About the Role
As a Production Operator, you will manufacture, inspect, test, label, and package Class II/III medical device implant products within a Cleanroom environment adhering to stringent quality control systems under GMP standards.
Duties and Responsibilities:
* Perform duties assigned by the Production Supervisor or Designee.
* Carry out operations in cleanroom manufacturing areas according to documented procedures and practices.
* Complete and comply with documentation and procedures as required.
* Adhere to Good Manufacturing Practice requirements.
* Maintain high productivity and efficiency levels.
* Ensure safe working practices.
* Support new employee training.
* Participate in R&D activities for new products and devices.
* Promote cost-saving initiatives.
* Clear production lines according to guidelines.
* Operate computer applications as required.
* Perform other related tasks assigned.
Skills and Experience:
A leaving certificate qualification or equivalent education is required. Relevant experience in medical device manufacturing is desirable but not essential.
EEO/AA Disability/Veteran