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Grifols Shared Services North America, Inc MES Specialist in Dublin, Ireland

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:

The Manufacturing Specialist (MES) will be responsible for development, configuration and testing of Master Batch Records (MBRs) from initial to final design. The successful candidate will have at least three years’ experience with PAS-X Software.

KEY RESPONSIBILITIES

  • Responsible for the development, configuration and testing of Master Batch Records (MBRs) from initial to final design in PAS|X.

  • Responsible for leading MBR development design process improvement projects.

  • Responsible for training of Electronic Batch Record (EBR) end-users (Supervisors, Operators, Technical/QA/Support staff).

  • Responsible for the development, review, and update of MES Standard Operating Procedures.

  • Responsible for the preparation and management of MBR change requests and associated change request forms (and other documentation) in a timely manner by liaising with customers, System Owner, Quality, etc.

  • Accountable for adherence to established timelines and metrics for the deviation, change control and CAPA process.

  • Responsible for any applicable equipment integration design, configuration and testing to allow MBR interaction with shop floor equipment – SAP, OSI PI, PCS7.

  • Responsible for resolving interface errors and stock discrepancies between ERP/MES as required.

  • Responsible for providing technical support where required and as directed by Operations leadership

PERSON SPECIFICATION

  • Proven Experience in PAS|X Software Design & Configuration

  • 1 plus years’ experience in an operation’s pharmaceutical environment.

  • Working knowledge of operations in pharmaceutical/biotech industries or aseptic processing an advantage

  • Knowledge of regulation requirements (GMP & IT/System Integration, etc)

  • Experience with PAS|X ERP Interface (SAP)

  • Experience with OSi Pi software is an advantage

QUALIFICATIONS

  • Bachelor’s degree in Engineering or Science or related industry qualification

  • PAS|X PRO Training Certification - desire

What we offer

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

Our Benefits Include:

  • Highly competitive salary

  • Group pension scheme - Contribution rates are 5% employer and 5% employee

  • 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 eg. Padel, Summer Event

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

#LI-FD1

Grange Castle Business Park in Clondalkin.

Learn more about Grifols (http://www.grifols.com/es/web/international/home)

Req ID: 516340

Type: Regular Full-Time

Job Category:

DirectEmployers