Job Description
Global Quality Program Integration Manager
Join our manufacturing division as a Global Quality Program Integration Manager and play a pivotal role in managing critical Global Quality Laboratory Transformation Initiatives, activities, and budgets. This is an exciting opportunity to work in a fast-paced, matrixed organization and make a significant impact on our mission to save and improve lives around the world.
Responsibilities
Work closely with key internal and external stakeholders across various cross-functional groups at a regional and global level.
Integrate numerous complex and aggressive workstream plans across multiple functions and external entities.
Resolve conflicts and make trade-offs between competing interests and priorities to ensure the overall success of the project.
Facilitate key joint meetings together with alliance counterparts.
Ensure streamlined and efficient communication, including scheduling touchpoint-based communications with key stakeholders and participating in cross-function execution and governance meetings.
Work closely with accountable groups to ensure budget accountability and transparency with stakeholders and governance.
Track activity timing, anticipated risk, and mitigation of issues/conflict resolutions with alliance counterparts as well as internal stakeholders.
Lead and contribute to process-improvement initiatives.
Encourage overall operational excellence across all activities and projects.
Assist with the planning, orchestrating, and support of business initiatives.
Support projects that often involve multiple internal and external stakeholders, including budget planning, meeting planning, and agenda/meeting minutes.
Track and support multiple work-streams across multiple functional areas and multiple companies.
Lead Microsoft Teams community stewardship.
Support and execute communication plans that align to business objectives and project timelines and meet stakeholder needs.
Interact with leadership to understand business goals and performance needs, develop and execute ways of working that align with our company's business strategy, and routinely engage with key stakeholders to ensure solutions continue to support and positively drive desired outcomes.
Qualifications
Required
Bachelor's degree
- A minimum of eight (8) years of experience in the Pharmaceutical Manufacturing / Quality Environment (understanding regulatory compliance, FDA/EMA inspection readiness, LIMS/ELN systems, and lab instrumentation)
- A minimum of five (5) years of project-management experience
- Experience with the planning, logistics, and facilitation of executive-level meetings internally and externally.
- Strong interpersonal, verbal, and written communication skills to work with regulatory, quality, capital, and/or scientific teams.
- Strong ability to influence and negotiate among teams and individuals with competing priorities and quickly guide teams to solutions in the best interest of the overall project.
- Ability to independently handle multiple projects and priorities simultaneously and function in a fast-paced environment.
- Experience working effectively both independently and as part of a team.
- Ability to quickly and comprehensively learn about new subject areas and environments.
- Self-motivation, flexibility, resourcefulness, ability to problem solve, and a passion for science.
- Outstanding Microsoft Word, PowerPoint, Excel, and Teams skills.
- Demonstrated ability to apply approaches, tools, and techniques for working with peers and groups in a constructive and collaborative manner.
- Ability to express oneself to provide information to others effectively and in a succinct manner; advanced verbal, written, and presentation abilities; ability to ask thoughtful questions to gain insights, listen, and understand other perspectives.
- Ability to use a broad range of methods, assumptions, frameworks, and perspectives when solving problems and making decisions.
- Tactical and strategic project-planning and project-management experience, including the ability to contribute to operational (short term), tactical (one to two years), and strategic (three to five years) planning in support of the business plan.
- Willingness to promote team collaboration and effectiveness across country and regions.
Preferred
Alliance project-management experience.
Prior experience leading large, complex multi-stakeholder projects.
Prior vendor-management and budget-planning experience.
Required Skills:
Ability to Coordinate, Ability to Coordinate, Business Decisions, Change Management, Client Project Management, Communication Management, Construction Site Management, Cross-Cultural Awareness, Enterprise Leadership, Executive Leadership, Facilities Development, Influencing Skills, Meeting Facilitation, Mentoring Staff, Negotiation, Pharmaceutical Projects, Pharmaceutical Quality Assurance, Presentation Delivery, Project Construction Management, Project Development, Project Management, Project Management Methodology (PMM), Project Management Principles, Project Planning, Project Schedule Development {+ 7 more}
Preferred Skills:
Current Employees apply
Current Contingent Workers apply
US and Puerto Rico Residents Only:
The salary range for this role is
$156,900.00 - $247,000.00
This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include 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 .
You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
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:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
09/26/2026
*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.
