QC IT Application Analyst
Company: USDM Life Sciences
Location: Lexington
Posted on: November 19, 2024
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Job Description:
Job Title: QC IT Application Analyst Job Function: Quality
Consultant Location: Lexington, MA - Hybrid
Are you the right candidate for this opportunity Make sure to read
the full description below.
USDM Life Sciences is a premier consulting company with 20+ years
of experience assisting heavily regulated biotech, medical device,
and pharmaceutical companies with their GxP technologies to
accelerate growth. Our deep domain knowledge and technology
expertise in life sciences business processes are what sets us
apart. From strategy to implementation and adoption, we have
delivered thousands of GxP projects globally.
As part of the USDM team, you have the opportunity to work with
cutting edge technologies through our many partnerships with
companies like Microsoft, Google, Oracle, DocuSign, Box, and many
more. From molecule to market, you will help connect technology,
people, and data in new ways to generate real-time insights to
improve business outcomes for USDM's clients. Are you ready to make
an impact and drive real digital transformation in life
sciences?
Founded in Santa Barbara in 1999, USDM has grown to a progressive,
global company with 300+ remote employees and offices throughout
the US, Canada, and Germany.
Nature and Scope of Job
USDM Life Sciences is seeking an experienced QC IT Application
Analyst who will collaborate with the business and IT teams to
provide project support for Quality, Validation and Product
Development.
Primary Responsibilities
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.
Additional Responsibilities
Other duties as assigned.
Qualifications
IT Experience deploying and supporting Quality and Manufacturing
Systems including Analytical Instruments.
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
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.
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).
Education & Certifications
Bachelor's degree or equivalent in information technology, computer
science, engineering, or business administration.
Working Conditions
The working conditions described here are representative of those
that must be met by an employee to successfully perform the
essential responsibilities and functions of the job and are not
meant to be all inclusive. Reasonable accommodation may be made to
enable individuals with disabilities to perform the essential
responsibilities and functions of the job.
Unless reasonable accommodations can be made, while performing this
job the staff member shall:
Prolonged periods of sitting or standing at a desk and working on a
computer in an environmentally controlled home office
environment.
Operate other office productivity machinery, such as a calculator,
scanner, or printer.
Frequently communicate with stakeholders via telephone, email, or
instant message. Must be able to exchange accurate information in
these situations.
Travel to client site for onsite work as needed.
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.
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 osite 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.
Equal Opportunity Statement
USDM Life Sciences is an equal opportunity employer. All qualified
applicants will receive consideration for employment without regard
to race, color, religion, sex, sexual orientation, gender identity,
national origin, disability, or status as a protected veteran.
Disclaimer
This job description is intended to describe the general nature and
the level of the work being performed by the people assigned to
this position. It is not intended to include every job duty and
responsibility specific to the position. USDM Life Sciences
reserves the right to amend and change responsibilities to meet
business and organizational needs as necessary.
Keywords: USDM Life Sciences, Covington , QC IT Application Analyst, Professions , Lexington, Kentucky
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