Quality Assurance Senior Associate, Biopharma (JP10382)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 2, 2026
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Job Description:
Job Title: Quality Assurance Senior Associate, Biopharma
(JP10382) Location: Thousand Oaks, CA. 91320 Employment Type:
Contract Business Unit: Drug Product Quality Assurance Duration: 12
months with likely extensions Rate : $28-32/Hr W2. Posting Date:
06/07/22 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: This
position supports Quality Assurance program under the Plant QA
organization providing daily oversight of the Drug Product
manufacturing areas. Under general supervision, the role provides
support and compliance oversight to Manufacturing and Facilities &
Engineering staff in the execution of their processes, procedures,
and use of quality systems. Duties include purposeful presence on
the shop floor, electronic batch record creation, batch record
review, SOP revision approval, work order approval, and quality
approval of minor deviations and CAPA records. Responsibilities
will include evaluation of compliance issues, providing
recommendations, and assuring progress of quality records to
completion. The Sr. Associate will also represent functional area
quality for the Drug Product Quality Assurance department in the
execution of projects necessary to achieve departmental operational
goals and will work in a team matrix environment. Preferred
Qualifications: Bachelor's Degree in Biochemistry, Biology,
Chemistry, or related science field. Demonstrated ability to
perform GMP operations including following detailed SOPS,
maintaining training, and good documentation practices. Experience
managing projects through to completion meeting timelines.
Evaluating documentation and operations according to company
procedures. Experience working with Quality Systems Strong
organizational skills and ability to manage multiple tasks at one
time Effective communication skills (both written and verbal)
Demonstrated ability to work as both a team player and
independently Display leadership attributes and drive improvement
initiatives. Solid understanding and application of aseptic
behaviors and principles Basic Qualifications: Master's degree and
1 years of Quality experience OR Bachelor's degree and 2 years of
Quality experience OR Associate's degree and 6 years of Quality
experience Why is the Position Open? Supplement additional workload
on team. Top Must-Have Skill Sets: Must have Pharma industry
experience Experience in manufacturing or quality fields within
biotech or pharma industries. Complex decision making skills,
ability to complete tasks autonomously, provide updates to area
manager, and identify potential issues. Technical writing skills
The ideal candidate would have applicable drug substance/drug
product bio-tech manufacturing facilities as a QA or from a
manufacturing background Day to Day Responsibilities: The role
provides support and compliance oversight to Manufacturing and
Facilities & Engineering staff in the execution of their processes,
procedures, and use of quality systems. Duties include purposeful
presence on the shop floor, electronic batch record creation, batch
record review, SOP revision approval, work order approval, and
quality approval of minor deviations and CAPA records.
Responsibilities will include evaluation of compliance issues,
providing recommendations, and assuring progress of quality records
to completion. The Sr. Associate will also represent functional
area quality for the Drug Product Quality Assurance department in
the execution of projects necessary to achieve departmental
operational goals and will work in a team matrix environment.
Employee Value Proposition: The person in this role will oversee a
drug product facility and interacts with different departments
outside of manufacturing Red Flags: Minimal to no experience
Interview process: Phone screening followed by panel interview. We
invite qualified candidates to send your resume to
recruiting@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, Altadena , Quality Assurance Senior Associate, Biopharma (JP10382), Science, Research & Development , Thousand Oaks, California
