Generate Validation Protocols and reports within the Engineering department.
Generate protocols and reports.
Analysis of Validation Data.
Revise redline documentation.
Assist in the investigation and completion of Capa’s and Non conformances related to the engineering group.
Communicate with customers in relation to documentation follow-up.
Assist in establishing of documentation for the introduction of new and revised projects.
Contribute to Engineering improvement, cost improvement and other projects in accordance with Company policies and goals.
Perform other related duties as assigned.
Preferred degree or equivalent in Engineering or Quality.
Familiarity with Medical Device and Pharmaceutical Products and Industries.
Knowledge of Documentation Systems and Microsoft Office package.
Ability to cope with pressure and tight deadlines.
Self-motivated and work without supervision.
Two years’ experience in Medical Device/Healthcare industry.Apply for this job.