Quality Assurance Associate, Biopharma Medical Device (JP9524)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 1, 2026
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Job Description:
Job Title: Quality Assurance Associate, Biopharma Medical Device
(JP9524) Location: Thousand Oaks, CA. Onsite Employment Type:
Contract Business Unit: Plant Quality Assurance Incoming and
Packaging Duration: 2 years with possible extension or conversion
to FTE Posting Date: 12/14/2021 3 Key Consulting is hiring a
Quality Assurance Associate for a consulting engagement with our
direct client, a leading global biopharmaceutical company. Job
Description: This position will provide operational QA support of a
clinical drug product packaging and labeling team. Primary
responsibilities will include review and approval of printed
clinical labels, finished clinical pack inspection, expiration date
calculation and batch record review. Secondary responsibilities
will include generation and compilation of quality data and reports
(e.g. lot track/trace, deviations). Individual will also assist
with procedure reviews and initiation of deviation reports. There
is the potential for role expansion into support of a product
distribution function. Skills: quality assurance or manufacturing
experience in the pharmaceutical or medical device industry Must
have experience with GMP processes and documentation. Without that
fundamental skillset the training for document review tasks, label
approval and packaging inspection will have no foundation. Must be
able to methodically and meticulously inspect printed materials for
print quality defects, clinical product components (e.g. syringes
and vials) for physical defects, and batch record documentation for
accuracy and completeness. Must be able to work in a team with
shifting priorities and shifting responsibilities, such that the
team members must be confident verbal communicators able to discuss
responsibilities, divide them, reassess them, and potentially
reassign them throughout the day or week. Top Must-Have Skill Sets:
1 GMP processes and documentation experience Good Manufacturing
practices Inspection and QA background. Attention to detail; assign
expiration dates on labels, providing info on labels, and
documentation Packaging experience, is preferred Day to Day
Responsibilities: Primary responsibilities will include review and
approval of printed clinical labels, finished clinical pack
inspection, expiration date calculation and batch record review.
Secondary responsibilities will include generation and compilation
of quality data and reports (e.g. lot track/trace, deviations).
Individual will also assist with procedure reviews and initiation
of deviation reports. There is also the potential for role
expansion into support of a product distribution function. Employee
Value Proposition: Good team atmosphere and supportive team
Opportunity to learn and grow Red Flags: * Jumping from position to
position * Lack of attention of details * A minimum of 1 year of
experience in Quality Assurance Interview process: Phone screen
Virtual 1:1 (45 minutes- 60) with panel We invite qualified
candidates to send your resume to resumes@3keyconsulting.com . If
you decide that you’re not interested in pursuing this position,
please feel free to take a look at the other positions on our
website www.3keyconsulting.com/careers. You are welcome to also
share this opportunity with anyone you think might be interested in
applying for this role. Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Santa Clarita , Quality Assurance Associate, Biopharma Medical Device (JP9524), Science, Research & Development , Thousand Oaks, California
