Engineering and Labeling Supervisor

SOLVENTUM • Irvine, CA

6d • $96,000 - $132,000 • Onsite

About The Position

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. As the Engineering and Labeling Supervisor you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:

Requirements

• Bachelor’s Degree or higher from an accredited institution in engineering or related discipline and (4) four years of combined experience in a leadership and/or supervisory role in a private, public, government or military environment
• Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Nice To Haves

• Proficient knowledge of Good Manufacturing Practices (GMPs)
• Project management including process improvements and technical validations
• Experience working in a large healthcare manufacturing company
• Labeling approval and implementation

Responsibilities

• Lead, coach, and mentor manufacturing and labeling engineering teams while measuring team and individual performance, setting goals and accountability.
• Drive continuous improvement initiatives to optimize processes, increase efficiency, and ensure regulatory compliance.
• Manage the documentation required for changes to manufacturing and artwork processes in a GMP environment.
• Become and act as the subject matter expert for the packaging and labeling process for medical devices.
• Oversee the management, review, approval, and phase in/phase out of labeling and packaging artwork for various products, ensuring regulatory and internal compliance.
• Lead efforts to integrate advanced technologies and automation solutions to enhance labeling and packaging processes and operational efficiency.
• Support existing product lines, as well as New Product Introduction (NPI) and manufacturing scales ups.
• Collaborating with cross functional partners such as production, planning, regulatory, quality assurance and plant engineering, to improve efficiency and effectiveness of the organization.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees