FAQs
What is the primary responsibility of a Quality Assurance Technician at Actalent?
The primary responsibility is to provide direct manufacturing Quality Assurance support for all GMP activities, acting as a key Quality contact to manufacturing for discrepancy management, batch review, and line support.
What qualifications are required to apply for the Quality Assurance Technician position?
A B.A. or B.S. degree (preferably in Life Science) and 2-3 years of experience in the pharmaceutical, biopharmaceutical, or related industry, or an equivalent combination of education and experience are required.
What kind of laboratory experience is necessary for this role?
Hands-on industrial laboratory experience with analytical techniques such as HPLC and Mass Spectroscopy is necessary for this role.
Are there opportunities for professional development in this position?
Yes, there are opportunities for ongoing professional development, performance feedback, and career advice available to eligible employees.
What benefits does Actalent offer?
Actalent offers medical, dental, and vision insurance, six paid legal holidays, and paid time off.
Is there an emphasis on diversity and inclusion at Actalent?
Yes, diversity and inclusion are integral to Actalent's culture, with initiatives focused on hiring diverse talent, maintaining an inclusive environment, and ensuring growth opportunities for all employees.
What analytical techniques should a candidate be familiar with?
A candidate should be familiar with biochemical assays, high-performance liquid chromatography (HPLC), and mass spectroscopy.
How does Actalent handle accommodations for applicants with disabilities?
Actalent provides reasonable accommodations in the job application and interviewing process. Applicants can email actalentaccommodation@actalentservices.com for accommodation options.