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  • Associate Director, DSCS Digital Implementation…

    Merck (Rahway, NJ)



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    Job Description

    Position Description:

    Associate Director, DSCS Digital Implementation Project Manager

     

    Within the Development Sciences and Clinical Supply (DSCS) organization, the Digital Project Manager will streamline the execution of our Company’s DSCS Digital Strategy to enable a seamless data infrastructure that drives increased speed, capacity and robustness across organizational deliverables. In this role, the DSCS Digital Project Manager will provide tactical direction and partner with the DSCS Digital Leadership Team to drive the execution and management of DSCS Digital initiatives.

     

    Development Sciences and Clinical Supply (DSCS) enables Drug Substance, Drug Product, Analytical Development, and Clinical Supply across all modalities. We are interdependent across our functional areas, Discovery, our Manufacturing Division Quality, and BARDS, to name a few, and with our partners in Finance, HR, IT, and Procurement. Together, we advance scientific and operational excellence at the interfaces of disciplines to translate breakthroughs into important new medicines and vaccines. This has a direct connection to our Company mission, and it will remain our True North. This acceleration will be supported by a foundation and a commitment to innovation and to our people. As a team, we commit to creating a culture of diversity, equity and inclusion so everyone can bring their whole self to work.

     

    We are seeking a seasoned Project Manager with a strong background in the biotech industry to lead digital transformation initiatives. This role will focus on helping the team build and manage digital tools that enhance operational efficiency and data-driven decision-making. Under the broad guidance of the DSCS Digital Program Mgmt Lead, the Associate Director, DSCS Digital Project Manager, will be responsible for implementing improved project management methodologies across DSCS Digital use-cases. The ideal candidate should have strong project management and stakeholder management skills and a demonstrated commitment to operational excellence, with an established track record in solving complex problems. Experience in one or more of the areas of Drug Substance development, Drug Product development, Clinical Supply management or Analytical Research is critical for understanding business opportunities, outcomes and execution. A passion for the value that digital solutions can bring to our operations is desirable.

    The responsibilities of the include:

    + **Project Management** : help develop and maintain a comprehensive implementation plan for each use-case, inclusive of timelines, milestones, and resources on portfolio management tool. Ensures appropriate prioritization of critical tasks and manage critical path in each use case and workstream.

    + **Stakeholder Management & Communication** : in partnership with subteam and workstream leads, identifies and engages key cross-functional partners and stakeholders across functions to ensure execution meets the needs of the business. Facilitates regular use-case team meetings and workshops with Subteam-leads as needed. Create views and communication materials (PPT, Mural, etc) to help team demonstrate value and progress.

    + **Metrics management and Rollup** : Work with sub-team and use-case leads to track use-case metrics and rollup into program KPIs. Implement and manage any associated measurement methodologies (surveys, forms, etc).

    + **Budget Mgmt** : in partnership with subteam leads, usecase leads, and finance partners, helps manage use case budgets and forecasts. Support roll up reporting and preparing for budget cycles.

    + **Resource Management** : in partnership with workstream and subteam leads, helps maintain resource planning data and escalates resource needs and changes.

    + **Implementation Oversight** : helps ensure the on-time execution of all deliverables associated with each use-case implementation plan

    + **Risk Management & Issue Resolution** : proactively identifies and interrogates risks and develops appropriate mitigation strategies to ensure successful implementation of project plans. Escalates issues through the risk log and drives problem-solving and resolution within the team.

    + **Operating Model Improvement** : contribute to the development and improvement of standard work, knowledge management playbooks, and project management tools and dashboards to support deployment of digital solutions across the network. Incorporate relevant digital tools to automate and improve project/program management efficiency where relevant.

    + **Cross-Functional Team Leadership** : in partnership with Subteam-leads, helps the cross-functional use-case team to ensure successful implementation of digital solutions. Fosters a learning and collaborative team environment.

    Required Skills and Experience:

    + Experience in drug development or manufacturing, including process or analytical development, characterization, technology transfer, validation/PPQ, commercial manufacturing, and process and plant modeling.

    + General understanding of data sources and IT systems (e.g., Signals, Analytical Instrument data, Spotfire, Thoughtspot, data lakes, dashboards, data models, etc.).

    + Proficiency in portfolio management software such as Planisware, MS Planner/Dynamics 365, etc. Understanding of emerging technologies and digital tools that can be applied to project management (agentic AI, LLMs, etc)

    + Demonstrated ability to create and analyze detailed, cross-functional project plans (including interdependencies) and manage execution against those plans with disciplined urgency. Drives accountability within teams to follow through on commitments.

    + Effective team facilitation, interpersonal, and leadership skills, with the ability to establish and maintain inclusive team environments while driving scope and timeline adherence.

    + Strong collaboration, critical thinking, and problem-solving skills. Ability to resolve conflict and drive ownership and accountability.

    + Highly organized and able to drive successful prioritization exercises and change management.

    + Excellent oral and written communication skills, with demonstrated ability to tailor communications for diverse audiences. Active listener who consistently strives to understand others’ perspectives, concerns, and ideas.

    Preferred Experience and Skills

    + Process development and/or process characterization experience/deep understanding in drug substance and drug product in biotech or pharma across small and large molecules is preferred

    Education Minimum Requirement:

    + B.S. in biology, chemistry, engineering, or related field with a minimum of 8 years of experience in the biotech or pharmaceutical industry; or M.S. in biology, chemistry, engineering, or related field with a minimum of 6 years of experience in the pharmaceutical industry; or Ph.D. in biology, chemistry, engineering, or related field with a minimum of 5 years of experience in the pharmaceutical industry.

     

    Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)

     

    Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)

    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 (https://survey.sogosurvey.com/r/aCdfqL) 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 (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf)

     

    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 (https://www.msdprivacy.com/us/en/CCPA-notice/)

     
     

    Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

     

    The salary range for this role is

     

    $126,500.00 - $199,100.00

     

    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:

    VISA Sponsorship:

    Travel Requirements:

    Flexible Work Arrangements:

    Hybrid

    Shift:

    Valid Driving License:

    Hazardous Material(s):

    Required Skills:

    Budget Development, Business, Clinical Supply Chain Management, Clinical Trial Management, Compliance Frameworks, Cross-Cultural Awareness, Decision Making, Feasibility Studies, Management Process, Managing Engineering Teams, Operational Metrics, Performance Monitoring, Project Management, Research Databases, Risk Management, Status Reporting, Team Management, Technical Problem-Solving

    Preferred Skills:

    Job Posting End Date:

    08/22/2025

     

    *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:** R357556

     


    Apply Now



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