FAQs
What is the role of the Validation Intern?
The Validation Intern will assist in the validation and qualification of systems used in pharmaceutical manufacturing, including organizing raw data, archiving validation reports, and maintaining the validation workstation.
What are the main responsibilities of this position?
Main responsibilities include organizing, scanning and archiving validation reports, assisting with archival activities, checking inventory of test materials, and facilitating the completion of validation reports.
What are the educational requirements for this internship?
Candidates must be currently enrolled in a four-year degree program pursuing a Bachelor’s degree in Business/Marketing or a scientific field (Biology or Chemistry preferred) as a rising junior or senior, or must be currently accepted or enrolled in a Master’s or PhD program.
Is there a GPA requirement for applicants?
Yes, candidates must have a GPA of 3.0 or higher.
What technical skills are required for the Validation Intern position?
Familiarity/comfort with Excel, including working with Macros and pivot tables, as well as proficiency in Microsoft Word and PowerPoint, is required.
Where is the internship location?
The internship is located in Clayton, North Carolina, USA.
Are third-party agencies allowed to submit candidates for this internship?
Yes, but only if they have a valid Grifols Agency Master Services Agreement and have been engaged by a Grifols Recruiter to submit candidates for this position.
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.
Is this position suitable for students?
Yes, this internship is designed for students currently enrolled in relevant degree programs.