Quality Control Analyst

Overview

Hybrid
$90 - $100
Contract - W2
Contract - 12 Month(s)

Skills

Quality Control
GxP
Product Development
Information Technology

Job Details

  • 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.

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