Quality Assurance Senior Associate – (JP10240)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 6, 2026
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Job Description:
Job Title: Quality Assurance Senior Associate – (JP10240)
Location: Thousand Oaks, CA. 91320 Employment Type: Contract
Business Unit: Plant QA Drug Substances Duration: 18 months (with
likely extensions) Notes: 100% Onsite. Must have Biotech/ Pharma
experience required. Must be able to work swing, morning, evenings,
night shift (24/7 Operation building). Once trained it will 4 day
work week. Must have proven Quality Assurance experience. Must have
lab setting and quality background as they will be supporting the
lab staff and provide quality oversight. Posting Date: 05/10/22 3
Key Consulting is hiring a Quality Assurance Senior Associate for a
consulting engagement with our direct client, a leading global
biopharmaceutical company. Job Description: The Senior Associate QA
role supports client’s Quality Assurance program, providing daily
oversight of Drug Substance manufacturing facilities at client’s
Thousand Oaks, CA. facility. 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 purposeful presence on the manufacturing
floor, batch record review, SOP and MP revision approval, work
order approval, and quality approval of deviations and CAPAs.
Responsibilities will include evaluation of compliance issues,
providing recommendations, 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 to
ensure workplace safety. This staff member will be assigned to
provide quality support during either day or night shift schedule
periods, as operation support is 24/7. Why is the Position Open?
Supplement additional workload on team. Top Must-Have Skill Sets:
Technical writing experience (i.e. deviation records, CAPA records,
controlled documents) Excellent verbal and written cross functional
communication skills Must have biotech/pharma manufacturing,
quality assurance, or quality control experience Biotech/ Pharma
experience required Must be able to work swing, morning, evenings,
night shift (24/7 Operation building). Once trained it will 4 day
work week. Day to Day Responsibilities: Purposeful presence on the
manufacturing floor (80% of working time spent on MFG floor in
controlled, classified cell culture and protein purification
areas). Batch record review SOP and MP revision approval work order
approval quality approval of deviations and CAPAs Safety auditing
and observational work GEMBA walks Red Flags: Not able to work
onsite Unable to work shifts including morning, evening, or
potentially nights No Biotech/ Pharma background/experience No
quality assurance, quality control experience Interview process:
Phone screening followed by in-person interview. We invite
qualified candidates to send your resume to
resumes@3keyconsulting.com . If you decide that you’re not
interested in pursuing this particular position, please feel free
to take a look at the other positions on our website
www.3keyconsulting.com/careers. You are also welcome to share this
opportunity with anyone you think might be interested in applying
for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Altadena , Quality Assurance Senior Associate – (JP10240), Science, Research & Development , Thousand Oaks, California
