Manufacturing Engineer (Onsite - Columbia, MO)

SolventumColumbia, MO
Onsite

About The Position

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. This position is scheduled to transfer to a local subsidiary of Thermo Fisher Scientific Inc. (Thermo Fischer). By joining Solventum during this transitional period, you will be able to work alongside an energized and mission-driven team who is experiencing this transition along with you. Until the transfer is complete, you will be employed by Solventum, and your employment is subject to all applicable terms and conditions as outlined in our employment agreement and company policies. 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.

Requirements

  • Bachelor’s degree or higher in a science or engineering discipline (completed and verified prior to start)
  • Two (2) years of combined experience in manufacturing and/or engineering 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

  • Experience in process validation (IQ/OQ/PQ)
  • Demonstrated project leadership abilities on highly technical and complex projects
  • Ability to lead and contribute across a multi-disciplinary team
  • Excellent problem solving and analytical skills
  • Experience in Lean Six Sigma/Quality Improvement
  • Excellent communication skills (oral, written and presentation)
  • Microsoft Office proficient

Responsibilities

  • Providing support and leadership for the manufacture of market leading biopharma processing filters
  • Identifying, Initiating, recommending, and leading projects to improve product cost, service, quality, process safety, and health/environmental impact
  • Performing and guiding technical and validation activities related to new product development and product line extensions.
  • Leading problem-solving events to determine root causes and implementing corrective actions to prevent recurrence
  • Monitoring and improving manufacturing operations using Lean Six Sigma tools and methodology (design of experiments, statistical process control, lean management system, kaizens, DMAIC)
  • Working closely with production and maintenance teams to perform troubleshooting and resolve equipment/downtime issues
  • Leading and executing projects for new production lines and new products
  • Corporate policies, procedures and security standards are complied with while performing assigned duties.

Benefits

  • Medical, Dental & Vision
  • Health Savings Accounts
  • Health Care & Dependent Care Flexible Spending Accounts
  • Disability Benefits
  • Life Insurance
  • Voluntary Benefits
  • Paid Absences
  • Retirement Benefits
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