QC IT Application Analyst - GxP
Location: Lexington, MA - 5 days per week ONSITE
Overall:
We are looking for a candidate who can support QCIT operations in a GMP environment, including:
Developing and executing periodic validation activities (backup and restore testing, user access reviews, and audit trail reviews)
Front-line client support and triage (initial assessment and coordination of repair activities when systems are down)
Supporting GxP workstation patching activities
Supporting decommissioning activities (for example, final backups and account deactivations)
Job Description:
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 –
o TrackWise – CAPA, Deviation, Change Control
o Veeva – Document Workflows
Familiarity with Operational Excellence and/or Continuous Improvement processes
Knowledge and familiarity of following Tools and technologies
o MS Office 365, MS Visio, MS Project
o Citrix, Windows Desktop, Windows Server, SQL Databases, LDAP, Group Policy, TCP/IP Networks, Server Virtualization, RDP, Backup and Restore
o Architectures – 2 Tier, 3 Tier, On-premise, Cloud
Physical Demands:
Must be able to lift, push, pull and carry up to 30 lbs.
In general, the position requires a combination of sedentary work and walking around observing conditions in the facility.
Working Environment:
Must be able to work in controlled environments requiring special gowning. Will potentially be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.
No make-up, jewelry, contact lenses, nail polish or artificial fingernails, or any oral food, tabaco, candy etc. may be used in the QC / Manufacturing environment.
During onboarding and training Onsite requirement will be 5 days per week. Afterwards minimum 3-4 days a week onsite is required.
Must be able to work overtime as required.
May be required to work in a confined area
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