Aseptic Lead, Operations - Dundalk

Merck Merck · Pharma · Louth County, Ireland

Merck is seeking an experienced Aseptic Lead for their Dundalk facility to strengthen sterile manufacturing standards and build long-term capability. The role involves leading environmental and media simulation programs, developing aseptic qualification processes, overseeing cleanroom compliance, managing the End-to-End Media fill program, and developing the Isolator Glove Management Program. The position requires a Bachelor's Degree in a relevant field, at least 5 years of experience in drug product and sterile manufacturing, experience with media simulations, knowledge of sterile filling processes, and prior GMP audit experience.

What you'd actually do

  1. Lead the Environmental and Media Simulation Programs within the manufacturing area.
  2. Develop and implement the Aseptic qualification process within the department.
  3. Oversee compliance enhancement projects in clean room areas.
  4. Manage the End-to-End Media fill program, including strategy, competency building, execution, and GMP Audit defense.
  5. Develop and grow the Isolator Glove Management Program at the site.

Skills

Required

  • Bachelor’s Degree or higher in Science, Engineering, or related technical discipline
  • Minimum of 5 years’ experience in Drug Product and sterile manufacturing operations
  • Experience with Media Simulations, either executing or coaching teams
  • Knowledge of sterile filling processes and equipment, particularly Grade A Isolator
  • Prior experience with GMP Audits
  • Aseptic Operations
  • Contamination Control
  • Process Simulation
  • Sterile Manufacturing

Nice to have

  • Excellent communication, presentation, and interpersonal skills
  • Excellent planning and organization skills
  • Ability to align Aseptic team objectives with wider site goals and sterility assurance priorities
  • Process Improvements
  • Training Program Management
  • Decision Making

What the JD emphasized

  • Minimum of 5 years’ experience in Drug Product and sterile manufacturing operations.
  • Experience with Media Simulations, either executing or coaching teams.
  • Prior experience with GMP Audits.