Manufacturing Filling Technician

Grifols; Dublin; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Competitive salary

Group pension

Private medical

Career development

Internal promotion

Education allowance

Wellness events

Job summary

Grifols in Ireland is seeking a Manufacturing Filling Technician to join an aseptic production team. The role covers operation, cleaning, and upkeep of equipment, ensuring cGMP adherence and accurate documentation in a fast-paced facility.

The ideal candidate has a scientific degree or equivalent experience, GMP exposure, and the ability to work shifts while supporting continuous improvement and quality investigations across the manufacturing process.

Qualifications

• Bachelor's degree in a scientific discipline is preferred.
• At least 2 years' related pharmaceutical GMP or EU-regulated experience.
• Experience with CIP/SIP, filtration systems, and SCADA-controlled systems.
• Solid knowledge of cGMP, GDP, and data integrity.
• Willingness to work shifts.

Responsibilities

• Operate and maintain aseptic processing equipment in GMP environment.
• Ensure gowning and cleanroom practices are followed; report non-conformances.
• Coordinate setup and troubleshooting of processing equipment.
• Clean and maintain facilities; ensure accurate documentation.
• Contribute to CAPA, deviations, and change controls.
• Train peers and keep training records up to date.
• Support production planning and supply chain requirements.
• Make timely area-specific decisions.

Skills

GMP experience

CIP/SIP

SCADA systems

Data integrity

Regulatory knowledge

GDP knowledge

Shift flexibility

Education

Bachelor's degree

Job description

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? 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.

Position Summary:

Reporting to Filling Supervisor, the Manufacturing Filling Technician is responsible for the operation, cleaning and upkeep of all equipment and facilities in an aseptic environment in support of manufacturing requirements. This person is also responsible for the adherence to, and leadership of, all cGMP, training and safety standards for the work area.

What You Will Do:

• Adhere to procedures and practices and maintain compliance with applicable departmental, corporate, industrial, health & safety and regulatory requirements.
• Ensuring that the gowning philosophies for all cleanroom, production and facility areas are strictly adhered to and all non-conformances are immediately actioned and reported.
• Ownership for the setup, coordination, regulation and troubleshooting of processing equipment in an aseptic biologics processing environment for plasma derived pharmaceuticals.
• Responsible for the cleaning (Manual and automated CIP/SIP) and upkeep of all associated facilities and equipment and for ensuring all areas are maintained in proper working order.
• Responsible for the accuracy and completeness of all Company documentation and material reconciliation.
• Maintain a safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures; complying with legal regulations; monitoring environment.
• Ability to operate automated scada-controlled/windows-based control systems in a GMP environment.
• Recommend and implement measures to improve production methods, equipment performance, facility layout, and quality of product. Actively participate in the company’s Continuous Improvement programs.
• Co-operate and support quality investigations and contribute to CAPA reporting and closure.
• Provide guidance and hands-on training to peers and colleagues and ensure all training records are up to date and in line with training SOP’s, OJT’s and policies.
• Capable of maintaining production without supervision, anticipates and adjusts for interventions, effectively manages multiple priorities.
• Meeting planning targets and supply chain requirements while improving on work practices, adjusting for multiple changing priorities.
• Making decisions specific to their area of work in a timely manner.

What You Will Bring:

• Bachelor's degree preferred in a scientific discipline.
• In lieu of a Bachelor’s degree, candidates must have a minimum of 2 years of related experience in a pharmaceutical, GMP, or EU regulated environment.
• 2+ years expereince working in a similar role in a pharmacuetical environment , in particular with CIP/SIPs, filtration systems and SCADA-controlled systems.
• Good understanding of cGMP, GDP, data integrity, regulatory requirements such as HPRA, FDA.
• Experience with deviation management, change controls, CAPAs
• Must be flexible to work shift as directed by the organization.

A proactive, results-driven self-starter with strong attention to detail, excellent organizational, analytical and problem-solving skills, able to effectively prioritize multiple tasks, exercise sound judgment, meet deadlines, and collaborate successfully with stakeholders across all levels.

Our Benefits Include:

• A highly competitive salary package
• Group pension scheme - Contribution rates are (3%/ 5%/ 7%) and company will match
• Private medical insurance for the employee
• Ongoing career development opportunities within a rapidly growing organisation
• Strong focus on succession planning and internal promotion
• Dedicated education and professional development allowance
• Wellness and social initiatives, including activities such as padel and summer events