Supervisor Reagent Manufacturing - Carlsbad, United States - Beckman Coulter Diagnostics
Description
Wondering what's within Beckman Coulter Diagnostics? Take a closer look.
At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward.
Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.
Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher.Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges.
The
Reagent Manufacturing Supervisor for Beckman Coulter Diagnostics will lead manufacturing area by owning capacity, productivity, and continuous improvement efforts to meet long-term profitability targets.
You would report to the Value Stream Manager responsible for leading the Diagnostics Reagents production team. If you thrive in a fast-paced, dynamic role and want to work to build a world-class manufacturing organization—read on.
In this role, you will have the opportunity to:
- Ensure that manufacturing schedule is generated and adhered to, mitigating issues as needed.
- Support departmental and site KPI's, including associate/team Engagement, Safety, Quality, On Time Delivery, and Productivity.
- Empower associate performance to include staffing and crafting goal/development objectives.
- Identify opportunities for improvement and work with crossfunctional team to implement most impactful ones
- Utilize problem solving techniques to implement both containment, root cause analysis, and countermeasure determination and implementation.
- Take ownership for quality in area by utilizing quality guidelines, including documentation, internal quality improvement, & scrap reduction.
- Support Kanban process for material needs and own inventory reduction initiatives while managing both direct & indirect costs in the value streams.
The essential requirements of the job include:
- Bachelor's degree in Chemistry, Life Sciences or related field with 5+ years' industry experience OR a Masters degree with 3+ years' experience, OR equivalent years of applicable industry experience
- 3+ years' experience leading teams with a proven ability to develop diverse teams
- Experience working in an FDAcontrolled and/or ISO regulated environment
- Strong data analysis ability (Excel experience at a minimum)
- Crucial conversations, conflict resolution and risk management
- Experience working in a fastpaced environment working with tight deadlines
It would be a plus if you also possess previous experience in:
- Proven knowledge/usage with lean tools that help with continuous improvement: Value Stream Mapping, Standard Work, 5S, Kanban & Practical Problem Solving
- Managing projects of various complexity
- Experience with Enterprise Resource Planning software
This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting.
We may ultimately pay more or less than the posted range. This range may be modified in the future.This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note:
No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable.
The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
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