Join a cutting-edge pharmaceutical team where your analytical expertise directly impacts the quality and safety of life-changing therapies. This is more than a lab jobits a chance to grow in a collaborative, innovation-driven environment with a company that values precision, integrity, and scientific excellence.
What Youll Be Doing- Execute routine and stability testing on pharmaceutical products using HPLC and other validated methods.
- Analyze samples for potency, purity, identity, and other critical quality attributes.
- Investigate and report non-conforming results and support resolution of analytical challenges.
- Perform instrument calibration and maintenance to ensure data integrity.
- Prepare reagents, maintain lab cleanliness, and uphold GMP/GLP compliance.
- Accurately document all findings in accordance with regulatory and internal standards.
- Bachelors degree or higher in Chemistry or a related physical science.
- 12 years of hands-on experience with HPLC and chromatographic techniques.
- Solid understanding of instrumental analysis, wet chemistry, and pharma quality systems.
- Strong attention to detail, documentation skills, and a proactive mindset.
- Ability to thrive in a fast-paced, regulated environment.
- Familiarity with SOPs, cGMPs, GLPs, and pharmaceutical regulatory frameworks.
- Excellent communication and time management skills.
- A passion for continuous learning and scientific problem-solving.
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 Cincinnati,OH. Application Deadline This position is anticipated to close on Jul 7, 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 ... for other accommodation options.