Project Manager III

VIVOS Professional Services, LLC

Walkersville (MD)

On-site

USD 82,656 - 89,544

Full time

14 days+

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Job summary

VIVOS Professional Services, LLC is seeking an experienced Project Manager III / Product Manager in Walkersville, MD. This role focuses on managing product lifecycles in the bioprocessing sector, emphasizing cell & gene therapy solutions. The ideal candidate will have significant experience in product management and regulatory processes, alongside strong communication and analytical abilities. This position is crucial for aligning cross-functional teams to drive innovation and growth in global markets.

Qualifications

  • Experience in Product Management within Biotech or Life Sciences.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Strong analytical, communication, and stakeholder management skills.

Responsibilities

  • Lead lifecycle management and innovation strategy for the bioprocessing product portfolio.
  • Conduct market and competitive analysis to identify growth opportunities.
  • Collaborate with marketing teams to develop global marketing plans.

Skills

Product Management
Project Management
Cross-functional collaboration
Analytical skills
Stakeholder management

Job description

Pay Rate: $60–65/hr on W2

Position Overview

We are seeking an experienced Project Manager III / Product Manager – Bioprocessing CGT to drive business growth through proactive product lifecycle management, innovation strategy, portfolio expansion, and cross-functional collaboration.

This role serves as the central interface between R&D, Sales, Strategy, Marketing, Operations, and Quality teams to develop and execute global portfolio strategies for Cell & Gene Therapy (CGT) bioprocessing solutions.

The ideal candidate will have strong experience in product management, bioprocessing, life sciences, or cell & gene therapy environments, along with the ability to manage complex product portfolios, forecasting, commercialization activities, and regulatory coordination.

Key Responsibilities
  • Lead lifecycle management and innovation strategy for assigned bioprocessing product portfolio
  • Stage-gate process ownership
  • Product specifications
  • Beta testing programs
  • Product launch readiness
  • Conduct market, customer, and competitive analysis to identify unmet market needs and growth opportunities
  • Develop and manage pricing strategies across global markets
  • Partner with sales, marketing, and strategy teams to execute positioning and channel strategies
  • Identify opportunities for product improvement, margin expansion, and new technology offerings
  • Lead forecasting and inventory planning activities
  • Align production planning with sales forecasts and market demand
  • Revenue
  • Margin
  • Provide regular business performance reports to leadership
  • Support prioritization and supply planning during demand fluctuations
Marketing Support
  • Collaborate with marketing teams to develop global marketing plans
  • Support campaign development and product positioning initiatives
  • Provide technical input for marketing collateral, PR content, and product messaging
Product Sales & Technical Support
  • Serve as a technical and business subject matter expert for assigned products
  • Support customer-facing teams through:
  • Technical training
  • Regulatory support
  • Respond to non-routine technical, regulatory, and business inquiries
  • Participate in regional and global sales meetings
Safety & Regulatory Compliance
  • Support compliance activities related to:
  • FDA
  • ISO 9001:2015
  • CAPA
  • Change Control
  • Participate in Deviation Review Board meetings
  • Coordinate with Quality, Sales, and Marketing teams on customer communications and regulatory positioning
Required Qualifications
  • Experience in Product Management, Project Management, or Portfolio Management within:
  • Bioprocessing
  • Cell & Gene Therapy
  • Biotech
  • Life Sciences
  • Pharmaceutical industries
  • Strong understanding of:
  • Forecasting and inventory planning
  • Regulatory and quality processes
  • Experience collaborating with cross-functional global teams
  • Strong analytical, communication, and stakeholder management skills
  • Ability to manage multiple priorities in a fast-paced environment
Preferred Experience
  • Experience in Cell & Gene Therapy (CGT) products or GMP bioprocessing solutions
  • Knowledge of FDA and ISO regulatory requirements
  • Experience supporting product launches and commercialization strategies
  • Exposure to CAPA, Change Control, and quality systems
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