LanceSoft
QC IT Application Analyst
LanceSoft, Lexington, Massachusetts, United States, 02173
Shift: 8AM to 5PM
Onsite Expectations:
For onboarding and training for the first few weeks should plan to be onsite 4-5 days a week. After onboarding and started working on projects, it is a minimum 3 days a week onsite, there will be times to be on site 4-5 days as needed.
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 solutionsHandle ad-hoc technical requests from both internal and external partners in accordance with projects that are assigned.Work with other Direct team members for decisions, and clarification as neededMust 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.pplications impacted by upgrades, Idele candidate should have previous experience implementing, and or upgrading. Other application experience can be considered.Vaya Raman7500 Fast PCRHIAC Particle CountersMaldi-tofVi-Cell Cell counterntaris IIWaters 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, Client Unicorn, Nova Biomedical Bio profile CDV and Flex2, Roche Cedex, Roche Light Cycler 480, FileMaker Pro, Bartender, Charles River Endoscan-V, Client 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 environmentFamiliarity with Automation systems such as SCADAs, PLCs, DCS, Client, HistoriansExperience with Computerized Systems Validation (CSV), 21 CFR Part 11 regulations, and Data Integrity complianceExperience 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 ControlVeeva - Document WorkflowsFamiliarity with Operational Excellence and/or Continuous Improvement processes
Knowledge and familiarity of following Tools and technologiesMS Office 365, MS Visio, MS ProjectCitrix, Windows Desktop, Windows Server, SQL Databases, LDAP,Group Policy, TCP/IP Networks, Server Virtualization, RDP, Backup and Restorerchitectures - 2 Tier, 3 Tier, On-premises, 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.
fterwards 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
Onsite Expectations:
For onboarding and training for the first few weeks should plan to be onsite 4-5 days a week. After onboarding and started working on projects, it is a minimum 3 days a week onsite, there will be times to be on site 4-5 days as needed.
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 solutionsHandle ad-hoc technical requests from both internal and external partners in accordance with projects that are assigned.Work with other Direct team members for decisions, and clarification as neededMust 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.pplications impacted by upgrades, Idele candidate should have previous experience implementing, and or upgrading. Other application experience can be considered.Vaya Raman7500 Fast PCRHIAC Particle CountersMaldi-tofVi-Cell Cell counterntaris IIWaters 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, Client Unicorn, Nova Biomedical Bio profile CDV and Flex2, Roche Cedex, Roche Light Cycler 480, FileMaker Pro, Bartender, Charles River Endoscan-V, Client 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 environmentFamiliarity with Automation systems such as SCADAs, PLCs, DCS, Client, HistoriansExperience with Computerized Systems Validation (CSV), 21 CFR Part 11 regulations, and Data Integrity complianceExperience 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 ControlVeeva - Document WorkflowsFamiliarity with Operational Excellence and/or Continuous Improvement processes
Knowledge and familiarity of following Tools and technologiesMS Office 365, MS Visio, MS ProjectCitrix, Windows Desktop, Windows Server, SQL Databases, LDAP,Group Policy, TCP/IP Networks, Server Virtualization, RDP, Backup and Restorerchitectures - 2 Tier, 3 Tier, On-premises, 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.
fterwards 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