Pharma Quality Auditor

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions).

• You have a Life Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology) or Engineering Degree (Chemical or Industrial) or 10 years experience.
• You have 3-5 years of experience in GDP within pharmaceutical industry.
• High valuable to have experience in Auditing GxP.
• Strong analytical and communication skills.
• Availability to travel approximately 30%.
• Advanced English level, both written and spoken.

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.

Information about Grifols is available at www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don't hesitate to apply!

We look forward to receiving your application!

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help.

Grifols is an equal opportunity employer.

Contract of Employment: Permanent position

Location: Sant Cugat del Vallès.

www.grifols.com

Location: SPAIN : España : Sant Cugat del Valles:[[cust_building]]

Learn more about Grifols

From Quality Assurance we are looking for a Corporate Quality Auditor who will be the responsible to perform the Corporate Quality audits to the companies of Grifols Industrial group and affiliates, in order to evaluate and ensure the compliance of Good Distribution Practices, internal procedures and internal policies as well as to detect opportunities for improvement and best practices. Audits will be performed to Biopharma, Diagnostic and Healthcare busines units manufacturing sites (Pharmaceutical products and Medical Devices) and Grifols Affiliates.

• Collect and review all documentation required to prepare and execute audit activities.
• Define and coordinate the audit agenda, ensuring alignment with audit objectives and stakeholders.
• Prepare all audit-related documentation prior to audit execution, including checklists, working papers, and supporting materials.
• Conduct Corporate Quality Audits, ensuring compliance with the approved audit plan, scope, and timelines.
• Prepare comprehensive audit reports, clearly documenting activities performed, identified risks, findings, and opportunities for improvement in a timely manner.
• Evaluate, classify, and document audit findings according to established quality standards, providing practical recommendations for improvement.
• Follow up on corrective and preventive actions (CAPAs) derived from audits, monitoring implementation and effectiveness.
• Support the management, monitoring, and reporting of quality indicators and key performance metrics within the area.
• Collaborate with internal stakeholders to promote continuous improvement and compliance across the organization.
• Ensure adherence to corporate quality standards, regulatory requirements, and internal procedures throughout the audit process.

Flexibility for U Program: Hybrid Model

Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h. (with the same flexible start time).