Production Supervisor (Second shift)

Cordis•Irvine, CA

9h•$76,450 - $102,300•Onsite

About The Position

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs. The Production Supervisor (Second shift) will manage daily staffing needs of the manufacturing lines to optimize overall team's quality, effectiveness, efficiency, and output. You will also track and report overall team/shift performance in key metrics, lead and manage manufacturing teammates, and coordinate with other stakeholders to ensure that the production plan goals are met and to ensure that the production process delivers high quality products meeting the product specifications. Key Accountabilities: Daily presence in CER; provide supervision and performance management of Manufacturing Teammates, including both day‐to‐day feedback and annual review process. Oversee ongoing day‐to‐day resource allocation for line production and related activities (including capacity planning and performing time studies) Develop Manufacturing Teammates to increase their effectiveness in the organization (i.e. cross-training) Schedule production builds to meet daily/weekly/monthly goals. Inform management of scheduling or production problems as they arise; develop potential resolutions to issues and work with support teams to correct issues. Work on various production issues where analysis of the situation or data requires determination and review of relevant factors. Exercise judgment within defined company procedures and policies to determine appropriate action. Initiate, develop, and drive implementation of procedures and processes needed to improve manufacturing quality/output/yields/etc. Identify potential production issues and develop solutions to prevent recurrences. Initiate, analyze data, and perform root cause investigation or tasks for NCMRs (Non‐Conforming Material Reports) and CAPA (Corrective Action, Preventative Action) Troubleshoot issues with minimal help from support groups; demonstrate initiative and a high level of problem-solving skills Champion Lean, cGMP, 5S, and QSR concepts and procedures Lead and manage projects (as assigned). Develop resources to accomplish tasks and manage timelines to meet project goals Develop training programs for new Manufacturing Teammates and coordinate training to revisions/new releases of documentation Update procedures (as necessary) to ensure compliance with existing processes/new processes Provide feedback to R&D and Engineering groups during project/engineering builds Supervise Manufacturing Teammates in multiple production areas; backfill for other supervisors when on vacation, etc. Working closely with Manufacturing Manager, lead and manage Manufacturing Teammates while coordinating with other stakeholders to execute the production plan. Strategic Impact: The Production Supervisor is key in ensuring adherence to the production build schedule to achieve company goals and objectives. This role also champions key essential Production and Quality philosophies and methodologies on the Production floor (emphasizing in Quality, efficiency, etc.).

Requirements

AA degree required. A bachelor’s degree in technical discipline (engineering, math, or science) is preferred.
A minimum of four years’ experience supervising in a highly regulated manufacturing environment is required. Medical device manufacturing experience is highly preferred.
Experience implementing Lean Manufacturing concepts and/or catheter manufacturing is preferred.
Experience working inside a controlled room environment (i.e. cleanroom)
Focused attention to detail and the ability to work in a fast-paced changing environment is key.
Strong project management skills.
Requires excellent communication skills (both written and spoken) and possess strong capabilities in managing, coaching, and training talent.
Ability to establish a culture of positive reinforcement while also being comfortable administering disciplinary actions (as required).
Fluent in English
Able to work in a controlled manufacturing environment (i.e. cleanroom).
Must be able to lift and carry up to 50 lbs.
US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.

Nice To Haves

A bachelor’s degree in technical discipline (engineering, math, or science) is preferred.
Medical device manufacturing experience is highly preferred.
Experience implementing Lean Manufacturing concepts and/or catheter manufacturing is preferred.

Responsibilities

Daily presence in CER; provide supervision and performance management of Manufacturing Teammates, including both day‐to‐day feedback and annual review process.
Oversee ongoing day‐to‐day resource allocation for line production and related activities (including capacity planning and performing time studies)
Develop Manufacturing Teammates to increase their effectiveness in the organization (i.e. cross-training)
Schedule production builds to meet daily/weekly/monthly goals. Inform management of scheduling or production problems as they arise; develop potential resolutions to issues and work with support teams to correct issues.
Work on various production issues where analysis of the situation or data requires determination and review of relevant factors. Exercise judgment within defined company procedures and policies to determine appropriate action.
Initiate, develop, and drive implementation of procedures and processes needed to improve manufacturing quality/output/yields/etc.
Identify potential production issues and develop solutions to prevent recurrences.
Initiate, analyze data, and perform root cause investigation or tasks for NCMRs (Non‐Conforming Material Reports) and CAPA (Corrective Action, Preventative Action)
Troubleshoot issues with minimal help from support groups; demonstrate initiative and a high level of problem-solving skills
Champion Lean, cGMP, 5S, and QSR concepts and procedures
Lead and manage projects (as assigned). Develop resources to accomplish tasks and manage timelines to meet project goals
Develop training programs for new Manufacturing Teammates and coordinate training to revisions/new releases of documentation
Update procedures (as necessary) to ensure compliance with existing processes/new processes
Provide feedback to R&D and Engineering groups during project/engineering builds
Supervise Manufacturing Teammates in multiple production areas; backfill for other supervisors when on vacation, etc.
Working closely with Manufacturing Manager, lead and manage Manufacturing Teammates while coordinating with other stakeholders to execute the production plan.