Alphanumeric Systems Canada Ltd
Facilities Engineering Technical/Deviation Writer 2410424101
Alphanumeric Systems Canada Ltd, Cambridge, Massachusetts, us, 02140
Alphanumeric is hiring a
FACILITIES ENGINEERING TECHNICAL/DEVIATION WRITER
to work in Cambridge, MA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.
Learn more about the general tasks related to this opportunity below, as well as required skills.The Tech Writer is responsible for performing GxP investigation activities and owning and authoring deviation investigation reports for the FEV (Facilities, Engineering and Validation) department, as well as revising and writing procedures, and acting as document coordinator.Primary Responsibilities:
Update, author and review FEV standard operating procedures and other controlled documents as a result of process improvements and CAPAs, Gap Assessments.Perform investigation activities and writing deviation investigation reports for FEV departments.Collaborate with SMEs from other departments to ensure a cross-functional evaluation is completed and ensure alignment of GxP practices.Coordinate prompt event evaluation, investigation, closure and follow-up of process/equipment discrepancies and related areas as well as identify opportunities for continuous process improvements.Write concise and accurate investigation reports.Utilize various root cause analysis, analytical and problem-solving tools to determine root cause of GxP deviations and assist with the completion of impact analysis and identification of appropriate corrective actions to prevent recurrence.Participate in determining the appropriate corrective and preventative actions (CAPAs) after the investigation process.Initiate Change Controls as required for Engineering/Facilities operations.Manage Facilities Engineering GMP documents through lifecycle as document coordinator.Education and Experience:
Requires a bachelor's degree, preferably in a scientific/engineering discipline, with a minimum of 3-5 years of experience in a pharmaceutical or related industry.Demonstrate a sound understanding of cGMP's, FDA regulations, and pharmaceutical manufacturing/packaging processes.Minimum of 3 years technical experience in a regulated GxP environment.Experience in troubleshooting, investigation, and root-cause/analytical/problem-solving for equipment related issues.Demonstrated, strong technical writing skills with the ability to read, comprehend, and communicate complex, technical events in a manner that is concise, clear, and accurate.Demonstrated ability to work independently and as part of a collaborative, cross-functional team.Working knowledge of SAP or similar deviation management system, and Veeva or similar quality document system.
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FACILITIES ENGINEERING TECHNICAL/DEVIATION WRITER
to work in Cambridge, MA with our client of 20 years committed to improving lives through medical and pharmaceutical advancements.
Learn more about the general tasks related to this opportunity below, as well as required skills.The Tech Writer is responsible for performing GxP investigation activities and owning and authoring deviation investigation reports for the FEV (Facilities, Engineering and Validation) department, as well as revising and writing procedures, and acting as document coordinator.Primary Responsibilities:
Update, author and review FEV standard operating procedures and other controlled documents as a result of process improvements and CAPAs, Gap Assessments.Perform investigation activities and writing deviation investigation reports for FEV departments.Collaborate with SMEs from other departments to ensure a cross-functional evaluation is completed and ensure alignment of GxP practices.Coordinate prompt event evaluation, investigation, closure and follow-up of process/equipment discrepancies and related areas as well as identify opportunities for continuous process improvements.Write concise and accurate investigation reports.Utilize various root cause analysis, analytical and problem-solving tools to determine root cause of GxP deviations and assist with the completion of impact analysis and identification of appropriate corrective actions to prevent recurrence.Participate in determining the appropriate corrective and preventative actions (CAPAs) after the investigation process.Initiate Change Controls as required for Engineering/Facilities operations.Manage Facilities Engineering GMP documents through lifecycle as document coordinator.Education and Experience:
Requires a bachelor's degree, preferably in a scientific/engineering discipline, with a minimum of 3-5 years of experience in a pharmaceutical or related industry.Demonstrate a sound understanding of cGMP's, FDA regulations, and pharmaceutical manufacturing/packaging processes.Minimum of 3 years technical experience in a regulated GxP environment.Experience in troubleshooting, investigation, and root-cause/analytical/problem-solving for equipment related issues.Demonstrated, strong technical writing skills with the ability to read, comprehend, and communicate complex, technical events in a manner that is concise, clear, and accurate.Demonstrated ability to work independently and as part of a collaborative, cross-functional team.Working knowledge of SAP or similar deviation management system, and Veeva or similar quality document system.
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