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 a IT Validation Technician like you.
Mission
The IT Validation Technician supports the execution of the defined validation methodologies which comply with company standards and regulatory requirements. This role also oversees teams and validation resources engaged in validation activities.
What your responsibilities will be
- Create, review, and update required documentation for changes and projects as assigned in accordance with IT Methodology.
- Help to ensure that validation plans are agreed prior to execution and all plan requirements are fulfilled and approved upon completion of each validation step.
- Ensure IT quality, legal, and regulatory compliance through adherence to quality control standards in all activities.
- Monitor and address assigned issues to ensure timely resolution; updates stakeholders regularly on progress.
- Support the execution of a clear, concise, documented process for the assessment and validation of system implementations, changes, and/or integration of technologies.
- Assist in maintaining and evolving the validation documentation of the systems, assuring that the documentation is up to date and compliant with current regulations.
- Support the application of standards for validation protocols which meet global/local legal and regulatory requirements.
- Ensure compliance with technology policies and regulatory requirements and take appropriate action to mitigate risks and resolve issues.
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 accommodation may be made to enable individuals with disabilities to perform the essential functions).
- Bachelor’s degree in Life Sciences (Biology, Pharmacy, Biotechnology, Chemical or a related discipline).
- Hands-on experience of 1-3 years of proven experience working within a regulated pharmaceutical environment, including GxP compliance.
- Solid understanding of project management methodologies, tools, and best practices.
- Knowledge of regulatory requirements and GxP standards applicable to computerized systems.
- Experience supporting regulatory inspections and audit responses.
- Strong attention to detail with the ability to manage multiple priorities simultaneously.
- Ability to work both independently and collaboratively in cross-functional and international teams.
- Excellent organizational, communication, and problem-solving skills.
- Advanced in English, with the ability to work effectively in an international environment.
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 www.grifols.com. If you are interested in joining our company and you have what it takes for such an exciting position, then don’t hesitate to apply!
We look forward to receiving your application!
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.
Flexibility for U Program: Hybrid Model
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h (with the same flexible start time).
Benefits package
Contract of Employment: Permanent position
Location: SPAIN : España : Parets del Valles:[[cust_building]]
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