FAQs
What is the role of the Validation Intern at Grifols?
The Validation Intern will assist in the validation and qualification of existing and new systems used in the pharmaceutical manufacturing area, including organizing documents, maintaining validation files, and supporting the completion of validation reports.
What educational background is required for this internship?
Candidates must be currently enrolled in a 4-year degree program pursuing a Bachelor's degree in Business/Marketing or a scientific field (Biology/Chemistry preferred), or they must be currently accepted or enrolled in a Master's or PhD program.
Is there a GPA requirement for applicants?
Yes, candidates must currently have a GPA of 3.0 or higher.
What skills are preferred for this internship?
Familiarity and comfort with Excel (including working with Macros and pivot tables), as well as proficiency in Microsoft Word and PowerPoint, are preferred skills for this position.
Where is this internship located?
The internship is located in Los Angeles, California, at the Grifols Valley Bl Manufacturing Plant.
Are there any specific tasks mentioned for the Validation Intern?
Yes, specific tasks include organizing and archiving validation reports, checking inventory of test materials, assisting in housekeeping of validation workspaces, and making copies of supporting documents.
Is there an opportunity for career growth with Grifols?
Yes, Grifols is a global healthcare company with a long history in the industry, providing various opportunities for professional development and growth.
Does Grifols provide equal employment opportunities?
Yes, Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law.