QA Associate II
Company: Joul--
Location: Mahwah
Posted on: May 4, 2025
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Job Description:
Job Title: Quality Assurance Associate II
Do you have the right skills and experience for this role Read on
to find out, and make your application.
Location: Mahwah, NJ area
Schedule: Tues- Saturday 2nd shift 4 PM- 12:30 AM (some flex
needed)
Type: Contract to Hire
Must Haves: BS or higher education degree in a scientifically
related field
Experience in a biologics or biotechnology company (1-3 years)
Working knowledge and technical understanding of the aseptic
manufacture of biologics preferred
Experience with batch record review in a biotechnology
manufacturing environment.
Experience reviewing QC data in a biotechnology manufacturing
environment
Working knowledge of GMP and TCTP regulations
Experience in reviewing GMP/GCTP related documents
(validations/qualifications reports, SOPs, etc)
Responsibilities: Under direct supervision, the associate supports
daily tasks that are essential for maintaining and improving
quality systems and adhering to client-specific procedures.
Key responsibilities include document management, review of
manufacturing batch records, quality control (QC) data,
facilitating material releases, overseeing final product releases,
and providing essential assistance to the Quality Management as
needed.
Ensures that all procedures and processes meet internal quality
standards as well as external regulations specific to pre-clinical,
clinical and commercial manufacturing.
Read, understand and follow all cGMP and cGTP documentation for
Quality System Functions (SOPs,WIs,etc.)
Maintain cGMP and cGTP compliance for all aspects of pre-clinical,
clinical and commercial manufacturing.
Release raw material in ERP system as well as on paper.
Perform Accessioning of incoming Apheresis.
Review Batch record and disposition material of finished product to
client.
Provides information for Out of Specification and deviations to
investigator.
Performs line clearance prior to manufacturing operations
begins.
Supports tech transfer activities.
Other duties as assigned.
Build Quality into all aspects of your work by maintaining
compliance to all quality requirements.
Ensure compliance to all FDA and Worldwide Quality & Compliance
regulations (As applicable to the job function).
Attend all required Quality & Compliance training at the specified
interval.
Benefits
System One offers eligible employees health and welfare benefits
coverage options, including medical, dental, vision, spending
accounts, life insurance, voluntary plans, and participation in a
401(k) plan.
Ref: #558-Scientific
Keywords: Joul--, Hoboken , QA Associate II, Other , Mahwah, New Jersey
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here to apply!
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