Table.MiTabla { max-width: 1020px;!important
Obtenga más información sobre este puesto leyendo los detalles a continuación y luego envíe su solicitud para ser considerado.
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 a
Bioanalytics Scientist,
like you.
Misión del Rol
Her main responsibility will be to initiate, plan, coordinate, and execute the technical aspects of assigned projects within the established timelines. She will ensure that all developments, validations, and related activities are carried out in accordance with internal procedures and GMP regulations.
What Your Responsibilities Will Be
Plan, organize, and prioritize laboratory activities and assigned project tasks to ensure timely and high-quality delivery.
Manage, maintain, and ensure the proper functioning of laboratory equipment, instruments, and facilities.
Review and verify analytical results and/or experimental processes associated with assigned projects.
Provide technical guidance and support to other team members on specific laboratory methodologies and procedures.
Ensure that analytical procedures are appropriate, validated, robust, and suitable for transferability between laboratories.
Prepare, review, and approve technical documentation and general R&D documentation in compliance with internal and regulatory standards.
Review study protocols, validation reports, and technical procedures, taking ownership and accountability for their content and accuracy.
Oversee project-related requirements and ensure that all technical documentation included in regulatory submissions is complete and accurate.
Maintain and update general R&D documentation ensuring compliance with applicable quality systems and regulations.
Ensure that all personnel involved understand and correctly follow approved procedures and protocols.
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).
Degree in Health Sciences (Pharmacy, Biology, Chemistry, Biochemistry, Biotechnology); Master’s and/or PhD desirable.
3 years of experience in the pharmaceutical industry, preferably in bioanalysis, stability, analytical development, or quality control within a regulated environment.
Solid knowledge of GMP, GLP, ICH guidelines, and other applicable regulatory standards.
Experience in the execution, review, and documentation of analytical and/or stability studies.
Ability to interpret and critically review analytical results, ensuring data quality, traceability, and robustness.
Experience in preparing and reviewing technical documentation (study protocols, reports, validation documents, and regulatory submissions).
Proficiency in Microsoft Office tools (especially Excel) and quality management systems such as SAP QM or similar platforms.
Minimum English level B2.
Strong organizational and time management skills, with the ability to prioritize tasks in a multi-project environment.
Excellent communication skills, analytical thinking, and strong attention to detail.
Proven ability to work effectively within multidisciplinary and regulated team environments.
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 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!
Grifols is an equal opportunity employer. xpzdshu
Flexible schedule:
Monday-Thursday 8:00h – 17:00h and Friday 8:00 - 15:00h (with the same flexible start time).
Benefits Package
Contract of Employment:
Permanent position
Flexibility for U Program:
Hybrid Model
Location: Parets del Vallès
more about Grifols
#J-18808-Ljbffr