Dosimetry Lab Technician
at Abbott Laboratories
Kilkenny, County Kilkenny, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jul, 2024 | Not Specified | 04 May, 2024 | 2 year(s) or above | Electron Beam,Iso | 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:
EDUCATION & EXPERIENCE
- Third level Science / Manufacturing or equivalent qualification.
- Preferred two years’ work experience in a Manufacturing / Science / Quality or equivalent environment.
- Electron beam or other sterilisation technologies experience desirable.
- Knowledge in ISO 11137 desirable.
- Chemistry/Microbiology/Dosimetry Lab experience desirable.
Responsibilities:
- Perform a variety of sampling activities to support product manufacture in a cGMP regulatory environment.
- Perform dosimetric analysis, dose map execution and equipment maintenance, accordance with GLP, GMP and ISO 11137.
- Ensure that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs).
- Assist in the design and set-up of the site dosimetry lab program.
- Create and update documentation as needed.
- Support the set up and maintenance of laboratory equipment and consumables.
- Ensuring the laboratory is adequately stocked and resourced, with everything accurately labelled.
- Participate in validation activities as needed for dosimetry lab and equipment qualification program.
- Review and approval of laboratory test results.
- Complete records on time and review data for accuracy and completeness.
- Assist in the identification of root cause analysis and provide technical advice as needed.
- Support unplanned events and raise out of specification results in a timely manner and inform the Supervisor immediately of any such events.
- Initiate and complete CAPAs and change controls in accordance with site procedures.
- Trend data for environmental and product monitoring. This also involves the generation and presentation of quarterly and annual reports
- Maintain a “right first time” approach to quality records by ensuring accountability for functional responsibilities.
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Technician, Clinical Pharmacy
Graduate
Proficient
1
Kilkenny, County Kilkenny, Ireland