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Aseptic Filling Manager
role at
Grifols
Would you like to join an international team working to improve the future of healthcare?
Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world.
We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
At Grifols, we believe that diversity adds value to our business, our teams, and our culture.
We are committed to equal employment opportunities that foster an inclusive environment.
Overview
The Aseptic Filling Manager is responsible for overseeing the daily operations of the Aseptic Filling Team, ensuring compliance with cGMP standards, safety regulations, and company policies.
This role leads the planning, organization, and execution of filling operations, ensuring optimal performance, productivity, and quality.
The manager will oversee the operation, cleaning, assembly, and maintenance of equipment such as filling lines, autoclaves, parts washers, and other aseptic processing and cleanroom equipment.
The position also requires strong leadership to develop team members, drive continuous improvement, and support regulatory readiness.
What you will be doing
Plan and organize job assignments in alignment with the production schedule, cGMP requirements, and safety regulations.
Ensure equipment is operated, cleaned, and maintained according to established procedures.
Oversee process control adjustments and maintain accurate records/logs.
People Management
Manage employee performance, development, and attendance.
Coach, mentor, and counsel team members; delegate effectively to senior staff (coordinators, senior technicians) to build capability.
Conduct annual and mid-year performance reviews.
Ensure timely, consistent, and effective training for all team members.
Promote a culture of safety, integrity, and collaboration.
Compliance & Quality
Serve as a subject matter expert for troubleshooting and maintaining optimal process parameters.
Investigate and resolve process deviations, documentation errors, and related issues.
Ensure strict adherence to cGMPs, company policies, and safety rules.
Support and facilitate regulatory inspections and audits.
Continuous Improvement & Project Support
Provide insight into resource, headcount, and raw material planning.
Contribute to budgeting activities.
Participate in or lead project initiatives such as new technology implementation or SAP enhancements.
Apply Lean and/or Six Sigma methodologies to improve processes and reduce waste.
Education & Experience
Bachelor's degree in a related field.
Minimum 5 years' experience in pharmaceutical, bioscience, or medical device manufacturing.
Minimum 5 years' management experience leading a team of 10 or more.
Lean or Six Sigma certification preferred.
Technical & Regulatory Knowledge
In-depth knowledge of sterile product manufacturing regulations for global markets.
Proven ability to lead and prepare teams for regulatory body audits.
Strong understanding of cGMP requirements.
Skills & Competencies
Excellent leadership and team development skills.
Strong problem-solving and analytical abilities.
Effective communication and presentation skills.
Project management expertise.
Proficiency in Microsoft Office Suite.
Ability to identify and focus on key elements of complex problems.
Willingness to travel or temporarily relocate as required.
Our Benefits Include
Highly competitive salary
Group pension scheme - Contribution rates are (1.5% / 3%/ 5%/ 7%) and company will match
Private Medical Insurance for the employee
Ongoing opportunities for career development in a rapidly expanding work environment
Succession planning and internal promotions
Education allowance
Wellness activities - Social activities such as Padel, Summer Events
Location: Grange Castle International Business Park, Grange, Co.
Dublin, D22 K2R3
Learn more about Grifols
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