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Associate Director, MS&T Compliance
Associate Director, MS&T ComplianceMariana Oncology • Watertown, MA, US
Associate Director, MS&T Compliance

Associate Director, MS&T Compliance

Mariana Oncology • Watertown, MA, US
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Job Description

Job Description

Salary : Reporting :

Director, Manufacturing Science & Technology

Description :

We are seeking an experienced Associate Director, MS&T Compliance to join Marianas Manufacturing Science & Technology organization, advancing personalized medicine and radiopharmaceuticals. This role will provide leadership in compliance for manufacturing activities, with a strong focus on deviation investigations, change management, root cause analysis, and inspection readiness. The Associate Director will serve as a subject matter expert in cGMP manufacturing compliance, ensuring operational excellence, continuous improvement, and alignment with regulatory expectations in the radiopharmaceutical sector. This position will also manage compliance-related projects and act as the primary MS&T representative in interactions with Quality functions.

Illustrative Breadth of Responsibilities :

  • Lead and oversee investigation activities for deviations, including coordination of cross-functional teams and impact assessments.
  • Develop and author change controls, deviation reports, root cause analyses, corrective and preventive action (CAPA) plans, and other compliance documentation.
  • Drive the timely closure of investigations, CAPAs, and change controls in close collaboration with Quality and MS&T leadership.
  • Manage ongoing MS&T compliance projects to ensure alignment with quality and regulatory requirements, while driving continuous improvement initiatives.
  • Deliver training to MS&T, Manufacturing, and Support teams on investigation best practices, root cause analysis, and CAPA effectiveness.
  • Provide inspection readiness support for both personnel (training, responses, mock inspections) and facilities (equipment, documentation, and cleanliness).
  • Identify compliance risks within GMP manufacturing operations and recommend process improvements aligned with Right-First-Time principles.
  • Support and execute risk assessments, gap analyses, and compliance-focused operational reviews.
  • Serve as the MS&T compliance representative during audits, inspections, and management review presentations.
  • Act as the key liaison between MS&T and local / parent company Quality Assurance functions, ensuring alignment on compliance priorities, strategies, and execution.
  • Partner with cross-functional teams to strengthen operational and regulatory compliance across MS&T activities.
  • Other duties as assigned.

Requirements / Skills :

  • Bachelors degree in Life Sciences, Engineering, or related field; advanced degree preferred.
  • 8+ years of experience in MS&T, Process Development, or Manufacturing within the pharmaceutical, biotechnology, or radiopharmaceutical industry.
  • Strong expertise in deviation management, CAPA systems, change control processes, and GMP compliance frameworks.
  • Working knowledge of bioprocessing workflows including upstream, downstream, and analytical operations.
  • Demonstrated ability to analyze complex technical data and drive data-based decision-making.
  • Strong scientific and engineering aptitude with proven problem-solving and compliance investigation skills.
  • Excellent written and verbal communication, including the ability to present to auditors, inspectors, and senior leadership.
  • Proven track record in training and developing technical staff in compliance and investigation best practices.
  • Experience with electronic quality management systems (e.g., Veeva), ERP platforms, and statistical tools (e.g., JMP, SIMCA) strongly preferred.
  • In-depth understanding of regulatory requirements (FDA, EMA, ICH) in a GMP manufacturing environment.
  • Mariana Oncologys Principles

  • Building a Legacy
  • Execution Excellence
  • Courage of our Convictions
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