QC Information Services Analyst (GMP, LIMS, IT Support) - LG
Salary undisclosed
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Description:
Job title: Senior QCISO Analyst
Location: Fredrick, MD - 100% onsite
Working Hours- M-F 8am-4pm or 9am-5pm
Typical day will include project work, password resets, user access requests, software troubling shooting, make restricted folders for users, writing SOPs, executing text scripts.
Manager is looking for Software IT experience including software configuration and user management.
As a QC Information Systems (QCIS) Specialist, you will act as an administrator of computerized systems and business analyst between labs groups and IT for Enterprise projects such as Empower, Biovia Laboratory Execution Systems (LES), Labware, LIMS, and other digital initiatives. Candidates should have a technical understanding of GMP analytical laboratory Information and Enterprise systems. Responsible for day-to-day job functions, administration tasks and can independently represent the team for site and global initiatives.
Perform day-to-day activities and application administration of lab and manufacturing quality control computerized systems.
Support QC lab functions, providing solutions to a variety of technical problems.
Participate in software/computer system validation, IT for software/computer applications and fulfill all networking and security requirements, and global IT for enterprise software applications.
Facilitate and coordinate training of new and existing local admins, prepare training materials as necessary.
Executes protocols, reports, investigations using, and other records, using Veeva on behalf of QC.
Support QC information system lifecycle management activities from concept, development, validation, implementation, maintenance, to retirement.
Ability to interpret scientific documentation (quality assay SOPs, Master Specifications, etc.) in order to translate information into static data configuration and reports in LIMS, Empower, and other computerized data management systems, is a plus for some roles within the team.
Education:
Bachelor's Degree preferably in Information Systems/Technology or Biotechnology related field.
0-3+ years information management experience is preferred. Experience in a scientific lab setting a plus.
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Additional Details
- Does the position allow for the worker to be virtual/remote? : No
- Critical Position? : No
- Career Level : D
- External Job Title : (No Value)
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job Description:
Job title: Senior QCISO Analyst
Location: Fredrick, MD - 100% onsite
Working Hours- M-F 8am-4pm or 9am-5pm
Typical day will include project work, password resets, user access requests, software troubling shooting, make restricted folders for users, writing SOPs, executing text scripts.
Manager is looking for Software IT experience including software configuration and user management.
As a QC Information Systems (QCIS) Specialist, you will act as an administrator of computerized systems and business analyst between labs groups and IT for Enterprise projects such as Empower, Biovia Laboratory Execution Systems (LES), Labware, LIMS, and other digital initiatives. Candidates should have a technical understanding of GMP analytical laboratory Information and Enterprise systems. Responsible for day-to-day job functions, administration tasks and can independently represent the team for site and global initiatives.
Perform day-to-day activities and application administration of lab and manufacturing quality control computerized systems.
Support QC lab functions, providing solutions to a variety of technical problems.
Participate in software/computer system validation, IT for software/computer applications and fulfill all networking and security requirements, and global IT for enterprise software applications.
Facilitate and coordinate training of new and existing local admins, prepare training materials as necessary.
Executes protocols, reports, investigations using, and other records, using Veeva on behalf of QC.
Support QC information system lifecycle management activities from concept, development, validation, implementation, maintenance, to retirement.
Ability to interpret scientific documentation (quality assay SOPs, Master Specifications, etc.) in order to translate information into static data configuration and reports in LIMS, Empower, and other computerized data management systems, is a plus for some roles within the team.
Education:
Bachelor's Degree preferably in Information Systems/Technology or Biotechnology related field.
0-3+ years information management experience is preferred. Experience in a scientific lab setting a plus.
| External Job Title try { var fgTooltip = new FG.Tooltip({ element: $('#cf_descz'), text: "This\x20title\x20is\x20known\x20in\x20the\x20market\x20place\x20and\x20will\x20help\x20suppliers\x20source\x2Frecruit\x20potential\x20candidates" }).initialize(); } catch(err) {} |
Additional Details
- Does the position allow for the worker to be virtual/remote? : No
- Critical Position? : No
- Career Level : D
- External Job Title : (No Value)
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job