Project Manager - Downstream Biologics

Validation and Engineering Group, Inc

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

Qualifications

  • Experience leading capital projects in pharmaceutical or biotechnology sectors.
  • Strong understanding of downstream biologics processes and systems.
  • Demonstrated project management through engineering and CQV phases.
  • Experience with capacity expansion in operational manufacturing facilities.
  • Proven skills in managing project scope, schedule, cost, and quality.
  • Ability to lead cross-functional teams and engage multiple stakeholders.
  • Strong communication and presentation abilities, especially with senior leadership.

Responsibilities

  • Lead capital projects from initiation to completion across all phases.
  • Manage downstream biologics processes, focusing on fill/finish and cell culture.
  • Drive initiatives for manufacturing capacity expansion.
  • Coordinate with Engineering, Site Operations, and CQV teams.
  • Present updates and key decisions to Global Engineering and executives.
  • Ensure projects meet scope, schedule, cost, and quality benchmarks.
  • Facilitate collaboration and communication throughout project lifecycles.

Benefits

  • Comprehensive health and wellness programs.
  • Opportunities for professional development and growth.
  • Flexible working arrangements.
  • Generous paid time off and holidays.
Full Job Description
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • 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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