Incoming Quality Assurance Specialist
Bloomsbury, NJ Bloomsbury, NJ Full-time Full-time Estimated:
$57.
1K - $72.
3K a year Estimated:
$57.
1K - $72.
3K a year Responsibilities may include:
Disposition steps in ERP system Assess critical data on released items in ERP system Release/Disposition of raw materials, sterile supplies, and labels Inspection of bulk bags from other QuVa sites Assist with the Coordination of transfers between QuVa Sites Incoming Environmental plate sampling or sending for testing Quality inspection and disposition in ERP of labels Manages In Process QC Supplier Ready for Receiver reports Quality inspections verification raw materials, sterile supplies Initiate DMI/DMR of non-conforming material Quality review / verification of critical information related to the receipt of incoming materials Escalate any discrepancies or non-conformances found during incoming receipt inspection Retrieves / requests quality documents (CoA, CoC, CoS) from vendors for incoming materials Ensures compliance of incoming materials prior to use in Manufacturing Operations Ensures company compliance to QuVa Pharma's Standard Operating Procedures (SOPs) and Quality Management System (QMS) Follows all regulatory guidelines, cGMP guidelines as required by the job function Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs Other duties as designated by Quality Management Other duties as assigned Experience Required At least 2 years' experience in FDA regulated Quality Assurance, Sterile Compounding and/or GMP production facility required Legally authorized to work in the job posting country Preferred 2 years' QuVa Pharma Quality Assurance Technician preferred Bachelor's Degree in life science or equivalent work experience preferred Education Required High School or better.
Estimated Salary: $20 to $28 per hour based on qualifications.
$57.
1K - $72.
3K a year Estimated:
$57.
1K - $72.
3K a year Responsibilities may include:
Disposition steps in ERP system Assess critical data on released items in ERP system Release/Disposition of raw materials, sterile supplies, and labels Inspection of bulk bags from other QuVa sites Assist with the Coordination of transfers between QuVa Sites Incoming Environmental plate sampling or sending for testing Quality inspection and disposition in ERP of labels Manages In Process QC Supplier Ready for Receiver reports Quality inspections verification raw materials, sterile supplies Initiate DMI/DMR of non-conforming material Quality review / verification of critical information related to the receipt of incoming materials Escalate any discrepancies or non-conformances found during incoming receipt inspection Retrieves / requests quality documents (CoA, CoC, CoS) from vendors for incoming materials Ensures compliance of incoming materials prior to use in Manufacturing Operations Ensures company compliance to QuVa Pharma's Standard Operating Procedures (SOPs) and Quality Management System (QMS) Follows all regulatory guidelines, cGMP guidelines as required by the job function Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs Other duties as designated by Quality Management Other duties as assigned Experience Required At least 2 years' experience in FDA regulated Quality Assurance, Sterile Compounding and/or GMP production facility required Legally authorized to work in the job posting country Preferred 2 years' QuVa Pharma Quality Assurance Technician preferred Bachelor's Degree in life science or equivalent work experience preferred Education Required High School or better.
Estimated Salary: $20 to $28 per hour based on qualifications.
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