Quality Control Analyst
The QC IT Application Analyst collaborates with the business and IT teams to provide
project support for MA Biologics Operations Site Functions Quality, Validation and Product Development.
The QC IT Application Analyst manages their work with limited oversight-
The scope of work includes, but is not limited to the following:
Project upgrades from win 7- win 10
Provide oversight of vendor-provided solutions
Handle ad-hoc technical requests from both internal and external partners in
accordance with projects that are assigned.
Work with other Direct team members for descions, and clariffications as needed
Must be able to juggle multiple projects and deliverables, and split billing time between projects where needed.
Experience with performing design testing of application to help author SDLC documents, including SDCS, URS, FRA, Admin Sop, IQ, IOQ, ATR, Application Data Flow diagrams, etc.
Must poses GXP experience with lab equipment.
Recommended Experience
Service now, Veeva, Trackwise, Active Directory, firewall rules, My Access, NTFS permissions. Excellent written and verbal communication.
Applications impacted by upgrades, Idele candidate should have previous experience
implementing, and or upgrading. Other application experience can be considered.
Vaya Raman
7500 Fast PCR
Hiac Particle Counters
Maldi-tof
Vi-Cell Cell counter
Antaris II
Waters Andrew + Alliance
Education and Experience Requirements
More than 5 years relevant IT/business experience, analysis, and documentation of business and technical requirements (required)
Experience with software application implementations in GxP environment (required)
Bachelor's degree or equivalent in information technology, computer science, engineering, or business administration,
Experience in the Pharmaceuticals or Life Sciences industry (preferred)
Experience consulting or working in a complex, global matrix organization (preferred)
Knowledge of Lean operational techniques (preferred)
Key Skills, Abilities, and Competencies
IT Technology Skills & Competencies
IT Experience deploying and supporting Quality and Manufacturing Systems
including Analytical Instruments Empower, Chromeleon, SOLO VPE, GE Unicorn, Nova Biomedical Bioprofile CDV and Flex2, Roche Cedex, Roche LightCycler 480, FileMaker Pro, Bartender, Charles River EndoScan-V, GE DataPro2, Informait InForm/CC, Lonza WinKQCL, Mettler Toledo LabX, PerkinElmer Asset Genius, Thermo WebAdmin for TruScan RM Analyzer, and various Laboratory desktop applications used in GxP environment
Familiarity with Automation systems such as SCADAs, PLCs, DCS, BAS, Historians
Experience with Computerized Systems Validation (CSV), 21 CFR Part 11 regulations, and Data Integrity compliance
Experience working with ITIL processes in ServiceNow such as Incident Management, Change Management, Problem Management, Asset and Configuration Management (CMDB)
Familiarity with following tools and processes TrackWise CAPA, Deviation, Change Control, Veeva Document Workflows
Familiarity with Operational Excellence and/or Continuous Improvement processes
Knowledge and familiarity of following Tools and technologies MS Office 365, MS Visio, MS Project
Citrix, Windows Desktop, Windows Server, SQL Databases, LDAP, Group Policy, TCP/IP Networks, Server Virtualization, RDP, Backup and Restore
Architectures 2 Tier, 3 Tier, On-premise, Cloud may be used in the QC / Manufacturing environment.
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
Dice Id:
80168598
Position Id:
8668557
The QC IT Application Analyst collaborates with the business and IT teams to provide
project support for MA Biologics Operations Site Functions Quality, Validation and Product Development.
The QC IT Application Analyst manages their work with limited oversight-
The scope of work includes, but is not limited to the following:
Project upgrades from win 7- win 10
Provide oversight of vendor-provided solutions
Handle ad-hoc technical requests from both internal and external partners in
accordance with projects that are assigned.
Work with other Direct team members for descions, and clariffications as needed
Must be able to juggle multiple projects and deliverables, and split billing time between projects where needed.
Experience with performing design testing of application to help author SDLC documents, including SDCS, URS, FRA, Admin Sop, IQ, IOQ, ATR, Application Data Flow diagrams, etc.
Must poses GXP experience with lab equipment.
Recommended Experience
Service now, Veeva, Trackwise, Active Directory, firewall rules, My Access, NTFS permissions. Excellent written and verbal communication.
Applications impacted by upgrades, Idele candidate should have previous experience
implementing, and or upgrading. Other application experience can be considered.
Vaya Raman
7500 Fast PCR
Hiac Particle Counters
Maldi-tof
Vi-Cell Cell counter
Antaris II
Waters Andrew + Alliance
Education and Experience Requirements
More than 5 years relevant IT/business experience, analysis, and documentation of business and technical requirements (required)
Experience with software application implementations in GxP environment (required)
Bachelor's degree or equivalent in information technology, computer science, engineering, or business administration,
Experience in the Pharmaceuticals or Life Sciences industry (preferred)
Experience consulting or working in a complex, global matrix organization (preferred)
Knowledge of Lean operational techniques (preferred)
Key Skills, Abilities, and Competencies
IT Technology Skills & Competencies
IT Experience deploying and supporting Quality and Manufacturing Systems
including Analytical Instruments Empower, Chromeleon, SOLO VPE, GE Unicorn, Nova Biomedical Bioprofile CDV and Flex2, Roche Cedex, Roche LightCycler 480, FileMaker Pro, Bartender, Charles River EndoScan-V, GE DataPro2, Informait InForm/CC, Lonza WinKQCL, Mettler Toledo LabX, PerkinElmer Asset Genius, Thermo WebAdmin for TruScan RM Analyzer, and various Laboratory desktop applications used in GxP environment
Familiarity with Automation systems such as SCADAs, PLCs, DCS, BAS, Historians
Experience with Computerized Systems Validation (CSV), 21 CFR Part 11 regulations, and Data Integrity compliance
Experience working with ITIL processes in ServiceNow such as Incident Management, Change Management, Problem Management, Asset and Configuration Management (CMDB)
Familiarity with following tools and processes TrackWise CAPA, Deviation, Change Control, Veeva Document Workflows
Familiarity with Operational Excellence and/or Continuous Improvement processes
Knowledge and familiarity of following Tools and technologies MS Office 365, MS Visio, MS Project
Citrix, Windows Desktop, Windows Server, SQL Databases, LDAP, Group Policy, TCP/IP Networks, Server Virtualization, RDP, Backup and Restore
Architectures 2 Tier, 3 Tier, On-premise, Cloud may be used in the QC / Manufacturing environment.
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
Dice Id:
80168598
Position Id:
8668557
Job ID: 481237843
Originally Posted on: 6/14/2025
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