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Join to apply for the Pharmacovigilance QA Specialist role at Grifols
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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 opportunity fostering an inclusive environment where diversity makes us be outstanding.
Help us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Pharmacovigilance QA Specialist like you.
What Your Responsibilities Will Be
* You will conduct audits according to 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 manage deviations and CAPAs.
* You will support and advise the Pharmacovigilance staff regarding compliance issues within the area of expertise.
* You will support the 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.
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.
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
Benefits Package
Contract of Employment: Permanent position
Flexibility for U Program: 2 days remote working
Location: Sant Cugat del Vallès
www.grifols.com
Location: SPAIN : España : Sant Cugat del Valles : [[cust_building]]
Learn more about Grifols
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Contract
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing and Medical Equipment Manufacturing
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