Lab Associate (routine bench)
at Q Solutions
Singapore, Southeast, Singapore -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 21 Nov, 2024 | Not Specified | 23 Aug, 2024 | N/A | Instrumentation,Terminology,Computer Skills,Laboratory Equipment,Data Science,Technology Solutions,Chemical Handling,Clinical Practices,Laboratory Safety | 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:
QUALIFICATIONS
- Bachelor’s Degree in healthcare-related fields.
- Prior / Current relevant laboratory experience.
- Basic knowledge of lab principles, coupled with Good Laboratory Practices (GLP) / Good Clinical Practices (GCP) and applicable regulatory agency standards.
- Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.
- Knowledge of laboratory equipment, instrumentation and terminology used in the area of responsibility.
- Basic computer skills.
- Ability to maintain effective reporting procedures and control workflow.
- Ability to effectively collaborate with internal stakeholders.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.co
Responsibilities:
- Performs routine analysis of specimens and documents results in accordance with SOPs and applicable regulatory guidelines.
- Evaluates validity of analytical results against the algorithms displayed by the lab computer system.
- Identifies and documents potential performance errors or otherwise unusual results and escalate to senior lab personnel.
- Responsible for preparation of buffers and solutions for analysis, as required.
- May perform secondary review of analytical results when signed-off as competent to do so for applicable instrument(s) and/or data type(s).
- Responsible for post analysis sample and reagent storage.
- Assists in the development and writing of new laboratory procedures and techniques.
- Assists in good housekeeping of the lab environment, consistent with 6S standards.
- Notifies appropriate staff of supply shortages.
- Responsible for clear, accurate, and timely communications with cross functional stakeholders.
- Participates in continuing education through self-study, attending in-services and lectures and meetings.
- Supports safety, quality, and 6S requirements and initiatives.
- Complies with company’s procedures and applicable regulatory requirements.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Healthcare-related fields
Proficient
1
Singapore, Singapore