Description
Quality, Service, Collaboration, Courage
Do you exhibit these values and wish to be around others that do? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture?
Job SUMMARY:
Support quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include but are not limited to: provide on the floor oversight and general support for the manufacturing of aseptic processes, deviation and CAPA systems, batch record review, SOP creation and revision, review of quality documents, and supporting the Quality Management System.
Full job description available during formal interview process.
REQUIREMENTS:
Knowledge of QA Principles in a pharma, biopharma, or biotech manufacturing environment
Bachelor's Degree in life sciences or related field
Minimum of 2 years related work experience
What we offer you:
BENEFITS Starting day 1! Blue Cross/Blue Shield medical and dental with the company paying for 75% of the cost is available to you and your family on your first day of work. We also offer vision, life, disability, a 401(k) program, and off-shift premiums.
Paid VOLUNTEERISM Starting day 1! GRAM encourages giving back to your community by offering 16 hours of volunteer time per calendar year.
PTO! Full-time employees accrue up to 3 weeks of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
HOLIDAYS: We celebrate diversity in offering 8 paid holiday per calendar year.
Pay: DOE
GRAM supports Equal Opportunity Employment
