QC Informatics Specialist

Pharmaron

$80K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • MSc or BSc in Chemistry, Computer Science, or related fields with 5+ years of GxP experience.
  • Proven experience in an IT support role with a foundational understanding of data structures.
  • Direct experience with laboratory informatics systems, specifically LIMS.
  • In-depth knowledge of GxP topics including QMS, ALCOA+, and 21 CFR Part 11.
  • Strong communication skills and the ability to present complex information effectively.

Responsibilities

  • Lead improvements in laboratory information handling and software workflows.
  • Manage GxP software upgrades and installations to ensure operational continuity.
  • Conduct GxP qualification activities as part of the CSV lifecycle.
  • Demonstrate expertise in complex software platforms within laboratory settings.
  • Train end users and provide ongoing system support.
  • Act as a liaison between end users and IT to prioritize resources.
  • Support audits and compliance reviews for the department.

Benefits

  • Comprehensive Medical, Dental & Vision Insurance with employer contributions.
  • 401(k) Retirement Plan with generous employer matching.
  • Generous Paid Time Off, Sick Leave & Company Holidays.
  • Employer-funded Health Savings Account contributions, plus flexible spending accounts.
  • 100% Employer-paid Life Insurance, AD&D, and Disability Insurance programs.
  • Access to Employee Assistance Program and wellness resources.
  • Family-friendly benefits including fertility support and maternity resources.
  • Opportunities for professional development and career growth.
Full Job Description
Position: Computer System Validation/QC Informatics Specialist

Salary Range: $80,000 - $120,000/yr.

Location: Coventry, RI (On-site)

What You'll Do

To support process chemistry and manufacturing activities through management of laboratory data software platforms and workflows. This role is positioned within the Quality Control & Analytical department to develop and support their requirements and workflows and to act as liaison with IT and QA to minimize downtime, improve effectiveness and maintain compliance related to laboratory data generation, storage, and use.

Key Responsibilities
  • With the support of the reporting manager in the Quality Control & Analytical department, lead laboratory improvement efforts related to laboratory information handling such as custom report generation, ELN, LIMS system configuration, data storage/organization, and pharmaceutical data workflows.
  • Liaising with appropriate technical and IT stakeholders to manage GxP software upgrades, installations, and roll outs to ensure business continuity and effectiveness are maintained and improved.
  • Author, review, and perform GxP qualification activities related to QCA as part of the Computer System Validation (CSV) life cycle e.g. GxP Risk & Impact Assessments, URS/FS, Qualification Plan, IQ, OQ, PQ, Requirement Tractability Matrix, Quality Summary Report, periodic reviews and decommissioning activities.
  • Demonstrating expertise in site-wide, complex software platforms e.g. NuGensis LMS, SDMS, ELN, Empower 3 etc. as well as various other standalone laboratory system software used within QCA and Process Chemistry.
  • Support System Owners within business functions with training end users in the use of the system.
  • Liaise between end users and IT to clearly communicate business priorities and ensure that appropriate resources are used to maintain ongoing business operations.
  • Build effective business relationships with all stakeholders.
  • Support departmental or site audits as directed by manager/supervisor as necessary

What We're Looking For
  • MSc or BSc in Chemistry, or Computer Science, or related fields with minimum of 5 years of GxP experience.
  • If qualified in chemistry or a related field, then strong experience in an IT supporting role must be demonstrated including a basic understanding of data structures, programming, and/or information systems.

If qualified in computer science or a related field, then strong experience in an analytical laboratory supporting role must be demonstrated including a basic understanding of common chemistry terminology, application, and laboratory workflows.
  • Direct experience with laboratory informatics (LIMS) systems.
  • Understanding of common GxP topics including QMS, ALCOA+, 21 CFR Part 11, and Data Integrity principles.
  • Evidence of ability to effectively work cross-functionally between IT and scientific teams
  • Working knowledge of applicable FDA, EMA, GAMP, and/or ICH guidance as it relates to data integrity.
  • Evidence of ability to manage stepwise implementation and qualification projects.
  • Good knowledge on pharmaceutical compliance and latest industry requirements.
  • Functional experience in the technical administration of complex laboratory informatics software platforms such as NuGenesis LMS, SDMS and ELN.
  • Effective written and oral communication skills, including the ability to effectively present complex information to colleagues.
  • Effective in managing multiple competing activities and delivering to timelines.
  • Ability to work professionally in a cross-functional environment and clearly reinterpret/translate concepts across IT and Laboratory staff.

Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

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