Quality Assurance Auditor - Madison, WI
Posted: 3/30/2005 11:44:35 AM
This job is closed
NDT.org Job Number:
9813
* Please reference NDT.org Job Number on all correspondence
Contact:
Mike Wilmarth
Company:
Work Wonders Staffing, LLC
State:
Wisconsin
Contact:
Mike Wilmarth
Country:
USA
Length:
Perm/Regular/Full-time
Quality Assurance Auditor - Madison, WI
I am assisting to recruit a QA Auditor for a specialty pharmaceutical company located near Madison, WI.
This company is a specialty pharmaceutical company engaged in the discovery, development and commercialization of innovative therapeutic products to treat the unmet medical needs of patients with debilitating conditions and life-threatening diseases.
Their current commercial and therapeutic focus is in nephrology, utilizing a novel vitamin D2 hormone therapy. In addition to chronic kidney disease, the Company is developing vitamin D hormone therapies to treat hyperproliferative disorders such as cancer and psoriasis.
This person will be responsible for conducting cGMP related audits for contract testing facilities, their internal laboratory and conducting 21 CFR Part 11 software and vendor audits. Other responsibilities include managing vendor audits and quality project activities, supporting quality investigations, deviations, and maintaining the appropriate SOP's and quality documentation.
This company offers a competitive salary (60 - 70K) and benefits package, a team oriented working environment, and strong potential for career growth for the right person. Relocation is fully paid.
If you are interested in pursuing this opportunity, please forward your resume, relocation considerations and salary requirement to resumes@workwondersstaffing.net.
I am assisting to recruit a QA Auditor for a specialty pharmaceutical company located near Madison, WI.
This company is a specialty pharmaceutical company engaged in the discovery, development and commercialization of innovative therapeutic products to treat the unmet medical needs of patients with debilitating conditions and life-threatening diseases.
Their current commercial and therapeutic focus is in nephrology, utilizing a novel vitamin D2 hormone therapy. In addition to chronic kidney disease, the Company is developing vitamin D hormone therapies to treat hyperproliferative disorders such as cancer and psoriasis.
This person will be responsible for conducting cGMP related audits for contract testing facilities, their internal laboratory and conducting 21 CFR Part 11 software and vendor audits. Other responsibilities include managing vendor audits and quality project activities, supporting quality investigations, deviations, and maintaining the appropriate SOP's and quality documentation.
This company offers a competitive salary (60 - 70K) and benefits package, a team oriented working environment, and strong potential for career growth for the right person. Relocation is fully paid.
If you are interested in pursuing this opportunity, please forward your resume, relocation considerations and salary requirement to resumes@workwondersstaffing.net.
Skills:
Candidate must possess a B.S./B.A. degree in biology, chemistry, or related field and have 4 + years of auditing, quality assurance or cGMP compliance related experience. Comprehensive knowledge and experience working under pharmaceutical manufacturing cGMP's, 21 CFR Part 11, GLP's, GCP's and ICH Clinical Guidelines preferred as well as excellent written and oral communication skills, ability to work independently, strong computer skills and the ability to travel.
