Production Technician
at Johnson Johnson
Limerick, County Limerick, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jul, 2024 | Not Specified | 05 May, 2024 | 2 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
WE WOULD LOVE TO HEAR FROM YOU IF YOU HAVE THE FOLLOWING ESSENTIAL REQUIREMENTS:
- A Leaving certificate or equivalent
- Minimum 2 years’ experience in a similar role
- Previous relevant experience in a production environment
- Ability to work on own initiative
- Attention to detail and flexible work ethic
· Experience working in the medical device environment (Pneumatic systems, PLCs, Machine Automation, Equipment Set up, Pick and Place Machinery)
- Training and experience in Packaging/print equipment, High volume manufacturing, Mechanical setup, Injection moulding, Electromechanical)
NOTE:
Responsibilities and accountabilities will vary for all positions and the scope of individual roles may not be limited to the contents of this position description. QUMAS procedures will define responsibilities from time to time and each manager is responsible for complying with these processes, which supplant any responsibility outlined within. As such, adherence to company procedures is also a responsibility of any roles encompassed within this Job Description
Responsibilities:
THE RESPONSIBILITIES & THE IMPACT YOU WILL HAVE:
The role is to be responsible for supporting manufacturing processes by implementing all aspects of process improvement, equipment setup, testing, documentation, problem correction and related tooling.
- Updates supervisor of work status or problems with recommendations for improvement or correction
- Assists in modifying procedures to improve equipment operation or processes
- Responds to basic system alarms and reset alarms as necessary
- Records assignments and prepares documentation concerning materials, parts used, concepts, designs, drawings, and processes
- Conducts testing protocols and documents results
- Implements manufacturing phase-in of new products or product changes
- Identifies safety issues and provide support in their resolution
Participates specialized studies or experiments as needed
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Other Industry
Pharma / Biotech / Healthcare / Medical / R&D
Other
Trade Certificate
A leaving certificate or equivalent
Proficient
1
Limerick, County Limerick, Ireland