Pharmacovigilance QA Specialist

TN Spain; Sant Cugat del Vallès; Presencial; EUR 35.000 - 65.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Pharmacovigilance QA Specialist to join their Clinical Quality Assurance team. This role offers a unique opportunity to work within a global healthcare company dedicated to improving lives through innovative medicines. You will conduct audits, analyze compliance issues, and support training initiatives, all while collaborating with a dedicated team. If you are proactive, analytical, and possess strong communication skills, this position could be the perfect fit for you. Join a company that values diversity and fosters an inclusive work environment, and take the next step in your professional career.

Formación

• 3-5 years of experience in pharmacovigilance and audits in a pharmaceutical company.
• Proficiency in English (C1.1) and strong communication skills.

Responsabilidades

• Conduct audits to support compliance with good pharmacovigilance practices.
• Analyze deviations and manage CAPAs effectively.

Conocimientos

Pharmacovigilance

Auditing

Analytical Skills

Communication Skills

Teamwork

Educación

Bachelor's degree in Health Sciences

Descripción del empleo

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Client:

Grifols

Location:

Job Category:

Other

EU work permit required:

Yes

Job Views:

Posted:

Expiry Date:

17.05.2025

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 that foster an inclusive environment.

For Grifols’s Scientific Innovation Office, we are seeking a Pharmacovigilance QA Specialist to collaborate with our Clinical Quality Assurance team:

What your responsibilities will be

• You will conduct audits according to the plan established to support compliance with good pharmacovigilance practices (GVP).
• You will work with Global Pharmacovigilance (GPV) Staff to resolve audit findings and offer suggestions for improvement.
• You will analyze deviations and CAPAs Management.
• You will support the Pharmacovigilance staff regarding compliance issues within the area of expertise.
• You will support the development of training plans and review of SOPs and documentation generated by GPV.

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 accommodations may be made to enable individuals with disabilities to perform the essential functions.

• You have a Bachelor's degree in Health Sciences. Specialization in pharmacovigilance and/or audits is a plus.
• You have 3 to 5 years of experience in pharmacovigilance and/or audits within a pharmaceutical company.
• You have advanced English proficiency (C1.1).
• You are proactive, a team player, and have strong written and oral communication skills.
• You are rigorous and analytical.

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.

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!