Associate Director, Quality Assurance

MSD•Upper Gwynedd Township, PA

1d•$142,400 - $224,100•Onsite

About The Position

The West Point Quality organization ensures our products are manufactured, processed, tested, packaged, stored, and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. The Associate Director, Inspections lead will be a core member of the West Point Quality Assurance Leadership Team and serves as a quality leader accountable for the quality oversight and management of the Quality team overseeing Regulatory Inspections and Health Authority reporting supporting the West Point Manufacturing and Quality Control laboratories. The position will be responsible to ensure site’s compliance with applicable regulations, industry standards and Quality Management Systems. The incumbent will be responsible for developing, implementing and leading a group of compliance professionals through the deployment of compliance programs, monitor compliance efforts and advise site senior management on compliance related matters. The role involves serving as the lead for regulatory agency inspection coordination and collaborating with other departments to address compliance issues. The responsibilities of this role will additionally include sustainment through continuous improvement of the organization at the site.

Requirements

Applicable experience, strong understanding and knowledge of relevant quality systems expectations in the biotechnology or vaccine industry.
Expert knowledge of cGMP relevant to the biotechnology or vaccine industry including knowledge of the local and international GMP regulations.
In-depth knowledge of regulatory requirements and guidelines (e.g. 21 CFR part 11, Annex 11).
Ability to work independently while fostering collaboration in team settings and matrix organizations to achieve common goals.
Highly skilled in listening to diverse perspectives, developing impactful solutions, and advocating for effective positions through influence.
Strong working knowledge of Quality Management Systems, and associated business processes.
Excellent communication, leadership, technical writing and problem-solving skills.
Ability to cultivate positive, transparent, and productive relationships across various stakeholders.
A team player with high initiative, demonstrated planning skills, proven performance in problem-solving, team building and staff development.
Experience in working with cross functional teams as well as good leadership skills in a matrix organization.
Experience in managing cross-functional initiatives or programs.
Bachelor’s degree (BS) or Master’s degree (MS) with Ten (10) years applied professional work experience in one of the following pharmaceutical work areas: quality assurance, compliance, manufacturing operations, technical operations.
Change Management
Computer System Validation (CSV)
Decision Making
Driving Continuous Improvement
GMP Laboratory
People Leadership
Performance Qualification (PQ)
Quality Auditing
Quality Control Documentation
Quality Management Standards
Quality Management Systems (QMS)
Quality Risk Management
Regulatory Compliance
Supplier Quality Management
Training and Development

Nice To Haves

Experience leading regulatory inspection readiness and Health Authority inspections in a pharmaceutical, biotech, or vaccine environment.
Strong knowledge of quality systems, compliance oversight, and CAPA management.
Demonstrated ability to lead cross-functional initiatives in a matrix environment.
Experience interacting with regulatory agencies and senior leadership.
Strong understanding of health authority reporting, complaint management, and market action processes.
Ability to interpret complex regulations and translate them into practical site-level actions.
Proven leadership, coaching, and team development skills.
Excellent communication, influence, and relationship-building skills.
Strong organizational and problem-solving skills with a continuous improvement mindset.
Experience driving simplification, standardization, and process improvement across a site.

Responsibilities

Develop and implement comprehensive compliance program for the site to ensure Permanent Inspection Readiness (PIR), which includes Health Authority Reporting and inspection readiness team.
Track and Interpret changes in regulations, industry standards and ensure proactive awareness and PIR at the site.
Conduct regular compliance risk assessments, identify potential risks and develop strategies to mitigate the risks.
Identify and address compliance issues, develop corrective action plans and implement improvements to compliance programs.
Act as a liaison and/or SME to present operational compliance to Health Authorities and regulatory agencies on relevant topics.
Lead a team of professionals who serve as contact for regulatory agencies during inspections, responding to inspectional or regulatory agency inquiries, providing information and addressing compliance concerns.
Serve as Manager to the lead for the team coordinating Health Authority reporting, Market action events, and complaint process management for the site.
Provide training and guidance to employees on compliance related matters, ensuring a robust PIR at the site.
Provide expertise in developing strategies for inspection readiness including working with Regulatory with relevant submissions for new product launches.
Engage and drive continuous improvement initiatives across the site to drive simplification and standardization.