Easter Seals Jobs

Overview

Cordis is a pioneering medical technology company specializing in groundbreaking solutions for cardiovascular and peripheral vascular diseases. Our flagship product, SELUTION, combines pharmaceuticals with a traditional balloon catheter, revolutionizing treatments for coronary and peripheral artery diseases. With four Investigational Device Exemptions (IDEs) approved and actively enrolling patients (Coronary ISR, Coronary De Novo, Peripheral SFA, and Peripheral BTK), Cordis is leading the way in delivering transformative medical solutions.

If you love a challenge and are ready to have a direct, positive impact on the lives of millions, then this is the place for you. Join us, and let’s improve the wellbeing of millions, together.

We are the people behind the people who keep saving lives.

Manage daily staffing needs of the manufacturing lines to optimize overall team's quality, effectiveness, efficiency, and output. 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.

Responsibilities

1.1. 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 determining 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 cGMP and QSR concepts and procedures

• Champion 5S principles

• Champion Lean Manufacturing principles

• 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.

• Multi‐task (as needed) in a fast‐paced environment

• Working closely with Manufacturing Manager, lead and manage Manufacturing Teammates while coordinating with other stakeholders to execute the production plan.

1.2. 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.).

1.3. Key Interactions:

Supervisor : Manufacturing Manager

Direct Reports: 25+ Manufacturing Operators

Key Suppliers : Supply Chain/Materials, Quality Assurance, Manufacturing Engineering

Key Customers : Commercial Product Planning, R&D, Clinical

Qualifications

Education and Work Experience:

• AA degree required. A bachelor’s degree in a 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.

• Results orientated, accountable, and willingness to own projects and drive them to timely completion.

• 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).

Competencies & Skills:

• Precise, Rigorous, Detail-Oriented

• Team Leader, ability to inspire and support a team.

• Strong communication skills.

• Supportive, keen to promote quality through example and continuous support.

• Global, International Orientation

• Ability to take independent decisions

• Fluent in English

Physical Requirements:

• Able to work in a controlled manufacturing environment (i.e. cleanroom).

• Must be able to lift and carry up to 50 lbs.

Working Hours

1st shift production: 6:00 am to 2:30 pm (with 30 min break)

Note: This position may be requested to supervise 2 nd shift production, 2:00 pm to 10:30 pm (with 30 min break), as required. The time could be variable due to potential OT.

Pay / Compensation

The expected pre-tax pay rate for this position is $73,700 - $99,000 per year

Actual pay may fluctuate outside of the listed range depending on skills, education, experience, job-related knowledge and location.

US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa.

Cordis is proud to be an equal opportunity employer and is committed to providing equal opportunity for all teammates and applicants. At Cordis, our teammates all bring different strengths, experiences, and backgrounds, who share a passion for improving people's lives. Diversity not only includes race and gender identity, but also age, disability status, veteran status, sexual orientation, religion, and many other parts of one’s identity. All our teammate’s points of view are key to our success, and we believe inclusion is everyone's responsibility. Together, we strive to create and maintain working and learning environments that are inclusive, equitable and welcoming.

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Job Locations US-CA-Irvine

ID 2024-3296

Category Manufacturing

Position Type Regular Full-Time

CORDIS is proud to be an equal opportunity employer, values diversity in all its forms is and committed to fostering an inclusive work environment. We are committed to advancing our culture of belonging, where all teammates feel seen, heard, and appreciated and encouraged to be their authentic selves. Our team is invested in attracting, retaining and growing top talent. Our Teammates are the core of our innovation and success. Cordis is an inclusive, engaging place to work and grow a career. CORDIS is committed to offering reasonable accommodations, upon request, to job applicants with disabilities. If you need assistance or an accommodation due to a disability, please contact GlobalHR@Cordis.com