Quality Control Scientist I

QC Scientist I

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW!

Job Description

As a QC Scientist I, you will be engaged in bench testing, which involves tasks such as sample preparation, wet chemistry, standard weighing, and dilutions. Over time, you will receive training in High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). You will be trained in both the Oral Dose Solids and Nasals departments, conducting chemical and physical analyses to support the development of manufacturable multisource pharmaceutical products. Your role includes providing analytical support for the release of registration materials essential for regulatory submissions and assisting in analytical method validation and transfer activities.

Responsibilities

• Perform assigned analytical tasks in support of product development, registration lot release, and pre and post regulatory submission activities.
• Ensure activities are completed within assigned timelines and in compliance with cGXP's and company practices.
• Follow work instructions, SOPs, and company practices diligently.
• Accurately document analytical activities and results in a timely manner, maintaining data integrity.
• Adhere to written analytical procedures and identify execution challenges of analytical methods.
• Support troubleshooting activities as needed.

Essential Skills

• Proficiency in dilutions, sample preparation, biochemistry, quality control, and chemistry.
• Bachelor's degree in a science field (preferably Chemistry or Biochemistry, but Biology, Microbiology, or Pharmaceutical Science with strong chemistry lab experience is acceptable).
• Prior lab experience, which can be from academic settings or industry.
• Ability to work effectively in a team environment and manage multiple tasks in a fast-paced environment.
• Good written and verbal communication skills.
• Ability to work with supervision using scientific judgment and professional competency.

Additional Skills & Qualifications

• Experience in lab environments outside of academia is strongly preferred.

Work Environment

This role operates in a fast-paced environment, with responsibilities split between the quality group and occasionally the manufacturing area. The position is for the 2nd shift, Monday through Friday, from 2:00 PM to 10:30 PM, with some flexibility. Initially, the schedule is 5 days of 8-hour shifts, with the possibility of transitioning to a 4-day, 10-hour schedule after training. The company promotes from within, offering ample opportunities for growth and upward mobility.

Job Type & Location

This is a Contract to Hire position based out of Columbus, OH.

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 Nov 23, 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.