Artech Information System LLC
QA Associate
Artech Information System LLC, Morris Plains, New Jersey, us, 07950
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description
The incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements.Coordinates and performs batch record issuance for internally manufactured products. Reviews and approves manufacturing and QC related documents for raw material disposition.Reviews and approves manufacturing and QC related documents for manufactured media. Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center. Supports cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance. Controls costs within department to meet budget.Completes job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements. Performs or supports any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.Qualifications
Skills:
0-3 years GMP manufacturing and/or QA related experienceEducation: BS/BA in Biological Sciences or equivalent relevant career experience
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The incumbent will have responsibility to ensure that all aspects of the operational business comply with cGMP legal and regulatory requirements, the Client Pharma Corporate Quality Manual and Policies, and site procedures and business requirements.Coordinates and performs batch record issuance for internally manufactured products. Reviews and approves manufacturing and QC related documents for raw material disposition.Reviews and approves manufacturing and QC related documents for manufactured media. Performs administrative functions for filing and maintenance of records between QA operations and Document Control Center. Supports cGMP and associated OJT training to QA and other departments to improve right the first time (RTFT), high quality performance. Controls costs within department to meet budget.Completes job-related training in electronic database system along with GMP, safety, and Ethics & Compliance course requirements. Performs or supports any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.Qualifications
Skills:
0-3 years GMP manufacturing and/or QA related experienceEducation: BS/BA in Biological Sciences or equivalent relevant career experience
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