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Operations Supervisor, Manufacturing (2nd Shift)

Stryker
Posted 11 days ago, valid for 22 days
Location

Irvine, CA 92614, US

Salary

$102,700 - $171,100 per year

Contract type

Full Time

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Sonic Summary

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  • Stryker is seeking an Operation Supervisor for Manufacturing (2nd Shift) in Irvine, CA, focusing on the Peripheral Vascular division.
  • The role requires a Bachelor's degree and at least 4 years of experience in business, operations, or manufacturing, preferably in the medical device industry.
  • Key responsibilities include managing production activities, ensuring quality compliance, and leading continuous improvement initiatives.
  • The salary for this position ranges from $102,700 to $171,100 USD, with a travel percentage of 10%.
  • Candidates should possess strong leadership skills and a working knowledge of quality systems and business processes.
Work Flexibility: Onsite

What you will do:

Stryker is hiring an Operation Supervisor, Manufacturing (2nd Shift). This role will support our Peripheral Vascular (PV division) and is an onsite role in Irvine, CA. In this role, you will be responsible for operations activities related to the manufacturing of medical devices. You will also be responsible for producing, tracking, and managing the associated metrics, including Quality, Customer Service, Cost, People Development, and Innovation. You will focus on leading the team to create the Quality First Culture and meet quality expectations, drive Lean effort and team engagement to meet the overall business result, and provide business growing support such as manufacturing transfer and new product development. Additional responsibilities include:

  • Lead, oversee, coordinate, and facilitate the activities in a production area ensuring safety, quality, and compliance while achieving production goals, efficiency and yield targets and cost objectives.
  • Manage self and team in a manner that demonstrates a primary commitment to patient safety, product quality and compliance with the Stryker, Quality Manual, and its governing regulations. Ensure product is manufactured to the most current/validated method/process and specification and DHR for every lot is correctly filled in per GMP & QS requirements.
  • Proactive capacity management (Staffing and equipment) with associated inter-disciplinary coordination. Make budgetary recommendations on capital expenditures and direct labor resource planning.
  • Work with planning team Ensure appropriate build scheduling and execute to meet customer requirements.
  • Ensure traceability and inventory accuracy/control including components, sub-assemblies and finished goods.
  • Provide strong supervision of human resources including recruiting, interviewing, hiring, development and performance management, improve the organization capability for the responsible area.
  • Lead the team create a respect, open communication, positive and collaborative work environment.
  • Lead or participate Continuous Improvement projects by leverage Lean Light house, Kaizens, and other lean methodology to improve quality, increasing capacity, improving efficiency, reducing scrap improve space utilization and other activities as business needs.
  • Ensure equipment, tools, fixtures, gages and measuring devices are effectively used, maintained, and calibrated in responsible area.
  • Interact with Manufacturing Engineering, Equipment Engineering, Quality, and materials colleagues to drive results with highly efficiency and effectiveness.
  • Participate in quality systems audits (i.e., internal & external)
  •  Participate in budget process and manage the budget implementation for the responsible area.
  • Must have ability to lift 50 pounds routinely; 75 pounds occasionally.

What you need:

  • Bachelor’s degree in a technical or business-related discipline.
  • 4+ years' experience in business, operations, or manufacturing, preferably in medical device or other highly regulated industry.
  • Working knowledge & understanding of general Quality System & ISO 9001 requirements.
  • Working knowledge and understanding the overall business process from material receiving to finish goods shipping.
  • Ability to read, analyze and interpret general business periodicals, professional journals, and technical procedures. Ability to author reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions. Must have the ability to communicate and understand technical terminology.
  • Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Must have the ability to resolve daily production problems.
  • Understanding of team dynamics, and ability to maximize organizational results.
  • Self-starter with the ability to accomplish tasks with minimal supervision.
  • Demonstrated effective interaction skills across multi-disciplinary functions (lateral & upward/downward).
  • 3+ years' experience in a supervisory role preferred.
  • Lean/Six Sigma experience preferred.
  • System experience such as NetSuite, SAP, MES preferred.

  

 

$102,700 - $171,100 USD

  

 

Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.



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By applying, a Stryker account will be created for you. Stryker's Privacy Policy and Terms & Conditions will apply.

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