FAQs
Is this position remote or on-site?
This is a fully on-site position in Vernon Hills, Illinois.
What qualifications are necessary for this role?
A BS degree in Chemistry or Biology is required, along with experience in GMP and the pharmaceutical industry.
What are the key skills needed for a QC Data Reviewer?
The must-have skills include HPLC and UPLC (chromatography) and data review experience.
What kind of work environment can I expect?
The company provides a full range of rapid testing and support services, focusing on pharmaceutical products and various compounded preparations across six major industries.
How does Actalent approach diversity and inclusion?
Actalent's DE&I initiatives include hiring diverse talent, maintaining an inclusive environment, building a culture of care and engagement, and ensuring growth opportunities for all employees.
Will I be required to communicate with other departments?
Yes, you will work closely with other departments and Quality Assurance staff to develop and document project requirements.
What software or systems will I work with in this role?
You will review ongoing testing, spreadsheets, electronic notebooks, Empower, and other software ensuring compliance with cGMP standards.
How can I request accommodations during the application process?
You can request reasonable accommodations by emailing actalentaccommodation@actalentservices.com for assistance with the application or interviewing process due to a disability.
Is previous experience in a quality assurance environment important?
Yes, participating in continuous improvements in a quality assurance environment is essential to detect issues and ensure requirements are met before information is released to clients.
What will my primary responsibilities include?
Your primary responsibilities will include routine communication on data review, ensuring documentation compliance, and assisting in quality assurance processes related to ongoing testing.