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ASSOCIATE DIRECTOR OF PROJECT MANAGEMENT

LGM Pharma

Rosenberg, TX
Full Time
Director
5 days ago

Job Description

About the Role

The Associate Director of Project Management is responsible for overseeing and leading a portfolio of complex projects and cross-functional teams to ensure successful delivery within budget and timelines. This role involves developing detailed project plans, managing stakeholder communication, and contributing to project management best practices within a pharmaceutical CDMO environment.

Key Responsibilities

  • Oversee and lead a portfolio of complex project and cross functional teams to ensuring successful delivery within budget and timelines
  • Develop detailed project plans, timelines, resource allocations, and budgets for assigned projects, ensuring alignment with business goals
  • Lead and manage cross-functional project teams, assigning tasks, providing guidance, and motivating team members to achieve project milestones
  • Effectively communicate project status, risks, and issues to key stakeholders, including senior leadership, ensuring transparency and alignment
  • Identify potential project risks, develop mitigation strategies, and proactively manage risks throughout the project lifecycle
  • Monitor project quality, ensure adherence to established standards and processes, and implement quality control measures
  • Track project budgets, identify cost variances, and take corrective action to maintain financial integrity
  • Prepare regular project reports, analyze performance metrics, and identify areas for improvement
  • Contribute to the development and implementation of project management methodologies and best practices within the organization
  • Process Quotations for new Product Cost of Goods (COGS)
  • Keep working teams on track to meet monthly billing goals
  • Perform other related duties as assigned

Requirements

  • Bachelor's Degree in the life science field, engineering or other related technical field
  • 8+ years' experience in pharmaceutical CDMO environment
  • Experience in either SOLID DOSE or SEMI-SOLID DOSE pharmaceutical product development/manufacturing required
  • Proven experience in project management, ideally with a track record of successfully managing large, complex projects across different business functions
  • Experience with or ability to rapidly understand job costing
  • Ability to understand, interpret and effectively communicate complex technical information to multiple levels inside and outside the organization
  • Excellent interpersonal skills
  • Excellent attention to detail
  • Excellent organizational and time management skills with a proven ability to meet deadlines
  • Strong analytical, problem-solving and decision-making skills
  • Adept in handling multiple tasks and challenges concurrently
  • Proficient Computer Skills (ie, MS Project, Word, Excel, PowerPoint, SalesForce, Manufacturing/Job Processing Software (ie MasterControl, SAP, etc))

Qualifications

  • Bachelor's Degree in the life science field, engineering or other related technical field
  • 8+ years' experience in pharmaceutical CDMO environment
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Job Details

Posted AtJun 17, 2025
Job CategoryProject Management
SalaryCompetitive salary
Job TypeFull Time
ExperienceDirector

About LGM Pharma

Website

lgmpharma.com

Company Size

101-250 employees

Location

Rosenberg, TX

Industry

Pharmaceutical and Medicine Manufacturing

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