COMPANY DESCRIPTION

SunMed is a respected North American manufacturer and distributor of one of the most comprehensive portfolios of consumable medical devices for anesthesia and respiratory care. For more than 40 years, SunMed has expanded their product offering by adding reputable brands such as Salter Labs, Ventlab, Ethox Medical, and Westmed. The SunMed family of brands offers a product portfolio that spans the continuum of care from first responder to home care, with safety, patient comfort, and clinical performance in mind.

POSITION SUMMARY

POSITION QUALIFICATIONS

• The ideal candidate for this position will have knowledge of the design and development processes used for medical devices and a background in project management.
• Experience with manufacturing processes for plastic components such as injection molding knowledge is preferable.

• The candidate will have the ability to work with mathematical concepts and apply those concepts to practical situations; proficiency with standard computer software.
• Proficiency in project management tools such as MS Project is required.
• Knowledge of CAD software, specifically Solidworks, is highly desired.
• Exceptional communication skills required.

LEVEL OF EXPERIENCE

• 7 + years of experience in an engineering and/or project management position.
• Experience in a medical device, pharmaceutical, or plastics manufacturing facility is a plus.

LEVEL OF EDUCATION

• The position requires the candidate to at least have a Bachelor’s Degree in manufacturing, industrial, mechanical, or related engineering.

• The amount of time required for this position will depend on specific project requirements.

ESSENTIAL DUTIES AND RESPONSIBILITIES

• 
  Successful planning and execution of complex projects using internal and external resources across a global manufacturing organization.
• Lead multiple large-scale projects at one time, ensuring schedules and deliverable expectations are met.
• Identify, scope, and present potential cost savings and efficiency opportunities to a cross-departmental review board.
• Oversee product improvement projects and manage project timelines.
• Manage projects including resource allocation.
• Become the subject matter expert related to specific products, manufacturing processes, and internal processes.
• Write, review, modify, and approve Process and Product validation documents per FDA guidelines.
• Create and modify existing product specifications based on global standards (ISO), and customer requirements.
• Train associates with work techniques, and skills required to perform product assembly or processing.

• Assist in maintaining Food & Drug Administration (FDA), Good Manufacturing Practices (GMP), and ISO Compliance.

OTHER RESPONSIBILITIES

• Focus on achieving our Company mission
• Demonstrate accuracy and thoroughness in daily work; look for ways to improve and promote quality & safety.
• Inspire the trust of others; treat people with respect and dignity, and embrace the value of diversity.
• Use time efficiently; perform job accurately, thoroughly, and conserve Company resources to improve profits.
• Contribute to building and maintaining a positive team environment.

• Assure all policies and guidelines are implemented and followed.

QUALITY POLICY

At SunMed, Quality is our promise. It is our commitment to customer satisfaction and our dedication to product excellence in an evolving global healthcare market. This promise is kept through a continuously improving and effective Quality Management System and compliance to Regulatory Requirements.

DEIA STATEMENT

At SunMed, we are committed to building a diverse workforce and an inclusive workplace that reflects the communities and customers we serve.

We believe our philosophy on Diversity, Equity, Inclusion, and Advancement (DEIA) encourages excellence and equips us to serve an evolving global marketplace.