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Sartorius

Bioprocess and laboratory solutions provider

Manager of Quality Systems

Regulatory & Quality (Life Sciences)Posted on Nov 10
Full-timeYauco, Puerto RicoNo salary listed

About the Job

Requirements

  • A bachelor's degree in Engineering, Life Sciences, or a related discipline is required; an advanced degree is preferred.
  • At least 10 years of progressive experience within a GMP-regulated environment is required, preferably in the medical device industry under 21 CFR Part 820.
  • At least 5 years of leadership or supervisory experience managing cross-functional teams is required.
  • Hands-on experience managing and improving Quality Systems, including CAPA, Change Control, Document Control, and Complaints, is required.
  • Strong knowledge of global quality regulations and standards, including ISO 9001, ISO 13485, and FDA requirements, is required.
  • Proven ability to lead internal, customer, and regulatory audits and ensure sustained compliance is required.
  • Experience in KPI-driven quality performance management and continuous improvement methodologies is required.
  • Strong analytical and problem-solving skills with a data-driven decision-making approach are required.
  • Ability to identify improvement opportunities and drive efficiency, cost reduction, and process optimization is required.

Responsibilities

  • Oversee and maintain the effectiveness of the site’s Quality Management System in alignment with Sartorius standards and applicable regulatory requirements.
  • Ensure systematic management and analysis of customer complaints, driving structured problem-solving and continuous improvement initiatives.
  • Lead the definition, monitoring, and review of key performance indicators (KPIs), and facilitate KPI-driven meetings to reinforce a quality-focused culture, improve processes, and measure performance outcomes.
  • Oversee equipment and instrument calibration programs to ensure accuracy, compliance, and operational reliability.
  • Serve as the primary lead for customer audits, ensuring readiness, coordination, and effective execution.
  • Manage audit outcomes by implementing corrective and preventive actions (CAPAs) to address findings and strengthen the overall quality system.
  • Lead and oversee all customer, internal, and regulatory audits, ensuring compliance with applicable standards and timely closure of findings.
  • Maintain and continuously improve compliance with ISO 9001, ISO 13485, and RX-360 certifications.
  • Ensure customer observations and complaints are communicated, assigned, and resolved within defined timelines.
  • Drive root cause analysis and corrective actions to achieve timely complaint closure in accordance with company standards.
  • Develop and implement strategies to achieve zero customer complaints and ensure closure adherence within 30 days.
  • Own and manage core Quality System processes, including CAPA, Nonconformance (NCPR), Change Control, and Document Control.
  • Monitor system effectiveness through KPIs and metrics, driving continuous improvement initiatives.
  • Ensure governance and lifecycle management of controlled documents.
  • Manage and develop the Document Control and Complaint Handling teams to ensure operational excellence and compliance.
  • Foster a culture of quality, accountability, and continuous improvement across the organization.
  • Oversee the site-wide calibration program to ensure accuracy of measurement systems and regulatory compliance.
  • Collaborate with Manufacturing and cross-functional teams to enhance product reliability, efficiency, and cost-effectiveness.
  • Identify opportunities to reduce waste, improve efficiency, and optimize quality processes.
  • Define, track, and report key quality KPIs to drive performance and informed decision-making.
  • Develop action plans to reduce CAPA and NCPR volumes and improve overall system effectiveness.
  • Support customer satisfaction initiatives and internal engagement programs, driving measurable improvements.
  • Act as a key advocate for quality excellence in customer-facing and internal processes.
  • Establish and maintain quality objectives aligned with business strategy and regulatory requirements.
  • Ensure quality goals align with production processes to support scalability, compliance, and operational excellence.

Desired Qualifications

  • Medical device industry experience, preferably involving 21 CFR Part 820.
  • An advanced degree.

About the Company

Sartorius

Bioprocess and laboratory solutions provider

Sartorius provides laboratory and bioprocessing equipment and services for biopharmaceutical development and manufacturing. Its products cover end-to-end needs such as bioreactors, single-use technologies, filtration and purification tools, analytics, and lab instruments, enabling researchers to grow, purify, and test biologics. The company differentiates itself with a long history, a broad, integrated portfolio, global support, and strategic acquisitions that expand its services under one trusted partner. Its goal is to help biopharmaceutical companies develop and produce biotech drugs and vaccines reliably at scale.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Göttingen, Germany
Founded
1870

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