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An established industry player is seeking a Production Operations Lead to guide a team in achieving daily production goals. This role involves executing production plans, training staff, and ensuring compliance with FDA and ISO regulations. If you thrive in a leadership position and are passionate about manufacturing excellence, this is your chance to make a significant impact in a dynamic environment. Join a collaborative team dedicated to advancing healthcare through innovative diagnostic tools and enjoy a comprehensive benefits package while contributing to meaningful projects.
Wondering what’s within Beckman Coulter Diagnostics? Take a closer look.
For over 80 years, we have been dedicated to advancing and optimizing laboratories to move science and healthcare forward. Join a team where you are heard, supported, and encouraged to be yourself. We celebrate diverse backgrounds, experiences, and perspectives, and are invested in your career development, creativity, and success.
Beckman Coulter Diagnostics is part of a community of six Diagnostics Companies at Danaher, working at the pace of change to improve patient lives with innovative diagnostic tools addressing major health challenges.
The Production Operations Lead for Beckman Coulter Diagnostics is responsible for supporting daily production needs, including scheduling via visual management, training associates, troubleshooting issues, and managing work performance. The role involves guiding a team to meet daily production goals, with potential plan adjustments to stay on track.
This position is a key part of the Hardware Manufacturing Team and reports to the Supervisor of Production Operations. It is based in Chaska, MN. If you thrive in a leadership role within a multifunctional environment and aim to build a top-tier manufacturing organization, read on!
In this role, you will have the opportunity to:
Execute daily production plans to meet deadlines and quality standards.
Maintain organization and training plans for the work area.
Train staff according to SOPs, following engineering drawings, work orders, and specifications while adhering to FDA requirements.
Ensure compliance with FDA QSR, GMP, and ISO regulations.
Collaborate with cross-functional teams to troubleshoot and emphasize quality.
Identify and recommend quality improvements in production methods, equipment, and efficiency.
Participate in lean manufacturing initiatives.
The essential requirements of the job include:
High School diploma with 7+ years of experience.
Experience in a regulated industry (preferred, e.g., FDA, ISO).
Proficiency in Microsoft Office applications and basic Windows OS.
Preferred additional experience includes:
Problem solving skills
Participation in team projects
Knowledge of Lean concepts
The hourly pay range is $25 - $29, subject to change. The role may include bonus or incentive pay. We offer comprehensive benefits, including paid time off, insurance, and a 401(k).
Join us to help accelerate the impact of science and technology. For more information, visit www.danaher.com.
We are committed to equal opportunity employment and value diversity in our workforce. Reasonable accommodations are available for applicants with disabilities. Contact us at applyassistance@danaher.com for assistance.