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MCS Senior Associate Quality Assurance

Company: Aditi Consulting
Location: Newbury Park
Posted on: April 6, 2025

Job Description:

Payrate: $ 30.00- $ 32.00/hr.

Learn more about the general tasks related to this opportunity below, as well as required skills.



Summary:

The Sr. Associate Quality Assurance 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 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



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



Top 3 Must Have Skill Sets:

Detail Oriented
Team player
Quality Assurance Experience.



Day to Day Responsibilities:

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.



Pay Transparency:

The typical base pay for this role across the U.S. is: $ 30.00- $ 32.00/hr.. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.



For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our Privacy Policy (https://www.aditiconsulting.com/privacy-policy).



Aditi Consulting LLC uses AI technology to engage candidates during the sourcing process. AI technology is used to gather data only and does not replace human-based decision making in employment decisions. By applying to this position, you agree to Aditi's use of AI technology including calls from an AI Voice Recruiter.



#AditiConsulting

Keywords: Aditi Consulting, Los Angeles , MCS Senior Associate Quality Assurance, Other , Newbury Park, California

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