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AMPAC Fine Chemicals
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AMPAC Fine Chemicals
Posted 3 months ago
Full Time
Rancho Cordova, California
In Person
Smart Summary
Responsibilities
The Quality Assurance Specialist I supports quality systems, coordinates cross-functional IPT meetings, and manages the release of pharmaceutical products. Key duties include conducting investigations for deviations, managing change controls, and performing facility audits to ensure GMP compliance.
Qualifications
You have an Associate's degree and 0-2 years of related technical experience in the pharmaceutical industry. You will be responsible for supporting quality systems, ensuring GMP compliance, and managing batch release processes. Strong attention to detail and the ability to work in a fast-paced, team-oriented environment are crucial.
Must Have Skills for ATS
cGMP
GMP production
document control
production record review
process validation
qualification protocols
facility audits
investigations
batch release
change controls
VAR
MNCRs
OOS/OOT investigations
QCRs
Job Description
We are looking for enthusiastic Quality Professionals to join our Quality Assurance Team! We have opportunities at our Rancho Cordova, CA (greater Sacramento area).
Job Summary:
Quality Assurance Specialist I is responsible for supporting multiple programs or supporting the coordination of the quality systems, but not necessarily both. The Quality Assurance Specialist I will be responsible for ensuring that adequate QA support is provided for the cross functional IPT meetings and customer teleconferences. Work is closely supervised.
Duties and Responsibilities:
Responsible for communicating the status of QA related items to the IPT Team including batch release and investigation status
Take an active role providing, as appropriate, guidance within the approved systems and procedures as it related to GMP production and release of products, some of this guidance may be required outside of the typical working schedule (off shift)
Responsible for taking an active role in planning and execution of action items related to support of production and product release, including document control and production record review activities.
Responsible for managing the release of products to support subsequent production and release of product to customer within the approved systems and procedures
Responsible for managing change controls in support of production and release activities
Responsible for review and/or conduct of investigations for deviations in production and testing (VAR, MNCRs, OOS/OOT investigations, QCRs)
Responsible for ensuring process validation and qualification requirements are established in approved protocols and results of the validation and qualifications are adequately presented in approved reports. Responsible for facility audits of the respective manufacturing facilities at the start of each campaign and periodically while long running campaigns are active.
Responsible for ensuring that reports within a given system are progressing in a manner that complies with the approved procedures and deadlines
Responsible for ensuring submitted reports contain adequate information and attachments/links to allow appropriate review and approval
Responsible for assignment and/or reassignment of appropriate personnel to the documentation, review and approval of quality systems reports
Responsible for the development and reporting of appropriate metrics for review by management and to obtain and maintain appropriate training for the requirements of this role
EDUCATION AND EXPERIENCE
COMPETENCIES/SKILLS
CERTIFICATIONS and LICENSES
This job description does not constitute a contract of employment or otherwise limit employment-at-will rights at any time
SKPT offers competitive salaries, benefits, and matching 401k. Our Company is an Equal Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender expression or identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics, both state and federal.
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AMPAC Fine Chemicals
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