Job Description Our Client is seeking a talented and experienced Scientist to join the Quality Control Method Transfer and Validation team. The successful candidate will perform method validation activities, including drafting protocols and reports, executing validation assays, and conducting data analysis. The role involves ensuring adherence to cGMP standards and data integrity principles. Responsibilities
- Independently conceptualize, plan, and execute laboratory experiments.
- Collaborate with colleagues and subject matter experts to determine suitable analytical methodologies for project initiatives.
- Lead and manage multiple projects, assisting teams in developing effective strategies for analytical needs and controls.
- Engage with the method development team for 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 as required.
- Independently analyze experimental data and provide conclusive insights.
- Mentor junior scientists and offer technical guidance as needed.
- Support technical leads and the Sr. Scientist with project activities to meet deadlines.
- Experience with GMP, ELISA, Slot BLOT, Spectramax, and Nephelometry.
- Relevant industry experience in pharmaceutical chemistry.
- Ability to independently execute laboratory assays and draft protocol deviations under supervision.
- Perform thorough data reviews.
- Bachelor's, Master's, or PhD in a related field with applicable relevant experience.
- Experience in assay development, method validation, method development, and method transfer.
- Understanding of cGMP and quality control processes.
- Proficiency with LIMS and immunoassays.
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 Aug 29, 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.
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