision, 401K plans, and time off programs. You may also be eligible to participate in an annual bonus program which depends on various factors, including, individual and organizational performance.

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