IQA Technician
at Abbott Laboratories
Cavan, County Cavan, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Food Science,Facebook,Linkedin | 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:
ABOUT ABBOTT
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 113,000 colleagues serve people in more than 160 countries.
Abbott serves the Irish market with a diverse range of healthcare products including diagnostics, medical devices and nutritionals products. In Ireland, Abbott employs o6,000 people across ten sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations and shared services in Dublin and Galway. We have been operating in Ireland since 1946.
EDUCATION & EXPERIENCE
- Diploma in Food Science or equivalent or cert with relevant manufacturing experience.
- Minimum of 12months experience in a regulated environment would be an advantage
Connect with us at www.abbott.com or https://www.ie.abbott/, on LinkedIn at www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews
Responsibilities:
- Responsible for sampling, checking and subsequently releasing or rejecting commodities coming to site.
- Responsible for ensuring all commodities on site have full traceability both visually and virtually.
- Support the packing lines with can tear downs daily and support them with queries regarding materials being used on the line.
- Ensuring IQA area is always audit ready by following site GMP and GLP.
- Overseeing the sites batch files, recording, and filing into the Kardex.Support ingredient and packaging trials on site.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Technician
Diploma
Proficient
1
Cavan, County Cavan, Ireland