• Urgently Hiring: Pharmaceutical QC Scientist I

    Actalent (Columbus, OH)


    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

    Join a dynamic team as a QC Scientist I where you will engage in bench testing, including sample preparation, wet chemistry, standard weighing, and dilutions. Over time, you will be trained on advanced techniques such as HPLC and GC in both the Oral Dose Solids and Nasals departments. You will conduct chemical and physical analyses to support the development of manufacturable multisource pharmaceutical products and provide analytical support for the release of registration materials in support of regulatory submissions. Your role will also include assisting in analytical method validation and transfer activities.

    Responsibilities

    + Perform assigned analytical tasks to support product development, registration lot release, and pre- and post-regulatory submission activities.

    + Conduct tasks within assigned timelines and ensure compliance with cGXP's and company practices.

    + Follow work instructions, SOPs, and company practices to maintain data integrity.

    + Document analytical activities and results accurately and in a timely manner.

    + Identify execution challenges of analytical methods and support troubleshooting activities.

    Essential Skills

    + Proficiency in dilutions, sample preparation, biochemistry, and chemistry.

    + Experience in quality control and chemical testing.

    + Bachelor's degree in a science field; preferred in Chemistry or Biochemistry.

    + Prior laboratory experience, preferably outside of academia.

    + Ability to work in a team environment and manage multiple tasks in a fast-paced setting.

    + Strong written and verbal communication skills.

     

    Additional Skills & Qualifications

     

    + Candidates with a Bachelor's degree in Biology, Microbiology, or Pharmaceutical Science with strong chemistry lab experience are considered.

    + Ability to work with supervision using scientific judgment and professional competency.

    Work Environment

    This is a fast-paced environment where you will work primarily within the quality group and occasionally in the manufacturing area. The position operates on a 2nd shift schedule from Monday to Friday, 3 PM to 11:30 PM, with some flexibility. Initially, you will work five 8-hour shifts, with the potential to transition to a four 10-hour shift schedule after training.

     

    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 Jan 12, 2026.

    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 [email protected] (%[email protected]) for other accommodation options.