Overview

Quality Assurance Senior Associate Jobs in Thousand Oaks, CA at SPECTRAFORCE

Title: Quality Assurance Senior Associate

Company: SPECTRAFORCE

Location: Thousand Oaks, CA

Job Title: Quality Assurance Senior Associate

Location: Thousand Oaks, CA, 91320

Duration: 18 months

Description:

Onsite at the Thousand Oaks, CA facility not remote

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

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.

The Sr. Associate Quality Assurance position supports Client’s 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 and Engineering staff in the execution of their processes, procedures, and use of quality systems.

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

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.

Ability to evaluate 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

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