
QC Technical Writer
- Madison, WI
- $28.00-30.00 per hour
- Contract
- Full-time
- Prepare technical reports, test methods, protocols, and specifications consistent with the client's QMS requirements.
- Conduct sample preparation and execute validation methods for existing compounds, specifically focusing on HPLC analysis.
- Optimize existing methods where possible.
- Capture and document all test method data in accordance with cGMPs.
- Proficiency in HPLC with actual, recent hands-on use, not just theoretical knowledge.
- Technical writing skills, especially for laboratory validation documentation, including writing technical reports, test methods, protocols, and specifications.
- Experience working within the life sciences industry, specifically within a cGMP/FDA regulated facility (non-biologics).
- 2+ years of experience in relevant capabilities.
- Bachelor's degree in Chemistry or a similar field.
- Experience running sample analysis via HPLC instrumentation.
- Experience with good documentation practices.
- Comfortable working with a respirator, including PAPR.
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)