Quality Auditor
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Job Summary
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. |
Help us lead one of the worlds 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. Thats why we need aQuality Auditorlike you.
Misión del Rol
Perform the planning preparation execution follow-up and closure of GMP audits both internal and for plasma suppliers and related services as well as the coordination of external audits (clients certifying bodies etc.) and regulatory inspections ensuring proper documentation regulatory compliance and the continuous improvement of the quality system and the management of quality indicators within the area.
What your responsibilities will be
- Plan prepare execute and follow -up internal a external cGMP audits.
- Generate study protocols reports and standard departmental documentation.
- Provide guidance and coordination to the team on specific work activities.
- Ensure knowledge and application of applicable working standards (GMP SOPs internal guidelines GLP etc.) in line with established procedures.
- Ensure accurate completion of records when required.
- Adhere to quality safety hygiene and environmental regulations and standards.
- Report any incidents impacting normal operations to the direct supervisor.
- Perform tasks corresponding to lower professional levels when necessary.
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).
- Degree in Health Sciences (Pharmacy Biology Chemistry Biochemistry Biotechnology); Masters and/or PhD desirable.
- Minimum of 2 years experience in the pharmaceutical industry.
- You have knowledge of GMP GLP ICH and related guidelines.
- You are available to travel frequently (30%) both domestically and internationally depending on the audit projects.
- You have an advanced level of English (C1) indispensable.
- Strong time management and prioritization skills.
- Excellent communication analytical skills and attention to detail.
- Strong ability to work effectively within a team.
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. If you are interested in joining our company and you have what it takes for such an exciting position then dont hesitate to apply!
We look forward to receiving your application!
Grifols is an equal opportunity employer.
Flexible schedule: Monday-Thursday 8:00h 17:00h and Friday 8:00 - 15:00h (with the same flexible start time).
Benefits package
Professional Group 06
Contract of Employment:Permanent position
Flexibility for U Program: Hybrid Model
Location: Parets del Vallès
Required Experience:
IC
About Company
Explore Grifols' comprehensive, innovative and patient-centric biopharma and healthcare solutions.
