Quality Auditor/a Pharma

hace 2 semanas

Barcelona, España Instituto Grifols SA A tiempo completo

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.**

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 an Auditor like you.

Instituto Grifols S.A. is looking for a **_Quality Auditor_**, which role mission** **will be a person in charge of managing internal, supplier and external or inspections audits based on GMP regulations. Furthermore will be part of different projects or taking part of global groups of the company among others.

**What your responsibilities will be**
- Collaborate in the process of planning, preparation and execution of internal audits as well as the correct documentation of the same.
- Participate in the process of planning, preparation and execution of audits to suppliers of products, services and outsourced activities as well as the correct documentation of the same.
- Collaborate in the process of planning, preparation and execution of the audits to be performed in the R&D area as well as the review as a quality assurance unit of the protocols and technical reports generated by this area that require it and are aligned with the NCF.
- Follow-up of corrective and/or preventive actions derived from internal and external audits, official inspections by regulatory agencies and all those generated in the R&D area.
- Participate in the process of preparation and coordination of inspections by certifying bodies and health/regulatory authorities or audits by external companies.

**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).
- BA/BS in Lifesciences Required.
- Minimum 3 years of experience.
- Pharma/biotech experience strongly preferred.
- Native Spanish and Advance English.
- Strong written and verbal communication skills.
- Ability to work under pressure, problem solving, analytical skills, negotiation skills, assertiveness, communication skills, pro-activity, establishing trusting and interdepartmental relationships, organizational skills.
- Own car.
- Availability to travel, not to exceed 20% of the annual working day.

**What we offer**

It’s a brilliant opportunity for someone with the right talents.

Grifols understands you want a challenging and rewarding career in a critical function such as Corporate Communications. We’ll help you grow professionally.

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**:Parets del Vallès

**Location**:SPAIN : España : Parets del Valles**:P3**

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