Operadores De Montaje - Control De Calidad (Inmediato)

Ras Tempo; Barcelona; In loco; EUR 52.000 - 71.000; Tempo pieno

Descrizione del lavoro

Grifols, a global healthcare leader, seeks a dedicated QA professional to strengthen our GCP/GCLP quality assurance programs in Barcelona. You will plan and conduct audits of CROs and vendors, review internal GCP processes, and prepare comprehensive audit reports to drive compliant practices across the organisation.

The role requires a Ph.D. or Master in life sciences, at least 2–3 years in GCP/GCLP QA, and willingness to travel. Fluent English is essential as part of our global team.

Competenze

• Requires Ph.D. or Master in life sciences or pharma.
• At least 2–3 years of practical experience in GCP/GCLP QA.
• Advanced English proficiency.

Mansioni

• Plan and conduct audits of CROs and vendors.
• Perform internal reviews of clinical GCP processes.
• Prepare audit reports and track corrective actions.
• Provide guidance to Clinical staff on audit findings.
• Support inspections by regulatory agencies.

Conoscenze

GCP QA

GCLP QA

Quality Assurance

Compliance

Formazione

Ph.D./Masters in pharmaceuticals or life sciences

Descrizione del lavoro

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.

What your responsibilities will be

• Plan and conduct audits of CROs, vendors, investigator site audits. Assess compliance with applicable regulations and standards.
• Conduct internal audits of Clinical GCP processes for adherence to SOPs, company policy, and regulations/standards.
• Contribute to the review of the internal procedures related to the planning, conduct and oversight of clinical audits.
• Prepare audit reports and discuss findings with auditees and internal customers. Track and follow up on the resolution of audit findings.
• Provide guidance to Clinical staff in resolving audit findings in a compliant manner.
• Assist internal groups in preparing for inspections by regulatory agencies and participate in on site regulatory inspections as appropriate.

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 Ph.D. Master, Bachelors in pharmaceuticals or life sciences related field.
• You have at least 2-3 years of practical experience in GCP and GCLP quality assurance or compliance.
• Your English is advanced.
• You have availability to travel.

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.

We believe in diverse talent and want to remove any barriers that may hinder your participation. If you require