Quality Control Scientist I

As a QC Scientist I, you will perform bench testing, including sample preparation, wet chemistry, standard weighing, and dilutions. Over time, you will receive training in HPLC and GC. You will support both the Oral Dose Solids and Nasals departments by conducting chemical and physical analyses to develop manufacturable multisource pharmaceutical products. You will also provide analytical support for the release of registration materials for regulatory submissions and assist in analytical method validation and transfer activities.

Responsibilities

• Conduct chemical and physical analyses to support product development and registration lot release.
• Provide analytical support for pre and post regulatory submission activities.
• Perform assigned analytical tasks within timelines, adhering to cGXP standards and company procedures.
• Follow work instructions, SOPs, and company practices for all tasks.
• Document analytical activities and results accurately and promptly, maintaining data integrity.
• Identify challenges in executing analytical methods and support troubleshooting activities.

• Proficiency in dilutions, sample preparation, biochemistry, and chemistry.
• Experience in quality control and chemical testing.
• Bachelor's degree in a Science field, preferably Chemistry or Biochemistry.
• Prior laboratory experience, including strong chemistry lab skills from academic or professional settings.
• Ability to work in a team environment and manage multiple tasks in a fast-paced setting.
• Excellent written and verbal communication skills.
• Capability to work under supervision using scientific judgment and professional competency.

• Bachelor's degree in Biology, Microbiology, Physics, Environmental Science, or Pharmaceutical Science with strong chemistry lab experience.
• Lab experience outside of academia is highly preferred.

This is a fast-paced environment where you will work in both the quality group and occasionally in the manufacturing area. The position requires working the 3rd shift, Monday to Friday, from 11 PM to 7:30 AM, with slight flexibility to work either 4-10 hour days or 5-8 hour days. The specific off day for 4-10 hour shifts will be determined after training to ensure daily coverage.

Pay and Benefits

The pay range for this position is $24.00 - $24.00/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 Columbus,OH.

Application Deadline

This position is anticipated to close on Jul 9, 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.