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Merck Associate Director Jobs in Summit, NJ (NOW HIRING)

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Merck Associate Director information

See Summit, NJ salary details

$32.4K

$109.2K

$183.8K

How much do merck associate director jobs pay per year?

As of Aug 11, 2026, the average yearly pay for merck associate director in Summit, NJ is $109,158.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,400.00 and $149,800.00 per year, depending on experience, location, and employer.

What is the difference between Merck Associate Director vs Merck Senior Manager?

CriteriaMerck Associate DirectorMerck Senior Manager
Required credentialsAdvanced degree (MBA, PhD), relevant industry experienceBachelor's or Master's degree, significant industry experience
Work environmentStrategic leadership, cross-functional collaborationOperational management, team oversight
Employer and industry usageCommon in pharmaceutical and biotech sectorsWidely used in similar sectors for mid-to-senior roles
Search and comparison intentHigh overlap in responsibilities and qualificationsSimilar level, often compared for career progression

The Merck Associate Director typically holds a more strategic, leadership-focused role requiring advanced degrees and extensive industry experience. In contrast, the Merck Senior Manager is more operational, overseeing teams and projects. Both roles are integral in pharmaceutical companies, with the Associate Director often preparing for executive leadership, while the Senior Manager manages day-to-day functions.

What does a Merck Associate Director do?

A Merck Associate Director typically oversees teams or projects within a specific department, such as research, marketing, or regulatory affairs. They are responsible for developing strategies, ensuring compliance with company and regulatory standards, and achieving departmental goals. Associate Directors often manage budgets, mentor staff, and collaborate with other leaders to drive business objectives. Their role is critical in advancing Merck’s mission and maintaining high performance across their area of responsibility.

What are some common challenges faced by a Merck Associate Director, and how can candidates prepare to address them?

As an Associate Director at Merck, one common challenge is balancing strategic leadership with hands-on project management, especially in a fast-paced, highly regulated environment. You'll often need to coordinate cross-functional teams and align diverse stakeholders, so strong communication and organizational skills are key. Candidates should be prepared to navigate shifting priorities, regulatory changes, and tight deadlines while ensuring alignment with Merck’s mission and compliance standards. Proactively building knowledge in pharmaceutical regulations and stakeholder management can help you succeed in this role.

What are the key skills and qualifications needed to thrive as a Merck Associate Director?

To thrive as a Merck Associate Director, you typically need a relevant advanced degree (such as in life sciences, business, or a related field), substantial industry experience, and strong leadership capabilities. Familiarity with regulatory compliance systems, data analysis tools, and project management software is often required, along with any specialized certifications pertinent to the business area. Strategic thinking, effective communication, and the ability to lead cross-functional teams are crucial soft skills in this role. These competencies are vital for driving business objectives, ensuring regulatory adherence, and fostering effective team collaboration within a complex corporate environment.
What job categories do people searching Merck Associate Director jobs in Summit, NJ look for? The top searched job categories for Merck Associate Director jobs in Summit, NJ are:
What cities near Summit, NJ are hiring for Merck Associate Director jobs? Cities near Summit, NJ with the most Merck Associate Director job openings:
Infographic showing various Merck Associate Director job openings in Summit, NJ as of August 2026, with employment types broken down into 1% As Needed, 64% Full Time, 29% Part Time, 3% Temporary, and 3% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $109,158 per year, or $52.5 per hour.

Associate Director - Value & Implementation Quality and Standards

Merck & Co.

Rahway, NJ

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job DescriptionThe 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 ActivitiesLeadershipUnderstands 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 & StandardsWorks 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 ExperienceBachelor'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) ManagementPreferred 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 $156,900.00 - $247,000.00This 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: RegularRelocation:No relocationVISA Sponsorship:No Travel Requirements: 10%Flexible Work Arrangements:HybridShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob 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 Salary: . Date posted: 08/04/2026

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