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Hours Full-time, Part-time
Location Ontario, CA
Ontario, California

About this job

ROLE AND RESPONSIBILITIES
* Read and understand Standard Operating Procedures (SOP) related to job function.
* Analyzes and maintains data per applicable SOPs.
* Documents activities in a cGMP manner.
* Recognize problems and inform the lab manager to perform corrective actions.
* Performs investigation and resolution of out-of-spec events.
* Performs raw material testing.
* Prepares reagents and solutions as necessary to conduct analyses.
* Understand the operation and maintenance of laboratory equipment.
* Maintain instrumentation logbooks/logs for laboratory equipment.
* Adhere to laboratory safety rules.
* Other duties as assigned.

JOB DESCRIPTION:
* Perform QC Documentation of all finished products before going out for sale.
* Follow standard SOPs and batch records within a cGMP system.
* Analyze and maintain data and prepare data reports.
* Perform investigation and resolution of out-of-specification events.
* Prepare reagents and solutions as necessary to conduct analyses.
* Perform routine maintenance of laboratory equipment.
* Work independently and / or as part of a team.
* Possess good oral and written communication skills and be capable of following a chain of command.
* Computer skills - Microsoft Windows and Excel, Word, PowerPoint

* Familiarity with Lab procedures and chemical compositions to speak with customers about products.

* Interact and address all customer complaints.

Qualifications:

  • Bachelor's degree (BS) in Chemistry with 1-3 or more years experience in an analytical lab or a Master's degree (MS) in Analytical Chemistry or related field with 1 or more years experience.
  • 1-3 years of Hands-on experience on wet chemistry and document control. QA/QC Doc control would be ideal
  • Keep organized records and provide technical reports as needed.
  • Solid working knowledge of MS Office programs.
  • A good team player.
  • Possess proficient use of the English Language both written and verbal.

Preferred Qualifications:

  • Pharmaceutical background preferred Nutraceutical acceptable
  • Capable of writing protocols and reports
  • Experience in an FDA regulated environment a plus.




About Aerotek:

Our people are everything. As a Best of Staffing® Client and Talent leader, Aerotek® Inc. has distinguished itself as a leader in recruiting and staffing services, by having a deep understanding of the intersection of talent and business. As a strategic partner to more than 17,000 clients and 300,000 contract employees every year, Aerotek's people-focused approach yields competitive advantages for its clients and rewarding careers for its contract employees. Headquartered in Hanover, Md., Aerotek operates a network of over 230 non-franchised offices with more than 6,000 internal employees dedicated to serving our customers. Aerotek is an operating company of Allegis Group, a global talent solutions provider. To learn more, visit .

Aerotek is acting as an Employment Agency in relation to this vacancy.