Source description
About the role
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QA Specialist
- Cambridge, MA
- Full-time
Company Description
IRI believes in commitment, Integrity and strategic workforce solutions.
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.
Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.
Job Description
Job description
Perform the QA review/approval of analytical documentation:
Analytical method validation protocols and reports for in-process and release/stability testing
Analytical method procedures and associated change controls
Method technical transfer protocols and reports
Reference Standard and Critical Reagent qualification protocols and reports
Certificates of Analysis for reference materials and critical reagents
Standard Operating Procedures and other guidance documents
Collaborate with clinical or commercial analytical functions to determine the appropriate resolutions or CAPAs for protocol deviations/exceptional conditions related to method validations, technical transfers or reference standard/critical reagent qualifications
Collaborate with manufacturing support functions to develop the methods and acceptance criteria for the development of raw material specifications in preparation for Process Performance Qualification activities
Broad compliance knowledge (cGMP, ICH, FDA/EU guidance, WHO) as it applies to the evaluation of technical documents for analytical methods and reference materials
Experience with the review and approval of method validation protocols and reports
Experience collaborating with technical teams to develop validation strategies that are compliant to regulatory guidance and BMS policies
Experience collaborating with technical subject matter experts to resolve validation protocol or report compliance gaps and indicate if technical gaps are present with the overall validation strategy
Experience collaborating with technical subject matter experts to resolve protocol deviations and investigations
Additional Information
Regards,
Indu Dubey
Clinical Recruiter
732-844-8725
indu @irionline.com
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QA Specialist
- Cambridge, MA
- Full-time
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