At Smith+Nephew we design and manufacture technology that takes the limits off living
Job Summary
At Smith+Nephew we design and manufacture technology that takes the limits off living.
This role will require the incumbent to lead investigator for authoring change control documentation, authoring / supporting deviations / manufacturing non-conformances and CAPAs, and authoring risk assessments.
Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability.
Matching Summary
At Smith+Nephew we design and manufacture technology that takes the limits off living.
Skills & Requirements
Must-have
PLC, HMI, and SCADA systems
URS development and FAT execution
GMP and Part 11 standards
Risk assessments and gap assessments
Automation Subject Matter Expert (SME)
Nice-to-have
Mentoring junior team members
Influencing team members and managers
Optimizing existing automation processes
Key Requirements
Bachelor's degree in engineering
Minimum 3 years of experience in Pharmaceutical/Biotech