Merck Posted August 11, 2026

Associate Director - Value & Implementation Quality and Standards

North Wales, Pennsylvania, United States of America FULL_TIME
Medical Affairs Associate Director

Merck is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description

The Associate Director Quality and Standards (Q&S) Steward, Value & Implementation (V&I) Operations, Quality & Standards (AD, Q&S), position resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. The AD, Q&S, is a role within V&I Global Medical and Value Capabilities (V&I GMVC) that reports directly to the Director, Quality & Standards Lead. The AD, Q&S, is an integral member of the V&I Operations team serving as a subject-matter expert around Quality and Standards and is held accountable for assisting and driving execution of the V&I Operations vision. The AD, Q&S, participates in several of the following core V&I global initiatives and assumes varying degrees of project leadership:

Leading projects to create, maintain, review and train on Standards.

Working on projects collaboratively with regional leads with the goal of linking global and local Standards, performing quality and compliance functional monitoring.

Aligning V&I Standards into divisional standards (i.e., quality by design).

Aligning Standards with divisional Quality Management System (QMS).

Supports and participates in audits, as appropriate.

Incorporating into their processes the ability to create, monitor and act against risk minimization plans.

The AD, Q&S, possesses strong communication and collaboration skills and the ability to execute innovative ways of working within a complex matrix environment.

Responsibilities and Primary Activities

Leadership

Understands the mission and vision of V&I as a science-driven and patient-committed organization.

Attends V&I Operations Leadership Team and other meetings, as appropriate, as delegate for the Director, Quality & Standards Lead.

Stays current with key initiatives across V&I Operations and exhibits a high degree of collaboration with colleagues to ensure alignment across the broader organization.

Exhibits deep subject-matter expertise and strong business acumen.

Quality & Standards

Works with the Director, Quality & Standards Lead, to lead large-scale, complex projects established to create, maintain, review, and train on Standards that often involve multiple internal and external stakeholders:

Is accountable for planning, orchestrating and delivering the Standards initiatives.

Applies project charters, project plans, and risk planning to all Standards initiatives.

Manages project timelines and resources to produce results within the committed timeframe.

Collaborates with regions and countries to ensure alignment between V&I and local Standards, as appropriate.

Supports the development of Standards training and aligns with V&I Knowledge Management to execute.

Reviews Standards on a routine basis and revises Standards, process maps, forms, templates, guidelines, and supporting documentation when appropriate to ensure compliance with regulatory requirements.

Ensures periodic review of Standards per the divisional standard operating procedures (SOP) of SOPs.

Adheres to the V&I QMS continuous improvement methodology and supports efforts to maintain and improve Standards over time.

Coordinates with the Knowledge Management team and other V&I colleagues to ensure that relevant stakeholders, including new hires, obtain training on the Standards and other controlled documentation.

Develops relevant metrics associated with Standards deployment and training and puts in place the methods for collecting and disseminating those metrics.

Manages reported Quality Issues.

Provides guidance to the V&I organization on Audit Readiness.

Aligns current and planned Standards with the divisional Quality Group and V&I Compliance:

Liaises with the divisional Quality Group to ensure that V&I Standards and policies are aligned with divisional standards (i.e., quality by design) and QMS.

Monitors the impact of any business process or regulatory changes on Standards documentation.

Serves as a subject-matter expert on the impact of proposed operational changes to V&I’s ability to meet its Standards.

Serves as V&I point for Regulatory Surveillance.

Communicates the status and progress of Standards with V&I GMVC peers and engaged stakeholders.

Serves as an ambassador for Quality & Standards throughout V&I and to external stakeholders as needed:

Communicates the value and importance of Quality & Standards.

Responds to questions about Standards and the risk management that they represent to our company.

Supports audits, assessments and inspections, as well as privacy initiatives.

 

Required Qualifications, Skills and Experience

Bachelor’s degree in life sciences, business, or health care, plus five (5) years of relevant experience.

Deep understanding of the compliance requirements, environment, evolution and global nature of Medical Affairs and Outcomes Research is preferred.

Excellent interpersonal communication (written/oral) and presentation skills with ability to communicate simply and directly without ambiguity.

Must be proficient in writing clear and detailed SOPs to support standardized and efficient business operations.

Must be proficient using AI-enabled tools to simplify, author, and maintain Standards.

Understanding of Quality systems.

Strong personal integrity and high ethical standards.

Ability to organize, prioritize and work effectively in a constantly changing, ambiguous environment. Detail-oriented nature.

Experience as a member in cross-functional, global initiatives in a complex matrix.

Strong decision-making, problem-solving and analytical skills, with ability to innovate with practical solutions for complex issues.

Ability to work independently while escalating risks and issues as appropriate.

Experience working within regulations and compliance requirements.

Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint, MS Teams).

Required Skills:

Collaborative Communications, Decision Making, Detail-Oriented, Interpersonal Communication, Medical Affairs, Medical Knowledge, Outcomes Research, Project Leadership, Project Management, Project Resource Management, Standard Operating Procedure (SOP) Management

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:

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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

$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 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:

08/18/2026 *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.

Requisition ID:R409424

Job details

Seniority
Associate Director
Function
Medical Affairs
Therapeutic area
Not listed
Location
North Wales, Pennsylvania, United States of America
Employment type
FULL_TIME

How this role compares

Computed from every other active Medical Affairs role in our database, not just this employer's listings.

We currently track 260 comparable Associate Director Medical Affairs roles across 75 biopharma companies.

260Comparable roles tracked
216Currently active
75Companies hiring similar roles
33Countries represented

Salary context

49 of 260 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $156,900/yr – $247,000/yr
Lowest disclosed · Senior Medical Writer - Vaccine · Sanofi Vaccines US Inc. $122,250/yr – $176,583/yr
Peer group range $149,417 – $258,000 (median $180,500)

Where these roles are based

Top locations among the 260 comparable roles

United States88
Japan25
Germany24
India22
China20
Taiwan13

+ 27 more countries

Seniority mix

260 of 260 peers have a known seniority level

Manager125
Senior97
Associate Director38

Therapeutic area mix

101 of 260 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology43
Immunology14
Vaccines & Infectious Disease9
Cardiovascular / CVRM8
Rare Disease8
Dermatology & Aesthetics8
Neuroscience7
Respiratory2
Ophthalmology1
Gastroenterology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly Boston, Massachusetts, United States of America Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Gilead Sciences, Inc. Foster City, United States Associate Director
Same function Same seniority Same country
60%similar
Regeneron Pharmaceuticals, Inc (USA) Remote, United States Associate Director
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Director-Medical Writer
Lilly · Boston, Massachusetts, United States of America · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Medical Digital Strategy & Activation
Gilead Sciences, Inc. · Foster City, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Health Economics & Outcomes Research, Solid Tumors
Regeneron Pharmaceuticals, Inc (USA) · Sleepy Hollow, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, US Medical Learning, Neuroscience
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.