Director, Quality Assurance – Value Chain Management (Global, Hybrid)

MSD

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profile Job Location:

Dublin - Ireland

profile Monthly Salary: Not Disclosed
Posted on: 14 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Description

Were looking for a Director of Quality Assurance to lead quality across the full value chain for a latestage ophthalmic this role youll be a core member of the Value Chain Management Team guiding strategy ensuring compliance and enabling manufacturing excellence from development through commercialization. Youll partner across Quality Regulatory Technical and Supply Chain teamscoaching facilitating and removing obstacles so the program can thrive.

Bring energy knowledge innovation to carry out the following:

  • Own the products quality strategy aligned to supply strategy and ensure clear documentation and execution
  • Shape the analytical strategy (labs testing approaches stability) and support site selection
  • Provide handson quality leadership to product and focus teams; advise problemsolve and drive continuous improvement
  • Implement and oversee fitforpurpose Quality Management Systems and standard ways of working
  • Stay current on regulations and apply them pragmatically; support inspections and champion ongoing inspection readiness
  • Partner with Corporate Quality and other sites to share best practices and align on quality systems
  • Lead quality communications across the network; run meetings surface risks and escalate issues when needed
  • Track and interpret key metrics (changes complaints annual product reviews) to identify trends and mitigate risk
  • Review and approve crosssite evaluations and postmarketing assessments
  • Monitor franchise quality risks and performance with site quality teams
  • Represent Quality on the Value Chain Management Team and related working groups; lead or contribute to chartered projects

What skills you will need:

In order to excel in this role you will more than likely have:

  • 10 years in the pharmaceutical industry with proven leadership experience
  • Deep quality expertise; experience with ophthalmic or large molecules is a plus
  • Background in continuous improvement or analytics is helpful
  • Strong project management communication and stakeholder skills
  • Experience leading crossfunctional teams to deliver on strategic initiatives
  • Degree in a science pharmacy or engineering discipline; advanced degree welcome
  • Track record of driving change and measurable improvements
  • Commitment to professional growth and continuous learning
  • Collaborative mindset and ability to build trust across diverse teams

  • Travel requirement:
    • Willingness to travel 10-15% for assignments outside your primary location including short-term travel as needed

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the worlds most challenging healthcare needs.

As an equal opportunity employer we are proud to be a company that embraces the value of bringing diverse talented and committed people together. Please dont hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application.

So if you are ready to:

Invent solutions to meet unmet healthcare needs please apply today.

Required Skills:

Communication Entrepreneurship Execution Excellence Influence Leadership Networking and Partnerships Program Management Quality Management Systems (QMS) Quality Strategy Regulatory Compliance Risk Management Stakeholder Management

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/26/2025

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Director

Job DescriptionWere looking for a Director of Quality Assurance to lead quality across the full value chain for a latestage ophthalmic this role youll be a core member of the Value Chain Management Team guiding strategy ensuring compliance and enabling manufacturing excellence from development thro...
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Key Skills

  • Quality Assurance
  • FDA Regulations
  • ISO 9001
  • Root cause Analysis
  • Biotechnology
  • Clinical Trials
  • Quality Systems
  • Food Processing
  • Quality Control
  • Quality Management
  • cGMP
  • HACCP

About Company

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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