MSD
Senior Director, Quality Assurance
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Senior Director, Biologics, DP, & Device Platform Lead, Third Party Quality Management & Due Diligence (TPQM & DD), Global Development Quality
The Senior Director, Biologics, DP, & Device Platform Lead, Third Party Quality Management & Due Diligence (TPQM & DD), Global Development Quality is responsible for providing expert strategic, scientific and operational leadership to teams.
This position will lead strategic operational initiatives, build talent across the organization, and the overall operational and strategic oversight of third-party contractors and vendors providing biologic drug substance, sterile and non-sterile bulk drug product, and medical device and combination product including design and assembly in support of our Company’s clinical supply chain.
This position is responsible for a team of >9 professionals. Key areas of responsibility include defining and driving the quality performance and ensuring compliance robustness on behalf of TPQM across a designated vendor base. This includes supporting the development and execution of a strategic global vision for TPQM and influencing the same for key stakeholder in multiple business areas.
This role will provide specific quality support and be responsible for supporting the development and driving the execution of the continuous improvement of third-party quality processes within a high-impact vendor base to minimize and mitigate risk to our Company development programs.
Primary Activities:
- In-depth close collaboration with the vendor quality and technical personnel and associated interaction with their functional equivalents in the specific source area on executing against strategic objectives related to the designated vendor base.
- Navigating technically highly complex quality related matters, both process improvements and significant quality issues and events.
- Supervise a group of ~9 Quality professionals.
An advanced level of knowledge of the clinical development process and of the associated stakeholder organizations is required for this role in addition to technical and quality expertise and experience to enable the incumbent to carry the necessary level of credibility to the stakeholder areas as well as with the vendors at senior levels to be successful.
In addition to the high-level responsibilities discussed above, the incumbent is expected to independently execute on the following:
- Execute the daily operational TPQM support for the biologics drug substance and sterile and non-sterile drug product vendor bases related to the most complex activities that our Company outsources, with the associated potential for high impact to the development portfolio.
- Supporting the development of and driving the execution of quality strategies, improvement initiatives in line with business drivers and objectives.
- Provide close support to our Company’s Global Auditing group in relation to audits conducted and mitigation activities in regard to audit observations for the designated vendor base.
- Interacting cross-functionally and cross-divisionally with senior management on quality/regulatory matters as well as special projects, and externally with inspectors and colleagues in industry in relation to the designated vendor base.
- Driving the resolution of contractor / vendor related business practice, Quality and/ or compliance issues of high-impact scope and highest level of complexity on cross-functional and/ or cross-divisional basis in relation to the designated vendor base.
- Provision of in-depth technical / quality expertise re; identification of trends and/or potential compliance gaps and proactively leading the resolution of long-standing or significant issues affecting quality and efficiency.
- Where appropriate, coaching, mentoring and developing team members supporting their personal development and also colleagues in areas of expertise.
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Skills:
- Strong scientific/ technical expertise in R&D activities, coupled with the ability to interact with and influence scientific subject matter experts and senior leaders on various product initiatives and issues.
- Strong compliance knowledge and understanding of regulatory agency regulations and requirements and interpretation and application re; GMPs to a R&D environment.
- Possess deep drug development knowledge; demonstrated ability to facilitate training and learning with colleagues and apply knowledge to enhance the drug development process.
- Demonstrated knowledge of continuous improvement methodologies; ability to direct complex cross-functional initiatives.
- Demonstrated leadership, incl. strategy deployment experience, in a pharmaceutical environment.
- Proven track record of delivering tangible benefits from process improvement activities in a pharmaceutical environment.
- Demonstrated experience in quality risk management in the pharmaceutical industry.
- Strongly developed cross-functional teamwork, collaboration, influencing and negotiation skills.
- Strong demonstrated skills in communicating (oral and written) effectively with diverse individuals/groups.
- Experienced and strong people manager with proven track record of developing talent.
Education/Experience:
- Bachelor's degree in engineering, Biology, Chemistry, or related field.
- A minimum of 10+ years of relevant experience working within the pharmaceutical industry or advanced Degree with 8+ years relevant experience.
- Experience interacting with regulatory officials and external auditing parties.
Required Skills:
- Coaching
- Compliance Reporting
- Detail-Oriented
- External Manufacturing
- Leadership Theories
- Mentoring Staff
- Operational Quality
- Organizational Talent
- People Leadership
- Persuasion
- Policy Implementation
- Process Improvements
- Quality Assurance Systems
- Quality Compliance
- Quality Management
- Quality Management Systems (QMS)
- Quality Metrics
- Quality Standards
- Situational Leadership
- Stakeholder Management
- Strategic Objectives
- Supplier Auditing
- Task Allocation
- Team Collaboration
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Preferred Skills:
Compensation:
- Salary range: $173,200.00 - $272,600.00
- Eligible for annual bonus and long-term incentive, if applicable.
Benefits:
- Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
Application:
- Apply through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee).
- The application deadline for this position is 10/12/2026.
Equal Employment Opportunity:
- Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.
- Please click here if you need an accommodation during the application or hiring process.
- As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.
- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
Additional Information:
- Search Firm Representatives Please Read Carefully: Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.
- Employee Status: Regular
- Relocation: Domestic
- VISA Sponsorship: No
- Travel Requirements: 25%
- Flexible Work Arrangements: Hybrid
- Shift: 1st - Day
- Valid Driving License: No
- Hazardous Material(s): N/A
- Job Posting End Date: 10/12/2026
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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