Lab Associate

3 days ago

Mumbai Maharashtra, India IQVIA Full time

Job Overview
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research.

Essential Functions
- 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.
- May perform secondary review of analytical results when signed-off as competent to do so for applicable instrument(s) and/or data type(s).
- Assists in the development and writing of new laboratory procedures and techniques.
- 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.

Qualifications
- High School Diploma or equivalent Req Or
- Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Req
- 6 months relevant lab experience Req Or
- Equivalent combination of education, training and experience Req
- Basic knowledge of lab principles.
- Basic knowledge of Good Laboratory Practices (GLP) and applicalbe 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.
- Applicable certifications and licenses as required by country, state, and/or other regulatory bodies.

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