<p>Job Title: Scientist - Plate Based</p> <p>Job Description</p> <p>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 role also involves procedural updates, reviewing reports, and ensuring data integrity in accordance with cGMP principles.</p> <p>Responsibilities</p> <ul> <li>Independently conceptualize, plan, and execute laboratory experiments. </li><li>Collaborate with colleagues and subject matter experts to determine suitable analytical methodologies for project initiatives, utilizing computational predictive tools, modeling software, and data visualization tools as necessary. </li><li>Lead and manage multiple projects, assisting teams in developing effective strategies for analytical needs and controls. </li><li>Engage with the method development team and participate in in-process and final product sample analyses. </li><li>Author relevant sections of technical reports to support interdepartmental technology and method validation and transfer processes. </li><li>Prepare technical reports, critically review data, and evaluate new instrumentation and analytical techniques/approaches as required. </li><li>Independently analyze experimental data and provide conclusive insights. </li><li>Mentor junior scientists and offer technical guidance when required. </li><li>Support the technical leads and the Sr. Scientist with project activities to meet deadlines. </li></ul> <p>Essential Skills</p> <ul> <li>Experience in cGMP practices. </li><li>Proficiency with Anthrone, Spectramax, and ELISA. </li><li>Bachelor's, Master's, or PhD in pharmaceutical chemistry or a related field. </li><li>Ability to independently execute laboratory assays and perform data reviews. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Experience in assay development, method validation, method development, and method transfer. </li><li>Familiarity with quality control and LIMS. </li><li>Knowledge of immunoassays. </li></ul> <p>Work Environment</p> <p>This is a large pharmaceutical manufacturing organization focused on vaccine and mAb intermediate manufacturing. The position involves working in both office and lab environments. The work schedule is 1st Shift, Monday through Friday, from 8 AM to 5 PM, with occasional weekend work required on a rotating basis. The company is committed to innovation and quality, offering opportunities to work on high-profile projects and gain training in diverse methods.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $40.00 - $55.00/hr.</p> <p>Eligibility requirements apply to some benefits and may depend on your job</p> <p>classification and length of employment. Benefits are subject to change and may be</p> <p>subject to specific elections, plan, or program terms. If eligible, the benefits</p> <p>available for this temporary role may include the following:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <p>Workplace Type</p> <p>This is a fully onsite position in Raleigh,NC.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Aug 22, 2025.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>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 actalentaccommodation@actalentservices.com for other accommodation options.</p>