• Sr. Associate Scientist - Plate Based

    Actalent (Sanford, NC)


    Job Title: Scientist - Plate BasedJob Description

     

    The Scientist will support the Quality Control Method Transfer and Validation team by performing method validation activities, including drafting protocols and reports, executing validation assays, and conducting data analysis. The Scientist will also be responsible for reviewing reports and data in accordance with cGMP and data integrity principles.

    Responsibilities

    + Independently conceptualize, plan, and execute laboratory experiments.

    + Collaborate with colleagues and subject matter experts to determine the most suitable analytical methodologies to support project initiatives.

    + Lead and manage multiple projects, assisting teams in developing effective strategies for analytical needs and controls.

    + Engage with the method development team and participate in both in-process and final product sample analyses.

    + Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes.

    + Prepare technical reports, critically review data, and evaluate new instrumentation and analytical techniques/approaches as required.

    + Independently analyze experimental data and provide conclusive insights.

    + Mentor junior scientists and offer technical guidance when required.

    + Support the technical leads and the Sr. Scientist with project activities to meet deadlines.

    Essential Skills

    + 4-6 years of industry experience in pharmaceutical chemistry.

    + Proficiency in GMP, PCR, and ELISA.

    + Ability to independently execute laboratory assays, draft protocol deviations under supervision, and perform data reviews.

    + Experience with Spectramax and Lowry.

    Additional Skills & Qualifications

    + Bachelor's, Master's, or PhD in a relevant field with applicable experience.

    + Assay development, method validation, and method transfer experience.

    + Knowledge of cGMP, quality control, LIMS, and immunoassays.

    Work Environment

    This role is within a large pharmaceutical manufacturing organization focused on vaccine and mAb intermediate manufacturing. The work environment includes both office and lab settings. The position operates on a 1st Shift schedule from Monday to Friday, 8 AM to 5 PM, with occasional weekend work required on a rotating basis for specific projects.

     

    Job Type & Location

     

    This is a Contract position based out of Sanford, North Carolina.

    Pay and Benefits

    The pay range for this position is $30.00 - $40.00/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 Sanford,NC.

     

    Application Deadline

     

    This position is anticipated to close on Oct 20, 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 [email protected] (%[email protected]) for other accommodation options.