Top 3 Must Have Skill Sets:
Day to Day Responsibilities:
- Experience working with Quality Systems / QA
- Ability to perform GMP operations
- Bachelor’s Degree in Biochemistry, Biology, Chemistry, or related science ﬁeld (strongly preferred)
This role supports Quality Assurance program providing daily oversight of Drug Substance manufacturing facilities at Thousand Oaks. Under general supervision, the role provides support and compliance oversight to MFG and F&E staff in the execution of their processes, procedures, and use of quality systems.
Duties include electronic batch record review, batch record review, SOP and MP revision approval, work order approval, and qual‐ ity approval of non-conformances and CAPAs. Responsibilities will include evaluation of compliance issues, providing recom‐ mendations, and assuring progress of quality records to completion. The incumbent will also represent functional area quality for the Bulk Quality Assurance department in the execution of projects necessary to achieve departmental operational excellence goals and will work in a team matrix environment.
Frequent job movement/ job hopping
phone screening followed by in-person or virtual interviews
PAY RATE : $33-$37/hr on W2
"This posting is for Contingent Worker, not an FTE"