Aseptic Lead, Operations - Dundalk

MSD; Leinster; Hybrid; EUR 95,000 - 135,000; Full time

Job summary

MSD is seeking an experienced Aseptic expert to strengthen sterile manufacturing standards and build long-term capability. You will shape how aseptic practices are applied, improved, and sustained across the site, preparing the facility for commercial sterile production with robust processes and qualified personnel.

You will lead environmental and media simulation programs, develop aseptic qualification, and drive contamination control while ensuring compliance with cGMP and regulatory

Qualifications

• Adaptability and teamwork in a fast-paced manufacturing environment.
• Strong understanding of aseptic processing and sterile filling operations.
• Experience with GMP audits and contamination control.
• Ability to plan, coordinate, and lead training and qualification programs.

Responsibilities

• Lead Environmental and Media Simulation Programs within the manufacturing area.
• Develop and implement the Aseptic qualification process within the department.
• Oversee compliance improvement projects in clean room areas.
• Manage End-to-End Media fill program, including strategy, competency building, execution, and GMP Audit defense.
• Develop and grow the Isolator Glove Management Program at the site.
• Contribute to cleanroom operations and contamination control procedures, including cleaning, sanitization, garbing, and segregation.
• Ensure compliance with company policies, procedures, guidelines, and regulatory requirements, executing cGMP in daily activities.
• Provide SME insight during deviations or audit activities and serve as the manufacturing IPT lead in Sterile Council and Sterile CoP.

Skills

Adaptability

Aseptic Operations

Contamination Control

Decision Making

Process Improvements

Sterile Manufacturing

Training Program Management

Education

Bachelor’s Degree or higher in Science/Engineering/related technical discipline

Job description

Job Description

Position Overview

We’re looking for an experienced Aseptic expert who enjoys working hands-on with teams to strengthen sterile manufacturing standards and build long-term capability. You’ll be a trusted subject matter expert, shaping how aseptic practices are applied, improved, and sustained across the site.

The role is instrumental in preparing the site for commercial sterile manufacturing by ensuring robust aseptic processes, qualified personnel, effective contamination control measures, and inspection-ready systems that support long-term operational success.

Responsibilities

• Lead the Environmental and Media Simulation Programs within the manufacturing area.
• Develop and implement the Aseptic qualification process within the department.
• Oversee compliance enhancement projects in clean room areas.
• Manage the End-to-End Media fill program, including strategy, competency building, execution, and GMP Audit defense.
• Develop and grow the Isolator Glove Management Program at the site.
• Contribute to cleanroom operations and contamination control procedures, including cleaning, sanitization, garbing, and segregation.
• Ensure compliance with our company’s global policies, procedures, guidelines, and regulatory requirements, executing cGMP in daily activities.
• Provide SME insight during deviations or audit activities and serve as the manufacturing IPT lead in Sterile Council and Sterile CoP.

Qualifications 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. Preferred
• Excellent communication, presentation, and interpersonal skills to interface effectively with all levels of colleagues and external customers in a team-oriented manner.
• Excellent planning and organization skills to manage training programs, assessments, and cleanroom support.
• Ability to align Aseptic team objectives with wider site goals and sterility assurance priorities.

Required Skills

Adaptability, Aseptic Operations, Contamination Control, Decision Making, Process Improvements, Sterile Manufacturing, Training Program Management

Secondary Language(s) Job Description

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.

Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.

Please feel free to speak to us about what flexibility means to you during your application.

Employee Status

Regular

Flexible Work Arrangements

Not Applicable

Job Posting End Date

08/31/2026

• A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID

R412014