QC Scientist I

Indotronix was founded in April, 1986 in Poughkeepsie, NY. Today, Indotronix is headquartered in Rochester, NY and is part of the Indotronix Avani Group.The genesis of Indotronix’ initial success was as an IT Consulting Services Supplier to IBM. Since then we have continued to add Fortune 500 clients and awards to our roster and delivered staffing services valued at over $1 billion across industry verticals. Today we are recognized as an invaluable Supplier of IT, Engineering, Clinical, Scientific, Professional resources by our clients., several of whom have retained Indotronix for an average of 10+ years.

Job Title: QC Scientist I
Location: Fremont, CA 94538
Duration: 6 Months
Pay Rate: $30/hr on W2

Position Summary

Using standard operating procedures (SOP) and good manufacturing practices (GMP), the Engineer/Scientist I will perform testing of intermediate and raw materials. The Engineer/Scientist I will be responsible for all aspects of laboratory testing, such as sample receipt, data generation, product verification, data analysis and summarization, instrument operation, and other QC lab supporting activities.

Responsibilities:

• Conducts analytical and functional testing of raw materials and intermediates according to approved SOPs as part of QC Raw Material testing.
• Perform testing using chemistry clinical analyzers and document test results accurately using Excel spreadsheets and workbooks.
• Documents test results, complete batch records, document problems and other relevant information under cGMPs.
• Perform simple revisions and updates to QCs SOPs and/or worksheets as necessary, and initiate procedure change orders.
• Summarize test data, maintain lot histories and evaluate data for trends and discrepancies.
• Performs other responsibilities to support the needs of the department as assigned by Supervisor.

Minimum Requirements/Qualifications:

• Minimum BS/BA in Chemistry, Biochemistry, or Bioscience with 0-2 yrs Quality Assurance/Quality Control experience, preferably in the medical diagnostics industry.
• Strong laboratory skills including pipetting, safety, and hazardous chemical handling.
• Understanding of cGMP and how it applies to the work environment is preferred.
• High level of reading comprehension skills.
• Ability to follow written and verbal directions with a high level of accuracy.
• Must be able to write clear, understandable documentation.
• High level of verbal communication skills.
• Intermediate word processing and spreadsheet software skills.
• Ability to manage multiple tasks simultaneously.
• Ability to work independently.
• Ability to perform simple data analysis and to summarize results.
• Basic math skills including calculation of concentrations and dilutions and a strong grasp of algebraic concepts

All your information will be kept confidential according to EEO guidelines.