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PCI Pharma Services

Pharmaceutical packaging and contract services

Project Manager-NPI

Project ManagementConfirmed live in the last 24 hours
Full-timePhiladelphia, PA, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a technical, engineering, or science discipline is required.
  • At least 4 years of experience in pharmaceutical project management, preferably within a contract development and manufacturing organization or contract manufacturing environment.
  • Sound working knowledge of current Good Manufacturing Practice (cGMP) and Food and Drug Administration (FDA) regulatory requirements.
  • Experience managing technical projects, including integrated timeline management, risk identification, escalation, and resolution.
  • Proficiency with Smartsheet or equivalent project management platforms, and Microsoft 365 suite.
  • Ability to interact effectively with internal cross-functional teams and external clients.
  • Ability to manage multiple concurrent projects with competing priorities and deadlines.
  • Strong problem-solving skills with an analytical, detail-oriented approach.
  • Ability to influence and drive accountability across cross-functional teams without direct authority.
  • Dependability, reliability, integrity, and attention to detail.
  • Customer-centric mindset with a commitment to quality, ethics, and professionalism.

Responsibilities

  • Own end-to-end project-level execution of assigned new product introduction (NPI) programs from award through commercialization, managing integrated project timelines, milestones, dependencies, and deliverables.
  • Maintain project plans, action trackers, and RAID logs in Smartsheet; track progress against milestones and escalate schedule, cost, or scope risks to the Program Manager early.
  • Prepare and deliver weekly project status updates for internal governance and leadership reporting, keeping documentation, templates, and systems including Smartsheet and JDE accurate and current.
  • Ensure project activities follow the NPI Playbook and standard ways of working established by the NPI function.
  • Ensure activities comply with cGMP, FDA 21 CFR 211, applicable regulatory standards, PCI standard operating procedures (SOPs), and environmental, health, and safety (EHS) requirements.
  • Drive cross-functional coordination across Engineering, Quality Assurance, Quality Engineering, Operations, Procurement, Supply Chain, and Validation to keep project deliverables on track.
  • Lead weekly internal project team meetings and ensure clear accountability for action items across functional areas.
  • Align Engineering, QA, Operations, and Supply Chain on technical requirements, material readiness, and validation plans; ensure procurement timelines and material availability align with project milestones.
  • Serve as the primary day-to-day operational contact for assigned clients during active project execution, escalating strategic or relationship-level issues to the Program Manager.
  • Lead or co-lead client steering committee meetings for assigned programs, preparing agendas, status materials, and action-item tracking in coordination with the Program Manager.
  • Provide internal and external project status reporting, including schedule adherence, risk and issue summaries, and budget status as required.
  • Drive projects through formal NPI stage gates (Kickoff, Development, Tech Transfer, Validation, and Commercialization), ensuring gate deliverables are completed before phase transitions.
  • Partner with the Project Engineering team throughout the NPI lifecycle to align on equipment readiness, technical requirements, process development activities, and validation execution; support the team with scheduling coordination, client communication, and cross-functional issue resolution.
  • Coordinate technology transfer, engineering runs, operational qualification (OQ), process line trials (PLT), process qualification (PQ/PPQ), and launch readiness activities, including in-person walkthroughs and alignment sessions on the manufacturing floor.
  • Ensure floor readiness and Business Unit resource availability before key manufacturing phases; confirm batch records, Master Packaging Instructions (MPIs), specifications, and quality approvals are in place before validation runs.
  • Track readiness of components, tooling, and materials; coordinate with Procurement and Supply Chain to resolve shortages or lead-time issues and ensure items arrive in time for engineering and validation runs.
  • Ensure program timelines account for regulatory submissions, approvals, and inspection-readiness milestones.
  • Monitor project scope against awarded work and identify potential scope changes, escalating them to the Program Manager with supporting documentation for financial review.
  • Track key program cost drivers that could affect timelines, budgets, or capacity planning and report variances to the Program Manager.
  • Support timely submission of Capital Expenditure Requests (CERs) related to NPI programs and assist with onboarding cost tracking as directed by the Program Manager.
  • Maintain a working relationship with Business Development to support the BD-to-NPI handover, ensuring project-level technical requirements, commercial terms, and timeline expectations are accurately captured and incorporated into project plans.
  • Coordinate product destruction after validation runs, ensuring proper documentation, client approvals, and compliance with PCI procedures and regulatory requirements.
  • Capture lessons learned throughout the project lifecycle and contribute to improving the NPI Playbook, templates, and processes.
  • Provide the Program Manager with feedback on process gaps, operational challenges, and improvement opportunities identified during project execution.
  • Coordinate with internal change-control processes to manage changes affecting project scope or timelines, ensuring proper documentation and approvals.
  • Adhere to standard operating procedures, health and safety requirements, cGMP, and regulatory guidelines.
  • Escalate project-level risks, scope changes, and issues to the Program Manager for resolution or further escalation.
  • Travel occasionally for vendor, supplier, or client engagements.

Desired Qualifications

  • A master's degree in a technical, engineering, or science discipline.
  • PMP, PRINCE2, or equivalent project management certification.
  • Experience with technology transfer, process validation (PLT/PQ/PPQ), or commercial manufacturing readiness activities.
  • Understanding of drug product manufacturing processes, equipment, and packaging operations.
  • Experience working directly with pharmaceutical clients as the primary operational point of contact.
  • Familiarity with stage-gate or phase-gated project management methodologies in a GMP manufacturing environment.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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