https://www.disjob.com/ utiliza cookies analíticas y de sesión con la finalidad de prestar un mejor servicio. No obstante, necesitamos su consentimiento explícito para poder utilizarlas. Así mismo puede cambiar la configuración de las cookies u obtener más información aquí.
*IMPORTANTE: Sí, estoy en posesión del CERTIFICADO DE GRADO DE DISCAPACIDAD IGUAL o SUPERIOR AL 33% EN VIGOR.
Todas nuestras ofertas laborales son exclusivas para el Colectivo disCapacidad.
Recuerda que tu experiencia académica y profesional, debe coincidir con los requisitos solicitados por la empresa. En caso contrario, no serás considerado para el presente proceso, y puede condicionar tu candidatura de cara a futuros procesos de selección que abra esta compañía. Revisa tu currículo antes de inscribirte
Parets del Vallès
TIPO DE CONTRATO
DESCRIPCIÓN DE LA OFERTA
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.
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.
Information about Grifols is available at www.grifols.com. If you’re interested in joining our company and you have what it takes, then don’t hesitate to apply.
We look forward to receiving your application.
Grifols is an equal opportunity employer.
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
Contract of Employment: Permanent position
Flexibility for U Program: 2 days remote working
Servicios de diseño, ensayo, certificación e ingeniería para la industria del automóvil a escala mundial. Nuestra reputación se basa en la experiencia de un equipo internacional de más de 2.450 profesionales y expertos técnicos, en nuestras instalaciones, en nuestra orientación al cliente.