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Quality Control Chemist Jobs

Company

MillenniumSoft Inc
Address San Jose, CA, United States
Employment type CONTRACTOR
Salary
Category IT Services and IT Consulting
Expires 2023-08-05
Posted at 10 months ago
Job Description
Position : Quality Control Chemist


Location : San Diego, CA


Duration : 6 Months


Total Hours/week : 40.00


Client: Medical Device Company


Job Category: Quality


Level Of Experience: Mid-Level


Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)



  • Identifies non-compliance within regulations and standards
  • Follow standard practices and procedures in analyzing situations or data from which answers can be readily obtained.
  • Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements and raises concerns/issues to the management.
  • Quality control chemists prepare and test samples from all phases of a manufacturing or other handling process, with the goal of determining if the substance meets the standards or requirements of the project. Responsible for conducting routine and non-routine analysis of raw materials, in-process and finished goods under limited supervision according to Standard Operating Procedures.
  • Coordinates equipment maintenance program in QC including calibration and preventative maintenance. Contacts vendor for service when needed.
  • Works on problems of diverse scope where analysis of situations or data requires evaluation of identifiable factors.
  • Conducts tests on raw materials, in process and finished goods as assigned.
  • Promotes a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices
  • Participate and support legacy and new product validation activities.
  • Is proficient at operating instrumentation, including cytometers.


Education And Experience


  • A minimum of 1year experience in a FDA or ISO/GMP regulated production environment
  • Requires a minimum of a bachelor’s degree in biological sciences or related field and a minimum of 1 years of hands on laboratory experience in a reagent process development or reagent manufacturing environment.


Assets


  • Familiarity with basic flowcytometry technology
  • Effective written and communication skills