Repligen
QC Inspector
Repligen, Clifton Park, New York, United States, 12065
Overview:
This position will be responsible for inspecting products against the accept/reject criteria and assisting manufacturing with identifying and solving issues relating to rejects. The work environment is an ISO 7 cleanroom and requires gowning.Responsibilities:Interpret specifications and engineering drawings, inspect in-process and finished goods to these specificationsUse measurement tools such as calipers and gin gauges to perform dimensional inspections of goodsCommunicate any out of specification parts to operations/engineering and assist with root cause analysisPerform environmental monitoring of the ISO cleanroomsPerform incoming inspection on raw materials and accept/reject the material according to specificationsResponsible for area cleanliness, ambassador for contamination control in the ISO spacesUse Microsoft Office Suite programs to log and communicate results and nonconformitiesAssist with customer complaint investigationsCarry out required QC inspections during equipment and product validationsMay participate in internal audits of the Quality Management SystemQualifications:
HS Diploma or equivalent requiredBachelors degree in a science or relevant experience preferredMinimum of 2 years prior relevant experience preferredEffective and concise communication skills verbal and writtenAbility to use testing equipment and supplies accurately and efficientlyPrevious experience working within a cleanroom environment preferredMedical devices or medical manufacturing experience is highly desired
This position will be responsible for inspecting products against the accept/reject criteria and assisting manufacturing with identifying and solving issues relating to rejects. The work environment is an ISO 7 cleanroom and requires gowning.Responsibilities:Interpret specifications and engineering drawings, inspect in-process and finished goods to these specificationsUse measurement tools such as calipers and gin gauges to perform dimensional inspections of goodsCommunicate any out of specification parts to operations/engineering and assist with root cause analysisPerform environmental monitoring of the ISO cleanroomsPerform incoming inspection on raw materials and accept/reject the material according to specificationsResponsible for area cleanliness, ambassador for contamination control in the ISO spacesUse Microsoft Office Suite programs to log and communicate results and nonconformitiesAssist with customer complaint investigationsCarry out required QC inspections during equipment and product validationsMay participate in internal audits of the Quality Management SystemQualifications:
HS Diploma or equivalent requiredBachelors degree in a science or relevant experience preferredMinimum of 2 years prior relevant experience preferredEffective and concise communication skills verbal and writtenAbility to use testing equipment and supplies accurately and efficientlyPrevious experience working within a cleanroom environment preferredMedical devices or medical manufacturing experience is highly desired