Quality Auditor
hace 3 días
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.**
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 Manufacturing Practices, Good Distribution Practices, internal procedures and internal policies as well as to detect opportunities for improvement and best practices. Audits will be performed to Bioscience, Diagnostic and Hospital division manufacturing sites (Pharmaceutical products and Medical Devices) and Grifols Affiliates.
**What your responsibilities will be**
- Collect the documents required to prepare the audits.
- Define the Audit agenda.
- Prepare the documents associated to audit, before it is performed (check list, working sheets, etc).
- To Conduct the Corporate Quality Audits performance, ensuring the audit plan established in the agenda is accomplished.
- Write the Audit Report with the relevant activities carried out in the audited company identifying the associated risks and opportunities of improvements, in a timely manner.
- Classify the findings and writing recommendations.
- Look at the corrective and preventive actions derived from the audit.
- To support the indicators management of the area.
**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 Life Sciences Degree (Pharmacy, Biology, Chemistry, Biotechnology, ) or Engineering Degree.
- You have 3-5 years of experience in GMP, auditing factories within pharmaceutical / medical devices / sterile products industry.
- You have a high proven knowledge of GMP.
- Your English is advance.
- You are available to travel (approximately 30%).
**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.
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.
**Benefits package**
**Contract of Employment**: Permanent position
**Location**:Sant Cugat del Vallès
Third Party Agency and Recruiter Notice:
**Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other characteristic or status protected by law.** We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance.**
**Location**:SPAIN : España : Sant Cugat del Valles**:SC3**
Learn more about Grifols
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