Director of Quality

The businesses of Merck KGaA, Darmstadt, Germany•Jaffrey, NH
•$154,700 - $290,300

About The Position

MilliporeSigma is seeking a senior site quality leader to lead an approximately 200-person, multi-function Quality organization at a high-complexity Life Science manufacturing site. The role sits on the site leadership team and is responsible for setting the quality vision, establishing strategic direction, and driving day-to-day execution across Quality Assurance, Quality Control laboratories, Quality Systems, Compliance, Supplier Quality, Audits, CAPA, product release and disposition, customer complaint resolution, and data integrity. The Director leads through a team of managers and is accountable for talent development, organizational design, and succession planning across the Quality function. Responsibilities include owning the quality budget, making business and resourcing trade-offs, and governing site-level quality KPIs visible to site and regional leadership. The role requires sound risk-based decisions under pressure, including during regulatory inspections, remediation programs, and complex deviation or CAPA investigations, as well as a track record of measurable Quality and organizational transformation. The Director champions digital quality initiatives to strengthen data integrity and operational efficiency, and partners with production, technical services, and commercial functions to integrate quality throughout operations—from supplier qualification and environmental monitoring to product release and customer complaint resolution. This leadership shapes audit readiness, inspection outcomes, and continuous improvement, with an impact on compliance performance and customer satisfaction. The role does not offer work-authorization sponsorship; external applicants must be eligible to work in the United States.

Requirements

  • Bachelor’s degree in Engineering, Applied Engineering, Sciences, or a related field.
  • 10 or more years of progressive experience in quality management within a regulated manufacturing environment.
  • Demonstrated leadership of a multi-function Quality organization at meaningful scale, leading through managers rather than solely as an individual technical contributor.
  • Proven experience leading regulatory inspections, such as FDA or EMA inspections, including remediation efforts and difficult, risk-based decisions under pressure.

Nice To Haves

  • Advanced degree in a relevant scientific or engineering discipline.
  • Experience owning full Quality scope, including Quality Assurance, Quality Control, Quality Systems, Compliance, Supplier Quality, Audits, CAPA, product release and disposition, and data integrity.
  • Experience managing a quality budget and governing site-level quality performance metrics.
  • Demonstrated leadership of measurable Quality or organizational transformation, with evidence of sustained improvement in compliance outcomes.
  • Professional certifications in quality or regulatory frameworks such as Six Sigma Black Belt, ASQ, GMP, GLP, or GxP.
  • Experience with quality management systems including ISO 9001, ICH Q9, and GMP in a Life Science manufacturing environment.
  • Expertise in risk management, deviation handling, CAPA processes, and continuous improvement methodologies.
  • Experience with digital quality platforms, electronic quality management systems, ERP platforms, and audit management tools.
  • Familiarity with material analysis tools such as FTIR, DSC, microscopy, particle counters, and integrity testing.
  • Understanding of validation and qualification processes, FMEA, SPC, sampling plans, and change control in regulated environments.

Responsibilities

  • Lead an approximately 200-person, multi-function Quality organization at a high-complexity Life Science manufacturing site.
  • Set the site quality vision and strategic direction, and drive day-to-day execution across Quality Assurance, Quality Control laboratories, Quality Systems, Compliance, Supplier Quality, Audits, CAPA, product release and disposition, customer complaint resolution, and data integrity.
  • Lead through a team of managers and oversee talent development, organizational design, and succession planning for the Quality function.
  • Own the quality budget and make business and resourcing trade-offs.
  • Govern site-level quality KPIs visible to site and regional leadership.
  • Make risk-based decisions under pressure, including during regulatory inspections, remediation programs, and complex deviation or CAPA investigations.
  • Lead regulatory inspections and remediation efforts.
  • Champion digital quality initiatives that strengthen data integrity and operational efficiency.
  • Partner with production, technical services, and commercial functions to integrate quality throughout operations.
  • Drive audit readiness, inspection outcomes, and continuous improvement to improve compliance performance and customer satisfaction.

Benefits

  • Health insurance
  • Paid time off (PTO)
  • Retirement contributions
  • Other perquisites
  • Position may be eligible for sales or performance-based bonuses.
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