Description Candidate will be responsible for technical writing and execution of existing validation and optimization efforts in the QC lab. Technical writing will include report writing, documenting test methods, protocols and specifications. Chemists will perform and document validation methods for HPLC instrumentation per Client SOPs, documenting per GDPs, and meeting all requirements of Client’s QMS. Focus is expected to be on HPLC, but Client can provide training on additional techniques like GC, KF and ICPMS where needed. Specific Tasks: • Prepare technical reports, test methods, protocols and specifications consistent with client's QMS requirements • Sample preparation and execution of existing validation methods for existing compounds o HPLC analysis • Optimize existing methods where possible • Capture and document all test method data in accordance with cGMPs Skills Hplc, Technical writing, Gmp Additional Skills & Qualifications This role will focus on technical writing for the initial six months, then shift to more of a hybrid lab and technical writing role. • 2+ years of experience for required capabilities • BS in Chemistry or similar • Experience running sample analysis via HPLC instrumentation • Experience documented via good documentation practices • Comfortable working with respirator, including PAPR Experience Level Intermediate Level Pay and Benefits The pay range for this position is $28.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job 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) Workplace Type This is a fully onsite position in Madison,WI. Application Deadline This position is anticipated to close on Aug 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.