MCS Senior Associate Quality Assurance
Aequor JD ·www.aequor.com
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FULLY ONSITE AT USTO
Must be flexible as it is possible worker will start on any shift. Rotate every 6 months.
Day 6am-5pm
Swing's 1pm-(12am)
Graves 7pm-8am
Will change on the business they are supporting
Rotate every 6 months
The manager is seeking a Senior Associate, Quality Assurance (MCS) to provide real-time, floor-based QA support at *** s USTO site. This fully onsite role involves rotating between day and swing shifts every six months, beginning on day shift for training. The position supports Clinical/Commercial drug substance production and requires cleanroom oversight, batch record review, and acting as a QA liaison during manufacturing and facility events. Ideal candidates will have hands-on QA or manufacturing experience in a GMP environment (preferably within biotech or ***) with strong critical thinking skills prioritized over academic credentials. A bachelor's degree in Biochemistry, Biology, Chemistry, or related scientific disciplines is preferred but not required. The manager is open to training strong candidates but will not consider those who are purely academic or significantly overqualified without clear justification.
This position supports *** s Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Substance manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering areas/staff in the execution of their processes, procedures, and use of quality systems. Duties include purposeful presence on the floor, electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations . 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 for the Drug Substance 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.
Also, ability to make Quality based decisions in order to ensure compliance.
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.
Must be flexible as it is possible worker will start on any shift. Rotate every 6 months.
Day 6am-5pm
Swing's 1pm-(12am)
Graves 7pm-8am
Will change on the business they are supporting
Rotate every 6 months
The manager is seeking a Senior Associate, Quality Assurance (MCS) to provide real-time, floor-based QA support at *** s USTO site. This fully onsite role involves rotating between day and swing shifts every six months, beginning on day shift for training. The position supports Clinical/Commercial drug substance production and requires cleanroom oversight, batch record review, and acting as a QA liaison during manufacturing and facility events. Ideal candidates will have hands-on QA or manufacturing experience in a GMP environment (preferably within biotech or ***) with strong critical thinking skills prioritized over academic credentials. A bachelor's degree in Biochemistry, Biology, Chemistry, or related scientific disciplines is preferred but not required. The manager is open to training strong candidates but will not consider those who are purely academic or significantly overqualified without clear justification.
This position supports *** s Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Substance manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities & Engineering areas/staff in the execution of their processes, procedures, and use of quality systems. Duties include purposeful presence on the floor, electronic batch record review, SOP revision & approval, work order approval, and quality approval of minor deviations . 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 for the Drug Substance 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.
Also, ability to make Quality based decisions in order to ensure compliance.
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.
Frequently asked questions
Who is hiring for the MCS Senior Associate Quality Assurance role?
Aequor JD is hiring for the MCS Senior Associate Quality Assurance position, a Shazamme client. Apply directly on the employer's career site.
Where is the MCS Senior Associate Quality Assurance job located?
The MCS Senior Associate Quality Assurance role with Aequor JD is based in Thousand Oaks, CA, US. The role is hybrid-friendly.
Is the MCS Senior Associate Quality Assurance role remote?
Yes — the MCS Senior Associate Quality Assurance position at Aequor JD is hybrid. Candidates based in US are preferred.
Is the MCS Senior Associate Quality Assurance role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the MCS Senior Associate Quality Assurance role?
The MCS Senior Associate Quality Assurance position is aimed at senior-level candidates.
How do I apply for the MCS Senior Associate Quality Assurance role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.