Lonza America Inc

Computer Systems Validation Specialist III

Lonza America Inc$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in computer science, engineering, or related field.
  • Over 3 years of experience in computer systems validation.
  • Hand-on experience in a cGMP facility for at least 3 years.
  • Familiarity with 21 CFR Part 11 and ISPE GAMP guidelines in connection to Computer Systems Validation.
  • Experience with analytical computerized systems.
  • Ability to work both independently and collaboratively.
  • Background in the biotech, pharma, or medical device industry.

Responsibilities

  • Lead assessments of new and changing computer systems for compliance.
  • Conduct risk assessments and review change requests.
  • Draft protocols and oversee GMP documentation revisions.
  • Act as QA CSV representative for various projects.
  • Author, review, and approve all validation lifecycle deliverables.
  • Schedule qualification activities to align with business objectives.
  • Revise SOPs for continuous improvement and compliance.

Benefits

  • Relocation assistance available for eligible candidates and families.
  • Opportunities for technical guidance and mentorship.
  • Involvement in key projects across different departments.
  • Exposure to customer audits and inspections as a CSV SME.
  • Continuous improvement opportunities through SOP revisions.
Full Job Description
Computer Systems Validation Specialist III

Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.

The Computer Systems Validation (CSV) Specialist III leads teams in assessing new and changing computer systems to ensure compliance with company policies and industry guidance. They conduct risk assessments, review change requests and test scripts, draft protocols, and oversee GMP documentation revisions. This role acts as the QA CSV representative for small and large-scale projects while providing technical guidance and mentorship to junior team members.

What you will do:

  • Perform all aspects of QMS process' - Change Control, Deviations,
  • CAPAs.
  • Perform Gap assessments to identify the gaps in processes and suggest remediation plans. Initiate the right Quality records (Deviations and CAPAs) to drive the remediation plan, as needed and execute all responsibilities as CSV project lead for projects.
  • Author/Review/Approve all end to end Computer system validation life-
  • cycle deliverables/activities.
  • Schedule qualification activities and personnel to meet business,
  • manufacturing, engineering and quality objectives.
  • Revise and maintain SOPs to ensure continuous improvement and
  • compliance to GROUP/CORP procedures.
  • Perform review of Engineering documents (P&IDs, SOPs, Specifications, Submittals, etc.).
  • Support Validation requests as a CSV SME, during Customer audits and inspections.


What we are looking for:

  • Bachelor's degree in computer science, engineering, or related field.
  • At least 3+ years of experience in computer systems validation.
  • 3+ years of Experience in working in a cGMP facility.
  • Experience with 21 CFR Part 11 and ISPE GAMP guidelines as they relate to Computer.
  • Systems Validation (especially for analytical computerized systems).
  • Works independently and in teams.
  • Background in biotech, pharma, or medical device industry.
  • Ability to work independently and on-site in Portsmouth NH.


Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits

Ready to shape the future of life sciences? Apply now.

About Lonza America Inc

Lonza America Inc is a subsidiary of Lonza Group, a Swiss multinational company that provides products and services to the pharmaceutical, biotech, and specialty ingredients markets. Lonza America Inc is responsible for the North American market and offers a range of products and services, including custom manufacturing, research and development, and quality control testing. The company has a strong focus on sustainability and has implemented various initiatives to reduce its environmental impact. Lonza America Inc was founded in 1897 and has since grown to become a leading provider of products and services in the pharmaceutical and biotech industries.
Learn more about Lonza America Inc
Size
16,218 employees
Industry
NASDAQ

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