ISEE Careers
Document Controller
ISEE Careers, New Brunswick, New Jersey, us, 08933
About the job Document Controller
Company Overview
The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests.
Responsibilities
Develop and implement production processes related to document control and managementCollect and register all technical document, such as drawings and blueprints in the Companys systemReview and update documents for maintenance and quality controlKeep other personnel updated on new document versions and how to obtain accessHandle records across various departmentsCreate templates for use by other personnelMaintain confidentiality regarding sensitive documentsEstablish and maintain record-retention timelinesGenerate and/or revise SOPs, QF, and QOP used for the Production TeamRespond and communicate with all levels of production personnel, as well as other departments regarding documents and their controlCorrespond with and coordinate all activities related to documentsManage new machine validation procedures, including reviewing the validation protocols and generated dataRequirements
BA or BS degrees, or an equivalentBilingual (Korean and English)Strong communication skills with supervisors and other department personnelUnderstand production process linesAbility to generate product-related documents effectivelyHaving good knowledge and training in GMP/QMS is a mustBenefits
Health, Dental & VisionPTO401(k)IncentivesRelocation Assistance
Company Overview
The Company develops, manufactures, and markets in-vitro diagnostics (IVD) tests.
Responsibilities
Develop and implement production processes related to document control and managementCollect and register all technical document, such as drawings and blueprints in the Companys systemReview and update documents for maintenance and quality controlKeep other personnel updated on new document versions and how to obtain accessHandle records across various departmentsCreate templates for use by other personnelMaintain confidentiality regarding sensitive documentsEstablish and maintain record-retention timelinesGenerate and/or revise SOPs, QF, and QOP used for the Production TeamRespond and communicate with all levels of production personnel, as well as other departments regarding documents and their controlCorrespond with and coordinate all activities related to documentsManage new machine validation procedures, including reviewing the validation protocols and generated dataRequirements
BA or BS degrees, or an equivalentBilingual (Korean and English)Strong communication skills with supervisors and other department personnelUnderstand production process linesAbility to generate product-related documents effectivelyHaving good knowledge and training in GMP/QMS is a mustBenefits
Health, Dental & VisionPTO401(k)IncentivesRelocation Assistance