QC Scientist I

Hours: 2nd shift

As a QC Scientist I, you will engage in bench testing activities including sample preparation, wet chemistry, standard weighing, and dilutions. Over time, you will be trained in advanced techniques such as HPLC and GC. Your role will involve conducting chemical and physical analyses to support the development of pharmaceutical products, providing analytical support for regulatory submissions, and assisting with method validation and transfer activities.

Responsibilities

• Conduct chemical and physical analyses to support the development of manufacturable pharmaceutical products.
• Provide analytical support for the release of registration materials in support of regulatory submissions.
• Assist with analytical method validation and transfer activities.
• Perform assigned analytical tasks within designated timelines and in compliance with cGXP's and company practices.
• Follow work instructions, SOPs, and company practices, documenting analytical activities and results accurately and in a timely manner.
• Maintain the integrity of data, ensuring right-first-time documentation.
• Identify execution challenges of analytical methods and support troubleshooting activities.

• Proficiency in dilutions and sample preparation.
• Solid understanding of biochemistry and quality control.
• Bachelor's degree in a science field, preferably Chemistry or Biochemistry.
• Prior lab experience, which may be obtained from academic settings.
• Good written and verbal communication skills.
• Ability to work in a team environment and manage multiple tasks in a fast-paced setting.

• Candidates with degrees in Biology, Microbiology, or Pharmaceutical Science are considered, provided they have strong chemistry lab experience.
• Lab experience outside of academia is strongly preferred.
• Ability to work under supervision using scientific judgment and professional competency.

The position is based in a fast-paced environment, involving work in both quality control and occasionally in the manufacturing area. The shift is scheduled for 2nd shift, Monday to Friday, from 2 PM to 10:30 PM with some flexibility. After training, the schedule may transition from five 8-hour shifts to four 10-hour shifts.

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 Jun 26, 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.