Computer Systems Validation Engineer
Location: Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
The Computer Systems Validation (CSV) Engineer will, as an individual contributor, identify and implement industry best practices through an extensive industry network and detailed knowledge of applicable regulations. During the scoping portion of these improvement projects the person in this role will work with other experienced members of the CSV team to identify roadblocks and additional efficiencies. Additional day to day tasks will include risk assessing systems, reviewing change requests and test scripts, drafting protocols and initiating and reviewing GMP documentation revisions.
What you will get:
Competitive salary and comprehensive benefits package.
Opportunities for career development and advancement.
Supportive and collaborative team environment.
Access to cutting-edge technology and tools.
Commitment to employee well-being and safety.
Inclusive workplace culture.
Recognition and reward for your contributions.
Access to our full list of global benefits: https://www.lonza.com/careers/benefits
What you will do:
Lead efforts between internal customers and CSV to ensure assigned activities are prioritized, communicated in an effective and timely manner, and completed on time.
Accountable for maintaining full knowledge of Lonza's policies/procedures, 21 CFR Part 11, Data Integrity, ICH Q7A requirements and GAMP and the underlying principles of each.
Perform all aspects of Quality Systems Management (QSM) processes (Change Control, Deviation, Corrective and Preventable Actions) as well as Validation Maintenance of computerized systems.
Participate in audits and inspections as a Subject Matter Expert.
Own, revise and maintain computer systems validation SOPs (Standard Operations Procedures).
Function as CSV SME in Inspections and Audits.
Mentor and train junior members of the department.
What we are looking for:
Bachelor’s degree required, preferred in computer science, engineering, or other sciences.
Minimum of 5 years of experience working with automation and/or computerized system validations.
Minimum 2 years’ experience with Controls Automation, Process Control Systems, Distributed Systems, Manufacturing Execution Systems (MES) required, DeltaV preferred.
Prior experience leading or managing projects beneficial.
CAPAs and deviations experience desired.
Biotech/Pharma/Medical Device/Medical or biologics industry experience required.
Ability to work independently and meet deadlines successfully.
Ready to shape the future of life sciences? Apply now.
