Senior Associate Quality Assurance (Batch Record, CAPA, Deviations, GMP)

job
  • Aequor
Job Summary
Location
Thousand Oaks ,CA
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
03 Feb 2025
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Job Description

Job Title: MCS Senior Associate Quality Assurance

Location: Thousand Oaks, CA

Duration: 18+ Months with Possible extension

Terms: Contract W2


Description:

Onsite at the Thousand Oaks, CA facility not remote

M- F 6am-3pm (Morning), 2pm – 11pm (Swing), 10pm-7am (Night)

3 openings

1.5 years with possible extension of up to 3-year contract

Ideal candidate: They will be working on the manufacturing floor. Detail Oriented, Team player and Quality Experience.


Basic Qualifications:

Master degree OR Bachelor degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience

Ideal candidate: They will be working on the manufacturing floor. Detail Oriented, Team player and Quality Experience.


Top 3 Must Have Skill Sets:

Duties include but are not limited to:

Purposeful presence on the manufacturing floor, inc. Inspection support, ASP and QA assessments,

Electronic batch record review,

SOP revision approval,

Maximo System - Work order, job plan approvals,

Quality support and approval of minor deviations and CAPA records.

MES revisions and approvals


Day to Day Responsibilities:

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.

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