Title : Associate Quality Control
Location : Thousand Oaks, CA
Contract position
Ideal Candidate :
- Candidates must have an educational background in Chemistry or Biology, along with experience in GMP within the biotech or pharmaceutical industry, with a focus on pipetting techniques.
- A minimum of 2 years of GMP experience is preferred.
- Proficiency in software tools such as Teams, Excel, and Word is essential.
- Familiarity with SharePoint, SmartSheets, or LIMS is a plus.
- Strong communication skills are also a key requirement for this role.
Job Details :
Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities : - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - 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 logbooks.
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