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Computer analyst • boulder co

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QC Analyst

AgilentBoulder, CO, US
[job_card.full_time]

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AESBoulder, CO, United States
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QC Analyst

QC Analyst

AgilentBoulder, CO, US
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  • [job_card.full_time]
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Description

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).

Qualifications

  • 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

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least March 23, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $ - $ plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit

Travel Required:

Occasional

Shift:

Swing

Duration:

No End Date

Job Function:

Quality/Regulatory