Skip to main content
Back to jobs

Computer Systems Validation Specialist

External
Lonza logoLonza · Us - Portsmouth, NH
Full-timeOn-site1w ago
ComplianceDocumentationLeadershipMentoringSCADA
Cover LetterConnect

Prepare for this interview

Elite

AI-generated questions, company research, and talking points tailored to this role


Responsibilities

  • Perform all aspects of QMS process' - Change Control, Deviations, CAPAs.
  • Execute all responsibilities as CSV project lead for simple projects.
  • Oversee/perform all CSV qualification activities for DeltaV and Syncade systems.
  • Perform Validation Maintenance of computerized systems.
  • Review/Revise CSV SOPs.
  • Perform review of Engineering documents (P&IDs, SOPs, Specifications, Submittals, etc..)
  • Assist with audits and inspections.

Requirements

  • Bachelor's degree in computer science, engineering, or related field.
  • 3+ years experience in Computer Systems Validation and in a cGMP facility.
  • 1+ years with Programmable Logic Controllers (PLC), Controls Automation, Process Control Systems, SCADA Systems, Distributed Controls Systems (DCS), Building Alarm Systems (BAS), Building Management Systems (BMS), Manufacturing Execution Systems (MES) required, DeltaV is preferred.
  • Experience leading projects and managing CAPAs and deviations.
  • Background in biotech, pharma, or medical device industry.
  • Strong attention to detail and ability to meet deadlines.
  • Ability to work independently and on-site in Portsmouth NH.
  • About Lonza:
  • Ready to shape the future of life sciences?

Benefits

Vision insurance

Additional Information

The Computer Systems Validation (CSV) Specialist Location : Portsmouth, NH. Relocation assistance is available for eligible candidates and their families. The Computer Systems Validation (CSV) Specialist helps to lead team members to assess new and changing computer systems to ensure compliance with company policies, procedures and industry guidance. The CSV Specialist will risk assess systems, review change requests and test scripts, draft protocols and initiate and review GMP documentation revisions. This position also provides guidance to junior team members and will be involved as the QA CSV representative during small and large-scale projects. What you will get: A collaborative and inclusive work environment. Opportunities for career growth and development. Access to cutting-edge technologies and tools. Competitive compensation and benefits package. Supportive leadership and mentoring. Commitment to ethical and sustainable practices. Access to our full list of global benefits: https://www.lonza.com/careers/benefits


Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Lonza? Share your experience

Interested in this role?

Apply on the company's website.

Cover LetterConnect