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Supervisor, Engineering

Medivators Inc.
Posted 2 days ago, valid for a month
Location

Plymouth, MN, US

Salary

$116,238 - $136,750 per year

Contract type

Full Time

Paid Time Off
Tuition Reimbursement

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Sonic Summary

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  • The Engineering Supervisor position in Minneapolis, MN involves directing manufacturing engineers and technicians while ensuring project milestones are met.
  • Candidates must have a Bachelor's degree in a relevant engineering discipline and a minimum of 7 years of experience in a manufacturing environment.
  • The salary for this role ranges from $116,237.50 to $136,750, with eligibility for bonus participation.
  • Responsibilities include people management, collaboration with cross-functional teams, and adherence to quality standards throughout the product development process.
  • The position requires strong leadership, organizational skills, and the ability to drive continuous improvement in a regulated environment.

Position Summary

The Engineering Supervisor in our Minneapolis, MN location directs the work of manufacturing engineers and engineering technicians as well as other technical roles as described in a value stream.  The Engineering Supervisor sets engineering milestones and ensures that user needs and requirements are gathered and fully understood. This role is responsible for making sure the team has contingency plans in place to ensure setbacks do not result in manufacturing delays.  Works within a defined schedule to identify action items and engineering milestones to keep projects on track.  Responsible for the people management, functional competency development, and execution of product development activities.  The responsibilities for this position include but are not limited to directing and managing NPD or Sustaining activities. Responsible for the skills and capabilities growth of individuals on the team.  Responsible for collaboration with other development leads and engineers.  This person has engineering responsibilities in addition to the supervising responsibilities. Must adhere to systems and controls to ensure compliance with quality standards and manage the product design end-to-end.

 

The Engineering Supervisor develops strategy for manufacturing operations, including required technology and needed resources. This role is responsible for the development efforts of their team during all phases of program from inception to completion of a commercialized product including launch and post launch follow up. The recommendations from the Engineering Supervisor have a significant impact on the development path of a project. 

This role requires working within a cross-functional team supporting the development plans for a product. Must be familiar with a wide variety of the design concepts, practices, and procedures and relies on experience and good judgment to plan and accomplish goals. A wide degree of creativity and latitude is expected. Reports to and takes work direction from the Engineering Manager.

Own the success of product and/or development project(s).

  • Team leadership including staffing, roles, and responsibility definitions, and influencing other critical departments in the organization. 
  • Utilize strong organizational and milestone tracking skills.
  • Contribute and lead execution of departmental goals and objectives.
  • Establish operating mechanisms to drive collaboration, and decision-making agility.

 

This position requires working onsite in our Plymouth, MN location 7:00 am to 4:30 pm Monday through Friday, with occasional earlier or weekend hours based on business needs. 

 

What You’ll do as an Engineering Supervisor

  • Directs the work of Manufacturing Engineers and Engineering Technicians within their team. Facilitates communication and interaction among core team members to ensure transparency of critical deliverables and milestones in the NPD / Sustaining process. Ensures technical plans are developed and executed within expectations of project deliverables. 
  • Actively contributes to projects in development by completing engineering tasks and having engineering responsibilities such as documentation and design activities.
  • Contributes to continuous improvement ideas to better the department. Also works with direct reports on training and development plans. 
  • Identifies opportunities related to strategy and scope within manufacturing value streams.
  • Demonstrates a commitment to patient safety and product quality by maintaining compliance with all Quality Systems requirements. Fully adheres to all applicable FDA regulations, international guidelines, and company policies at all times. Establishes and promotes a work environment amongst co-workers and direct reports that supports compliance with the Quality System and company policy.
  • Drives culture of High-Performance teams in the department through strategic initiatives (functional competencies, performance management, talent management, process improvements).

The Experience, Skills and Abilities Needed

Required

  • Bachelor’s degree in Mechanical, Electrical, Chemical Engineering or relevant engineering discipline.
  • Minimum of 7 years’ experience in manufacturing environment or similar.
  • Exposure to project / program management skills required

 

Preferred: 

  • Masters in an engineering discipline, MBA.
  • Experience in more than one of the following functional areas: Operations, Supply Chain, Quality.
  • Six Sigma Experience.
  • Experience in LEAN Methodologies.
  • Project Management Professional (PMP) certification.

  Other:

  • Must have excellent leadership, interpersonal and influencing skills and have a demonstrated the potential to lead a team of technical resources toward a common goal.  Demonstrated leadership aptitude toward conflict resolution, assertiveness and negotiation skills required. 
  • Demonstrated proficiency in driving continuous improvement for performance, quality, time, and cost; strong planning and organization skills required.
  • Ability to work in a highly regulated environment.
  • Demonstrated ability to make sound data driven decisions; Understand, track, drill down and question activities and issues in all functional area. Strong attention to detail, follow-through skills
  • Sets the standard for timeliness, work ethic, and personal integrity
  • Must have basic project management skills and the ability to manage multiple inputs and project tasks.
  • Must have excellent written communication skills – reports, presentations.

What STERIS Offers

We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future.

 

Here is just a brief overview of what we offer:

  • Market Competitive pay
  • Extensive Paid Time Off and added Holidays
  • Excellent Healthcare, Dental and Vision benefits
  • Long- and Short-Term Disability coverage
  • 401(k) with a company match
  • Maternity and Paternity Leave
  • Additional add- on benefits / discounts for programs such as Pet Insurance
  • Tuition Reimbursement and continuing education programs
  • Excellent opportunities for advancement in a stable long-term career

 

#LI-MO1

#LI- Onsite

Pay range for this opportunity is $116,237.50 - $136,750. This position is eligible for bonus participation.

 

Minimum pay rates offered will comply with county/city minimums, if higher than range listed.  Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.

 

STERIS offers a comprehensive and competitive benefits portfolio.  Click here for a complete list of benefits: STERIS Benefits

 

Open until position is filled.

 

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit www.steris.com.

 

If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.

 

STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.

 

The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.




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