Quality Assurance Senior Associate – (JP10393)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 1, 2026
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Job Description:
Job Title: Quality Assurance Senior Associate – (JP10393)
Location: Thousand Oaks, CA. 91320 Employment Type: Contract
Business Unit: Plant QA Drug Substances Duration: 18 months (with
likely extensions) Rate : $28-32/Hr W2. 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: 06/02/22 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, Irvine , Quality Assurance Senior Associate – (JP10393), Science, Research & Development , Thousand Oaks, California
