QC Separation Analyst
at Life Science Recruitment
Cork, County Cork, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 13 Jul, 2024 | Not Specified | 14 Apr, 2024 | 2 year(s) or above | Capillary Electrophoresis,Pharmaceutical Industry | 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’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
EDUCATION & EXPERIENCE
- BSc (Honors) in a scientific/technical discipline.
- 2 years’ experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
- HPLC, Capillary Electrophoresis, UPLC/ Mass Spec experience
If interested in this posting please feel free to contact Sean McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.
Responsibilities:
- Achieves a high level of competency in laboratory methods and procedures to support in process and release testing of biotechnology products.
- Review and approval of laboratory test results.
- Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
- Executes validation, operation, maintenance, calibration and troubleshooting of equipment and it’s associated software.
- Write/executes reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
- Ensures that all testing is completed, reviewed and approved within agreed turnaround times.
- Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
- Trains other QC analysts in laboratory methods and procedures when required.
- Writes/updates and reviews TMs, SOPs and WIs as required.
- Writes and reviews invalid assays, non-conformances and deviations as required.
- Actively participates in JSI lean initiatives such as Kaizen, 6S and Gemba.
- Is an active member of the QC group and provide assistance with other group activities as required.
- Communicates relevant issues to the QC Team Leader promptly.
- Maintains and develops knowledge of analytical technology as well as cGMP standards.
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
BSc
Proficient
1
Cork, County Cork, Ireland