Pharma Production Operator - Rotating Shifts (Temp)

Esteve; Barcelona; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Hybrid model

Job summary

Grifols is seeking a Corporate Quality Auditor to perform corporate quality audits across the Grifols Industrial group and affiliates, ensuring GDP compliance, internal procedures, and continuous improvement.

The role requires a Life Sciences or Engineering degree, 3–5 years GDP experience, GxP auditing background, strong analytics, travel ~30%, and advanced English.

Qualifications

• Life Sciences or Engineering degree required.
• 3–5 years GDP experience in pharmaceutical industry.
• Experience auditing GxP desired.
• Strong analytical and communication skills.
• Willingness to travel ~30%.
• Advanced English level (written and spoken).

Responsibilities

• Conduct Corporate Quality Audits across Grifols Industrial group and affiliates.
• Prepare and coordinate audit agendas and documentation.
• Prepare audit reports with findings and improvement recommendations.
• Follow up on CAPAs and monitor effectiveness.
• Support management and reporting of quality indicators and KPIs.
• Promote continuous improvement and regulatory compliance across the organization.

Skills

Analytical skills

Advanced English

Travel readiness

Education

Life Sciences degree

Engineering degree (Chemical/Industrial)

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.

We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding.

Mission

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.

What your responsibilities will be

• 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.

Who you are

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.

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.

Information about Grifols is available at

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.

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).

Benefits package

Contract of Employment: Permanent position

Location: Sant Cugat del Vallès.

more about Grifols ( ID:

Type: Indefinido tiempo completo

Job Category: Calidad