We apologize for the inconvenience but the job you are looking for has been filled or it has been removed by the recruiter. For your reference, the original listing is shown at the bottom of this page.
Listed below are the top 10 out of 23 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Pearl River, NY
Lead internal quality management system audits to 21CFR 820, ISO 13485:2003, 93/42/EEC and other applicable Standards to determine whether the quality management ...
This position is responsible for conducting internal and external GCP/GLP Compliance auditing activities. * Conducts document reviews/audits of informed consents, ...
A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. A global ...
Lead internal and external GCP/GLP Compliance auditing activities inclusive of due diligence and system audits. Provide GCP/GLP Compliance leadership to quality ...
Cornerstone Search Group, LLC - New York City, NY US
Global Quality Assurance (QA) Leader: Growing Biotech, New York City area Summary: Our client is a highly attractive and innovative globally traded Biotech ...
1) Independently leads the QA input to validation projects in support of commercial manufacturing. 2) Review/Audit batch records. Provides input into strategy ...
control/Quality assurance (QA/QC) function for The... Desired Qualifications: . Lead Auditor . IRCA or Equivalent Lead Auditor Certification Preferred......
For your reference, we have included the original job posting below.
QA Auditor
Job Number:
43301899
Company Name:
Sunrise Systems Inc
Job Location:
Pearl River, NY US
Job Category:
Science & Biotech
QA Auditor
1) Independently leads the QA input to validation projects in support of commercial manufacturing. 2) Review/Audit batch records. Provides input into strategy and direction to project teams on compliance/technical issues related to validation efforts to achieve compliance with company policies and government regulations. Reviews and approves validation documentation including specifications, protocols and reports with a focus on cGMP impact and validation lifecycle requirements. Independently re...
