MCS Senior Associate Quality Assurance
Company: Aditi Consulting
Location: Newbury Park
Posted on: April 6, 2025
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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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