Senior Associate Quality Assurance

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Senior Associate Quality Assurance

Contract: Thousand Oaks, California, US

Salary: $33.00 Per Hour

Job Code: 347597

End Date: 2024-04-30
Days Left: 10 days, 3 hours left

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To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - https://www.linkedin.com/in/chitrank-rastogi-55119a102/), email your updated resume at Email - [email protected] or give me a call at (425) 523-1648. Thank you!

Pay Range - $30 to $33/hr. (negotiable)

Job Description:
Job Roles & Responsibilities:
This position supports our 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 and CAPA records.
Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion.
The Sr. Associate will also represent a 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, the ability to make Quality-based decisions 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.
Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
Top 3 Must Have Skill Sets: Experience working with Quality Systems / QA
Batch Record Experience
Plant Quality Assurance provides quality oversight to manufacturing
Looking for someone who can work cross-functionally amongst many different teams and be comfortable with shifting priorities as the business needs change.
Day to Day Responsibilities: Duties include electronic batch record review, batch record review, SOP and MP revision approval, work order approval, and quality approval of non-conformances and CAPAs.
Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion.
The incumbent will also represent functional area quality for the Bulk Quality Assurance department in the execution of projects necessary to achieve departmental operational excellence goals and will work in a team matrix environment.
Job Requirement Quality Assurance Associate
Biochemistry
Biology
Chemistry
CAPAs
Quality Systems
batch record
SOP
Quality Assurance
electronic batch record
compliance
Biotech
Biotechnology
Pharma
Pharmaceuticals
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Recruiter
Email
Phone
Chitrank Rastogi
[email protected]

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