Job Description

The Opportunity

Join a global biopharma company with a 130-year legacy and mission to achieve new milestones in healthcare. Be part of technology driven, data-led organization supporting a diversified portfolio of medicines, vaccines and animal health products. Work alongside passionate teams that use data, analytics and insights to drive decisions, and tackle some of the world’s greatest health threats.

This role is based at our Upper Gwynedd, PA or Rahway, NJ sites and follows a hybrid working model (3 days onsite, 2 days remote). Candidates are expected to reside within commuting distance of the office.

As a Director, Technical Product Management, you will own and manage the product and strategy throughout its lifecycle, ensuring it delivers business value, supports user needs, and aligns with strategic priorities. Working closely with cross-functional stakeholders, technical teams, and business partners, the role drives product vision, adoption, continuous improvement, and effective delivery while ensuring alignment with strategic goals, compliance requirements, and operational needs.

What will you do in this role

· Own product strategy and roadmap of large-scale Regulatory technical products.

· Lead global technology initiatives within Regulatory and Regulatory Information Management (RIM).

· Act as the key interface between the business stakeholders, business system owners, delivery teams and users, facilitating direct communication and stakeholder engagement.

· Define, prioritize, and manage the product backlog based on user needs, business value, and long-term sustainability.

· Drive continuous product discovery to understand user needs and translate them into solutions.

· Make product decisions aligned with strategy, value delivery, and user experience.

· Manage product metrics and performance, identifying opportunities for improvement and measuring outcomes.

· Oversee ownership of supporting technologies and tools.

· Develop and maintain documentation such as technical designs, user guides, process flows, and related support materials.

· Drive continuous improvement across financial systems, processes, and reporting capabilities.

· Ensure compliance with financial regulations, internal controls, and data governance requirements.

· Mentor and lead large scale global cross functional teams, fostering collaboration and high performance.

What Should you have

· Bachelor’s degree in information technology, Computer Science, Finance or Business

· Masters’ degree preferred.

· More than 18 years of experience directly with leading and driving Regulatory implementations and technology enabled solutions that supports Global Regulatory Affairs; including the following technologies but not limited to Veeva Vault RIM, Lorenz Docubridge, etc.

Primary skills (must-have)

· Proven experience in product management and in leading large-scale initiatives within Regulatory and Regulatory Information Management (RIM).

• Extensive experience with the specific pharmaceutical Regulatory domain.

• Direct line management experience for global teams (50+ team members).

· Ability to present effectively to global leadership teams across Research and Development for the purposes of driving results for technology solutions.

· Experience defining product KPIs, business cases, and benefit/ROI measures.

· Strong strategic thinking and problem-solving skills, with the ability to translate business needs into sustainable solutions.

· Experience in system design and technical solutioning, with the ability to align solutions to business requirements.

· Demonstrated ability to work under pressure, meet deadlines, and maintain accountability for outcomes.

· Strong track record of managing stakeholder relationships, including executive and cross-functional stakeholders in a matrix environment.

· Excellent communication and interpersonal skills, with the ability to connect technical and non-technical audiences.

· Strong analytical skills and attention to detail.

· High levels of ownership, teamwork, and organizational discipline.

· Understanding of benefits management and outcome measurement.

· Experience working in Agile environments.

· Familiarity with Jira and collaboration tools such as Confluence, Mural, and MS Teams.

· Exposure to management system development and related operational processes.

Secondary skills (nice to have)

• Experience in asset management or related data/process governance activities.

• Exposure to financial systems, reporting, or planning applications.

• Aptitude and interest in learning new technologies quickly.

• Experience working in a global environment across multiple regions or time zones.

Required Skills:

Asset Management, Backlog Management, Benefits Management, Data Governance, Internal Controls, Learning New Technologies, Management System Development, Meeting Deadlines, Process Governance, Product Backlog Management, Product Management, Requirements Management, Stakeholder Communications, Stakeholder Engagement, Stakeholder Relationship Management, Strategic Planning, Strategic Thinking, System Designs, Works Under Pressure

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

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. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement​

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$173,200.00 - $272,600.00

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 https://jobs.merck.com/us/en/compensation-and-benefits

You can apply for this role 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 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:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

07/7/2026

*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.