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Senior Specialist, Project Management – Chemistry Manufacturing & Controls

Job in Paterson, Passaic County, New Jersey, 07544, USA
Listing for: Jobtailor
Full Time position
Listed on 2026-08-02
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

Responsibilities

  • Manage the end‑to‑end development process for moderate complexity projects and work with CIPM team members to ensure successful execution of more complex strategies and project plans, guiding teams to develop comprehensive strategies and ensure successful execution.
  • Guide teams through the creation, approval, and execution of integrated project plans appropriate to the project's phase of development and complexity.
  • Build and maintain project schedules and critical project information, using these tools to integrate activities across key functional areas, work with team leads to proactively identify risks, and ensure clear and effective communication with key team, management, and cross‑departmental stakeholders.
  • Leverage relationships and networks to improve and enhance team dynamics, with guidance from senior CIPM team members and team leads as needed, to proactively identify and remove obstacles to drive business results.
  • Navigate our company's process and organizational norms to enable teams to understand corporate governance and business requirements, thereby enabling informed decision‑making.
  • Prepare for and facilitate key team meetings including creating thoughtful agendas, ensuring appropriate participation, contributing project management insights, and following up to ensure the team continues to make progress while holding others accountable.
  • Participate in CIPM and GPAM departmental initiatives and work streams aimed at improving the way that we work and the way that we interact with one another as well as other departments.
Requirements
  • Bachelor’s degree required; concentration in a scientific or applied discipline preferred.
  • Minimum of three (3) years of experience in project management or a related role required.
  • Experience with the planning and execution of strategies for drug/vaccine product registration and commercialization/life‑cycle management (can be R&D, manufacturing, or commercial perspective).
  • Demonstrated ability to work independently to effectively accomplish goals in a team setting.
  • Demonstrated ability to serve as a resource for colleagues and program teams.
  • Effective interpersonal skills and ability to work collaboratively across diverse teams and networks; able to foster cooperation in others.
  • Highly organized and capable of working with attention to detail; excellent problem‑solving skills and ability to build alignment around complex situations.
  • Strong communication skills, both oral and written.
  • Knows when and how to speak up and appropriately raise issues to team and to management.
  • Ability to succeed in a dynamic environment with flexibility to respond to changing priorities.
Certifications & Qualifications
  • Bachelor's degree.
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Position Requirements
10+ Years work experience
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