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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 opportunities, fostering an inclusive environment where diversity makes us 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 R&D QA Specialist & Auditor like you. Provide quality oversight of SIO pre-clinical activities to ensure that studies, processes, systems and documentation comply with applicable regulatory requirements, company standards and the R&D Quality System. Review of study documentation and data, quality oversight of SIO pre-clinical activities, execution of internal and external audits, qualification and oversight of vendors and management of quality system processes such as deviations, CAPAs, change controls and controlled documentation. Support development programs through independent quality oversight and audit activities, identify compliance risks, drive continuous improvement initiatives and provide QA guidance to cross-functional teams to ensure the integrity, reliability, and regulatory acceptability of SIO pre-clinical activities for plasma and non-plasma products. 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 accommodation may be made to enable individuals with disabilities to perform the essential functions). Bachelor’s degree in a Health Sciences-related field, such as Biology, Biochemistry, Chemistry, Biomedical Engineering, or a similar discipline. You have 2-5 years of experience in the pharmaceutical industry in a similar Quality Assurance (QA) role or within scientific research environments applying GLP regulations. Strong knowledge of GCLP, GMP and GLP quality standards and regulatory requirements. Advanced English proficiency. Advanced user of Microsoft Office tools, including Word, Excel and Outlook, with solid knowledge of Quality Management Systems (QMS), particularly within SAP environments and Document Management Systems (DMS). 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. 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. Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time). Contract of Employment: Permanent position Flexibility for U Program: Hybrid Location: Sant Cugat del Vallès Type: Indefinido tiempo completo www.grifols.com Learn more about Grifols #J-18808-Ljbffr

That’s why we need R&D QA Specialist & Auditor like you.

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. It is a brilliant

BOLD is committed to shaping the future of high-performance mobility from Formula 1 to aviation and marine. In our mission to deliver innovative and impactful products in the mobility sector, we are building the company whilst working with clients in exciting engineering and manufacturing challenges. As a Supplier Quality Engineer, you will liaise with all our current and future suppliers. You will validate any new parts or suppliers against production and customer requirements as well as our quality standards. You will manage supplier nonconformities based on root cause analysis in order to avoid recurrence. • Evaluate and validate new suppliers to be part of BOLD's supplier panel., • Analyze and evaluate special customer-relevant quality requirements., • Provide input and liaise with suppliers during the RFI and RFQ stages of the acquisition phase., • Analyze and implement requirements for purchased parts in new developments and technical changes., • Manage supplier PPAP and purchased part related APQP., • Supplier Quality Management from acquisition phase to SOP and during production., • Perform Supplier audits and assist engineering and procurement teams from the quality point of view., • Product and process validation for new components at supplier site -, • Initiate and follow through to completion any supplier NCR., • Travel up to 60% to suppliers (mainly in Spain)., • 5+ years of experience as Supplier Quality Engineer., • Bachelor's degree (or higher) in Electric, Electronic or Industrial Engineering, or equivalent professional work experience., • Experience with Automotive and/or Aerospace standards at production level with IATF16949, AS9100 certification., • Deep knowledge and experience in the use of core tools (problem solving, APQP, PPAP, FMEA, 8D, etc.)., • Driver's license and own vehicle., • Expertise in electric and/or electronic components., • Experience with battery packs., • Understanding the testing requirements and validating battery products at a high level., • Auditor VDA 6.3., • Competitive compensation., • Flexible compensation, • Health insurance., • Kindergarten., • Regular events and team building activities. BOLD is an equal opportunity company. We believe in a merit and competence culture where the best ideas thrive regardless of age, disability, race, religion, or belief, gender, sexual orientation, marital status, or family circumstances. #J-18808-Ljbffr

Grifols is seeking an R&D QA Specialist & Auditor to oversee pre-clinical activities for plasma and non-plasma products.

R&D QA Specialist & Auditor to provide quality oversight of SIO pre-clinical activities, ensuring studies, processes and documentation comply with regulatory requirements and Grifols standards.

Grifols is seeking a QA Specialist & Auditor to join its international team in Sant Cugat del Vallès.

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R&D QA Specialist & Auditor to provide quality oversight of SIO pre-clinical activities, ensuring studies, processes and documentation comply with regulatory requirements and Grifols standards.

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