Project Manager - Downstream Biologics

Validation and Engineering Group, Inc

$90K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Experience leading capital projects in the pharmaceutical or biotechnology sectors.
  • In-depth knowledge of downstream biologics manufacturing processes.
  • Proven track record managing projects through CQV phases.
  • Background in capacity expansion within production facilities.
  • Strong project management skills to oversee scope, schedule, and quality.
  • Experience in leading and coordinating cross-functional teams.
  • Excellent communication and presentation abilities.

Responsibilities

  • Lead projects from initiation to CQV completion.
  • Manage downstream biologics processes like fill/finish and cell culture.
  • Drive capacity expansion initiatives in existing facilities.
  • Coordinate efforts across Engineering, Operations, and CQV teams.
  • Present updates and decisions to leadership and executives.
  • Ensure projects meet scope, schedule, and quality standards.
  • Facilitate collaboration and communication across stakeholders.

Benefits

  • Opportunities for professional development and growth.
  • Collaborative work environment with cross-functional teams.
  • Access to advanced technology and manufacturing practices.
  • Potential for project leadership experience in a growing field.
Full Job Description
  • Project Manager - Downstream Biologics

Description:

Leads capital projects within downstream biologics manufacturing, supporting capacity expansion and facility enhancements within existing operations. Manages projects through the full project lifecycle from concept through engineering, construction, and CQV, ensuring alignment with business and site objectives.

Responsibilities:
  • Lead capital projects from initiation through design, construction, and CQV completion.
  • Manage projects related to downstream biologics processes, including fill/finish, cell culture, reactors, and related systems.
  • Drive capacity expansion initiatives within existing manufacturing facilities.
  • Coordinate cross-functional teams including Engineering, Site Operations, and CQV stakeholders.
  • Present project updates, project status, and key decisions to Global Engineering leadership and site executives.
  • Ensure adherence to scope, schedule, cost, and quality objectives.
  • Manage project execution to support business goals and site operational requirements.
  • Facilitate communication and collaboration across project teams and stakeholders.
  • Support project planning, risk management, and decision-making throughout the project lifecycle.


Qualifications:
  • Experience leading capital projects within pharmaceutical, biotechnology, or biologics manufacturing environments.
  • Strong knowledge of downstream biologics manufacturing processes, including fill/finish, cell culture, reactors, and associated process systems.
  • Experience managing projects through engineering, construction, commissioning, qualification, and validation (CQV) phases.
  • Experience supporting manufacturing capacity expansion projects within existing operating facilities.
  • Strong project management skills with demonstrated ability to manage scope, schedule, cost, and quality objectives.
  • Experience leading cross-functional teams and coordinating multiple stakeholders.
  • Strong leadership, communication, and presentation skills.
  • Ability to present project updates and strategic recommendations to senior leadership and executive stakeholders.
  • Strong organizational, analytical, and problem-solving skills.
  • Ability to manage multiple priorities in a fast-paced project environment.
  • Available to work extended hours, possibility of weekends and holidays.

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