Associate Specialist, Operations

Merck Merck · Pharma · NC

Associate Specialist, Operations role at Merck focused on continuous improvement for a capital project start-up in a pharmaceutical manufacturing facility. Responsibilities include supporting project design, development, delivery, and evaluation, managing project schedules and dashboards, analyzing initiatives for success, and partnering with leadership on Lean Methodology implementation. Requires strong analytical, problem-solving, collaboration, and communication skills. Experience with project management and GMP manufacturing is preferred.

What you'd actually do

  1. Working within the Operations management team to create and execute strategies that support design, development, delivery and evaluation of projects related to steady-state production and/or continual process improvement.
  2. Ensuring visibility and accuracy of the project schedule and update dashboards accordingly to highlight the project status of critical milestones.
  3. Analyzing and implementing initiatives that will help to increase overall success within the department.
  4. Effectively using metrics and measurement to ensure that projects and initiatives result in desired outcomes.
  5. Ability to prioritize workload under guidance from management.

Skills

Required

  • Analytical Problem Solving
  • Business Operations
  • Change Management
  • Communication
  • Conflict Resolution
  • Critical Thinking
  • Fast-Paced Environments
  • GMP Compliance
  • Good Manufacturing Practices (GMP)
  • Internal Customers
  • Machinery Operation
  • Manufacturing Operations
  • Process Optimization
  • Production Planning
  • Production Scheduling
  • Project Controls
  • Project Facilitation
  • Project Management
  • Raw Material Specifications
  • Regulatory Compliance
  • Teamwork
  • Technical Problem-Solving

Nice to have

  • Lean Six-Sigma methodologies
  • shop-floor cGMP manufacturing and related systems (i.e. SAP)
  • pharmaceutical regulatory requirements
  • Project management and data analysis skills
  • Technical writing experience
  • facility, equipment and/or process start up activities in a cGMP environment
  • Demonstrated ability to work independently