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Quality Control Associate
Randstad Life Sciences US • West Greenwich, RI 02817 • Posted 1 day ago via LinkedIn
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In-person • Full-time • $33.50/hr • Contract • Entry Level
Job Highlights
Using AI ⚡ to summarize the original job post
The Quality Control Associate role involves performing routine procedures to support testing within Quality Control, including sample collection, handling, and testing equipment/laboratory support. This position is responsible for documenting, computing, compiling, interpreting, and entering data into computerized systems, maintaining and operating specialized equipment, and initiating and/or implementing changes in controlled documents. The role requires compliance with safety guidelines and cGMPs/CFRs.
Responsibilities
- Performing routine laboratory procedures
- Documenting, computing, compiling, interpreting, and entering data into computerized systems
- Maintaining and operating specialized equipment
- Initiating and/or implementing changes in controlled documents
- Complying with safety guidelines and cGMPs/CFRs
Qualifications
Required
- Some lab experience
- Ability to comply with safety guidelines and cGMPs/CFRs
Preferred
- GMP laboratory experience
Full Job Description
Associate Quality Control
Contract: 1 year
Location: West Greenwich, RI
Pay Rate: $33.5/hr
Job Details:
- Under general supervision, this position will perform routine procedures to support testing within Quality Control.
- Tasks may include but not limited to performing sample collection, sample handling, testing equipment/laboratory support.
This position will be responsible for one or more of the following activities:
- Performing routine laboratory procedures
- Documenting, computing, compiling, interpreting, and entering data into computerized systems
- Maintaining and operating specialized equipment
- Initiating and /or implementing changes in controlled documents.
- Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory notebooks.
Skills:
- Some lab experience is preferred. no academic research experience, would like a GMP lap exp.
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