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Alcami

Pharmaceutical and biologics CDMO services

Project Manager 2 - Multiple Teams

Project ManagementPosted on Nov 11
Full-timeMorrisville, NC, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific discipline is required; a master's degree is preferred.
  • Three years of related pharmaceutical or biotechnology experience are required.
  • Two years of experience leading multidisciplinary project teams in a service business are required.
  • Three to five or more years of project management experience are required.
  • Prior experience in a customer-facing role is required.
  • The candidate must have technical and scientific knowledge of Alcami services within the customer's project and contract.
  • The candidate must understand a product lifecycle through regulatory phases from pre-clinical development to commercialization and identify activities needed for regulatory approval.
  • The candidate must have technical and scientific aptitude to lead a Drug Product project team and set timelines and milestones.
  • The candidate must be able to communicate technical details to internal stakeholders and customers, including highly educated industry thought leaders.
  • The candidate must be able to organize and run business and project review meetings with a joint steering committee, answer impromptu questions, and provide real-time updates.
  • The candidate must be able to resolve conflicts between company and customer timelines by influencing the project team or advocating for the company's position.
  • The candidate must know multiple validated GMP systems and understand contracts and financial impacts.
  • The candidate must be able to maintain multiple files across a variety of systems and manage competing technical and business priorities.
  • The candidate must have verbal, written, and presentation skills.
  • The candidate must be able to motivate and influence others and facilitate subject-matter experts associated with projects.
  • The candidate must be proficient with computer systems, including Microsoft Office, Smartsheet, and Salesforce.
  • The candidate must have experience identifying risks related to drug development, timelines, budgets, and compliance.
  • The candidate must have experience applying risk management through Failure Mode and Effects Analysis (FMEA).
  • The candidate must be able to identify workflow-streamlining processes, anticipate factors that could affect projects, and develop contingency plans.
  • The employee must meet the stated physical demands, including lifting up to 50 pounds occasionally, and use required personal protective equipment in lab or manufacturing areas.

Responsibilities

  • Establish, lead, and manage technical and scientific project teams to deliver Alcami services according to contracted commitments and timelines.
  • Assess contract scope and create detailed timelines of actions, deliverables, and risks.
  • Identify and request technical and scientific resources from functional areas, including operations, formulation development, analytical development, quality, and engineering.
  • Review contract scope and project schedules with the project team to identify gaps, risks, and additional services needed for successful execution.
  • Communicate out-of-scope items that may require contract amendments to Business Development.
  • Lead customer project kick-off meetings, introducing the team and presenting scope, timelines, risks, and proposed additional activities.
  • Lead project activities, monitor progress against timelines, update internal stakeholders and customers, and use technical and scientific knowledge to manage activities at risk of exceeding timeframes or contract scope.
  • Escalate project or customer relationship issues to internal stakeholders, propose corrective actions, and manage customer responses and action plans to resolve conflicts.
  • Maintain accurate timelines, monitor forecasted revenue, and track and manage GMP documentation through Master Control, the validated electronic document management system.
  • Update site files used to calculate and display project metrics, including Right First Time, On Time Delivery, and Schedule Adherence.
  • Monitor, forecast, and calculate assigned project profitability.
  • Generate change orders and work with Business Development to prepare proposals for additional project work.
  • Serve as the customer's primary contact for project activities and issues, including invoice questions or disputes.
  • Partner with the Director of Project Management to improve project management processes and systems.
  • Ensure timely completion of and compliance with cGMP and other required company training.
  • Travel to manufacturing locations to host clients and conduct site visits.
  • Perform other duties as assigned.

Desired Qualifications

  • CMO or CDMO experience is preferred.
  • Formal project management training or certification is preferred.
  • PMP certification is desired.

About the Company

Alcami

Pharmaceutical and biologics CDMO services

Alcami is a contract development and manufacturing organization supporting pharmaceutical and biologics companies from early development through commercial production. Services span drug product manufacturing (sterile fill-finish and oral solid dose), analytical and microbiology lab testing, and cGMP storage with validation and environmental monitoring. What sets Alcami apart is its integrated, end-to-end capabilities across the development lifecycle. The goal is to help pharma and biotech partners deliver safe, high-quality therapies to patients.

Company size
51-200
Company stage
Not listed
Total funding
Not listed
Headquarters
Pepperell, MA
Founded
1984

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