About the Role
:
As a Production Operator you will be responsible for the manufacture, product-inspection, testing, labelling & packaging of Class II / III medical device implant products within a Clean room environment. All operations are conducted under stringent quality control systems to GMP standards. The successful candidate will work as part of a team to maintain high quality/performance/delivery standards on all Aran Biomedical products.
Duties and Responsibilities:
1. Perform all duties assigned by the Production Supervisor or Designee.
2. Carry out operations to documented procedures and practices in the cleanroom manufacturing areas, including processing, packing, and labelling.
3. Complete and comply with all documentation/procedures as required
4. Adhere to all Good Manufacturing Practice requirements
5. Strive to meet Production Output, Yield, Efficiency and Productivity Targets
6. Ensure that all duties are carried out in a safe manner.
7. Support the training of new employees.
8. Support R&D activities of new products and devices as required
9. Assist in and become involved in cost saving ideas, projects and initiatives.
10. Perform line clearances to strict guidelines.
11. Perform computer applications as required.
12. Performs other related duties, as assigned
Skills and Experience:
Successful candidate must have a leaving certificate qualification or equivalent level of education is required. Relevant experience in a medical device-manufacturing environment is desirable, but not essential.
U.S. Applicants: EOE/AA Disability/Veteran