Data Entry Operator

Company: ACS Solutions
Location: New Brunswick
Posted on: June 15, 2022

Job Description:

Data Entry Operator Location: New Brunswick, NJ Duration: 12 Months this is a hybrid role - 50% onsite Job Description: Responsible for collecting/monitoring End to End continuous process verification (CPV) data from multiple manufacturing nodes as required, performs statistical analysis/ trending of critical data, provides reports, prepares and presents analysis in robustness meetings. Support global and site investigation by collecting and analyzing data as required. Collects data from batch records, spreadsheets, SAP, LIMS etc. The data collection may span several products/product families and sites. At a regular/defined frequency (e.g. end of manufacturing campaigns), enters and maintains data in tracking spreadsheets, databases and support Spotfire metrics etc., Creates/ edits excel templates for data collection and analysis. Performs analysis and trending of batch data, specifically process control and capability charts. Provides reports / presentations on a routine basis and prepares CPV reports for APQRs. Maintain central repository of all data collection and reports. Effectively communicates and escalates issues as appropriate. Supports quality investigations with data and trending analysis. Responsible for personal, colleague, and workplace safety. Supports efforts to meet / exceed group and department objectives. Required skills and education: Bachelor's degree required, preferably in science, engineering, or other related technical discipline * Experience with MS office, especially Excel, Word, PowerPoint, MS project and statistical software JMP/Minitab. * 3-5 years of experience in pharmaceutical industry data management and analysis preferred. * Knowledge of solid oral dose manufacturing unit operations is required. * Excellent verbal, written, and interpersonal communication skills are essential. * Demonstrated ability to collect, communicate and present data and information. * Knowledge of statistics and ability to comprehend complex analysis is a plus. Prior experience in the pharmaceutical industry and general knowledge of manufacturing process is a plus Job Requirements:Data Entry Operator
Location: New Brunswick, NJ
Duration: 12 Months

this is a hybrid role - 50% onsite

Job Description:
Responsible for collecting/monitoring End to End continuous process verification (CPV) data from multiple manufacturing nodes as required, performs statistical analysis/ trending of critical data, provides reports, prepares and presents analysis in robustness meetings.
Support global and site investigation by collecting and analyzing data as required.
Collects data from batch records, spreadsheets, SAP, LIMS etc. The data collection may span several products/product families and sites.
At a regular/defined frequency (e.g. end of manufacturing campaigns), enters and maintains data in tracking spreadsheets, databases and support Spotfire metrics etc.,
Creates/ edits excel templates for data collection and analysis.
Performs analysis and trending of batch data, specifically process control and capability charts.
Provides reports / presentations on a routine basis and prepares CPV reports for APQRs.
Maintain central repository of all data collection and reports.
Effectively communicates and escalates issues as appropriate.
Supports quality investigations with data and trending analysis.
Responsible for personal, colleague, and workplace safety. Supports efforts to meet / exceed group and department objectives.

Required skills and education:
Bachelor's degree required, preferably in science, engineering, or other related technical discipline
--- Experience with MS office, especially Excel, Word, PowerPoint, MS project and statistical software JMP/Minitab.
--- 3-5 years of experience in pharmaceutical industry data management and analysis preferred.
--- Knowledge of solid oral dose manufacturing unit operations is required.
--- Excellent verbal, written, and interpersonal communication skills are essential.
--- Demonstrated ability to collect, communicate and present data and information.
--- Knowledge of statistics and ability to comprehend complex analysis is a plus.
Prior experience in the pharmaceutical industry and general knowledge of manufacturing process is a plus

Keywords: ACS Solutions, New Brunswick , Data Entry Operator, Other , New Brunswick, New Jersey