Merck-posted 11 days ago
$77,000 - $115,600/Yr
Full-time • Mid Level
Miamisburg, OH

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: Supervise all day-to-day Quality Control activities, including product testing, quality data analysis, resource allocation, and ensuring compliance with regulatory requirements, specifications, and customer demands. Responsible for overall team performance, actively leading, mentoring, coaching, and developing QC specialists. This includes fostering engagement, ensuring training, and driving talent development across functions. Ensure rigorous adherence to safety culture, work practices, and quality regulations. Proactively use data and risk assessments to pre-empt injuries and quality non-conformances. Foster a culture of continuous improvement within the QC team, identifying inefficiencies, optimizing test methods, implementing streamlined protocols, and championing global quality initiatives. Facilitate effective communication and collaboration with other departments (e.g., Production, Engineering) to drive shared ownership of quality outcomes, align on expectations, and integrate QC processes seamlessly. Possess strong problem-solving skills, with the ability to analyze quality data, identify trends, root causes, and areas for improvement, using data analytics to inform decisions and prevent deviations. Empower and develop autonomous production teams by collaborating cross-functionally and upskilling production operators and process engineers in quality requirements to facilitate local decision-making. Encourage and enable the development of key functional capabilities within the team, positioning the QC function as a strategic driver of success, innovation, and enhanced performance within the organization.

  • Supervise all day-to-day Quality Control activities, including product testing, quality data analysis, resource allocation, and ensuring compliance with regulatory requirements, specifications, and customer demands.
  • Responsible for overall team performance, actively leading, mentoring, coaching, and developing QC specialists.
  • Ensure rigorous adherence to safety culture, work practices, and quality regulations.
  • Proactively use data and risk assessments to pre-empt injuries and quality non-conformances.
  • Foster a culture of continuous improvement within the QC team, identifying inefficiencies, optimizing test methods, implementing streamlined protocols, and championing global quality initiatives.
  • Facilitate effective communication and collaboration with other departments (e.g., Production, Engineering) to drive shared ownership of quality outcomes, align on expectations, and integrate QC processes seamlessly.
  • Possess strong problem-solving skills, with the ability to analyze quality data, identify trends, root causes, and areas for improvement, using data analytics to inform decisions and prevent deviations.
  • Empower and develop autonomous production teams by collaborating cross-functionally and upskilling production operators and process engineers in quality requirements to facilitate local decision-making.
  • Encourage and enable the development of key functional capabilities within the team, positioning the QC function as a strategic driver of success, innovation, and enhanced performance within the organization.
  • Bachelor’s Degree in Chemistry, Biology, or other Life Science discipline.
  • 2+ years of work experience in Analytical Chemistry.
  • 3+ years of quality control experience.
  • 3+ years of e xperience with ISO and cGMP quality standards.
  • 2+ years of leadership or supervisory experience.
  • Master’s Degree or PhD in Chemistry.
  • Strong communication and problem-solving skills.
  • Experience in chemistry (emphasis on analytical and organic) combined with strong business aptitude and ability to apply risk-benefit analysis.
  • health insurance
  • paid time off (PTO)
  • retirement contributions
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