Quality Audit Intern

Manpower Ireland is currently recruiting for a Quality Audit Intern with Grifols. Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. They 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.

Grifols Worldwide Operations Ltd. was established in 2012. Based in Dublin, they offer a comprehensive portfolio of Biopharma products and services worldwide.

It serves as the management center for Grifols Biopharma overseeing the treasury, risk management, supply and demand planning, regulatory, R&D, and commercial functions.

It also serves as a hub for labeling, packing, final conditioning, and distribution of finished plasma products to Grifols' worldwide network of commercial subsidiaries and distributors, with the exception of Spain and the United States.

Reporting to the Director, the Quality Audit Intern is responsible for quality activities within External Supplier Management & Internal Audit Quality Systems within the Global Quality Audits Department.

The purpose of this role is to assist in daily and monthly activities supporting both the external supplier programme and the internal audit schedule. This role will give the candidate a broad overview of Supplier Management operations and Internal Audit Quality Systems, as well as the critical interdepartmental responsibilities and communication to deliver business performance.

What's Involved:

Internal Audits

• Assist in the schedule adherence of the audit schedule.
• Train and participate within departmental audits.
• Attend monthly meetings in relation to audits.
• Assist in any follow ups regarding audits.
• Assist in the generation of audit metrics.

Supplier Management

• Continued maintenance of the Approved Supplier Audit Schedule.
• To provide support in generating supplier qualification reports.
• Communicate with cross functional departments on-site and across other Busines Units.
• Contribution to the continuous improvement of the Quality System.
• Compilation of site metrics to support Quality functions
• Write, execute, and approve relevant documentation of area specific documentation (including procedures, protocols, schedules etc.).
• Attend monthly meetings on Supplier Management.
• Other duties as required and directed by the Director Global Quality Audits.

Communication

• Liaise with overall Quality department and cross functional departments as required.
• Provide quality performance information as required.
• Participate fully in any cross functional training initiatives.

Who you are:

• Leaving Certificate or equivalent.
• Currently studying towards a 3rd level degree within the Pharmaceutical / Life Sciences or other relevant disciplines.
• Excellent communication and teamwork.
• Ability to work proactively on own initiative.
• Problem solving skills.
• Professional, proactive demeanour.
• Strong interpersonal skills.
• Excellent written and verbal communication skills.

Interested candidates are invited to submit their resume and a cover letter explaining their interest in the Quality Audit position at Grifols.