QC Analyst

Agilent Technologies • Boulder, CO

1d • $27 - $42

About The Position

The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines. The Quality Control Analyst: Conducts routine and non-routine analysis of raw materials and in-process and finished formulations according to standard operating procedures Performs analyses, including biochemical and/or chemical analyses of products, analysis of raw materials, in-process items and finished products to ensure stability according toa established operating procedures Compiles data for documentation of test procedures that may include biochemical and chemical assays, stability program testing and formulation studies Calibrates and maintains lab equipment Participates in the preparation of investigations, summaries and reports May develop testing methods Reviews data obtained for compliance to specifications and reports abnormalities Revises and updates standard operating procedures as needed May perform special projects on analytical and instrument problem-solving This position will support Weekend Shifts, consisting of four, 10-hour shifts working Thursday thru Sunday 8 am to 6:30 pm (30 minute lunch break). Training will be Monday thru Friday for a minimum of six months on an 8-hour shifts (30 minute lunch break).

Requirements

• Bachelor’s or master’s Degree or equivalent experience in Analytical Chemistry or related life sciences field
• 1+ years' experience and/or training; or equivalent combination of education and experience
• Demonstrated knowledge of analytical equipment and instrumentation, HPLC experience working in a GMP environment is helpful

Responsibilities

• Conducts routine and non-routine analysis of raw materials and in-process and finished formulations according to standard operating procedures
• Performs analyses, including biochemical and/or chemical analyses of products, analysis of raw materials, in-process items and finished products to ensure stability according toa established operating procedures
• Compiles data for documentation of test procedures that may include biochemical and chemical assays, stability program testing and formulation studies
• Calibrates and maintains lab equipment
• Participates in the preparation of investigations, summaries and reports
• May develop testing methods
• Reviews data obtained for compliance to specifications and reports abnormalities
• Revises and updates standard operating procedures as needed
• May perform special projects on analytical and instrument problem-solving

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level