Scientist, AnalyticalMake an Impact on Patient Health Through Cutting-Edge Analytical Science Are you a passionate analytical scientist looking to apply your expertise in a dynamic pharmaceutical environment? Join our team and play a pivotal role in advancing life-changing therapies by supporting analytical method validation, transfer, development, and quality control activities. As an Analytical Scientist, you will be a key contributor within the Quality Control Method Transfer & Validation organization, leading critical laboratory studies that ensure the reliability, robustness, and regulatory compliance of analytical methods used to support pharmaceutical manufacturing. This role offers the opportunity to work with advanced analytical technologies, collaborate with cross-functional scientific teams, and directly influence product quality and patient outcomes. If you thrive in a fast-paced, highly collaborative environment where science drives innovation, we'd love to hear from you. What You'll DoAnalytical Leadership & Scientific Execution + Design, plan, and execute complex analytical studies supporting method validation, method transfer, assay development, and quality control testing. + Independently perform laboratory experiments, analyze results, and provide scientifically sound conclusions and recommendations. + Support product transfers through in-process and final product analytical testing. + Identify opportunities to enhance method performance, efficiency, and reliability. Method Validation & Technology Transfer + Lead method validation and transfer activities from protocol development through execution and final report generation. + Author validation protocols, reports, technical documentation, and supporting regulatory documentation. + Collaborate closely with method development, manufacturing, quality, and technical teams to ensure successful technology transfers. + Evaluate and implement new analytical techniques, instrumentation, and scientific approaches when appropriate. Data Analysis & Compliance + Review and interpret analytical data while ensuring compliance with cGMP requirements and data integrity standards. + Utilize scientific software, chromatography data systems, and data visualization tools to support data-driven decision-making. + Ensure all documentation, reports, and laboratory records meet regulatory and quality expectations. Collaboration & Mentorship + Partner with cross-functional teams to develop analytical strategies and project timelines. + Provide technical guidance and mentorship to junior scientists and laboratory personnel. + Support project prioritization and contribute to the successful completion of key organizational objectives. Continuous Improvement + Drive improvements in analytical procedures, workflows, and laboratory documentation. + Contribute to the expansion of analytical capabilities through innovative thinking and scientific problem-solving. + Support a culture of operational excellence, quality, and continuous learning. What We're Looking ForRequired Qualifications + Bachelor's, Master's, or PhD in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline. + Industry experience in pharmaceutical, biotechnology, or related regulated laboratory environments. + Experience working within cGMP-regulated environments and a strong understanding of quality systems and data integrity principles. + Hands-on experience with: + HPLC/UPLC systems (including Waters platforms) + Empower Chromatography Data Software + Capillary Electrophoresis (CE, PA 800, or similar systems) + Plate-based analytical or chemistry assays + Demonstrated experience with method validation, method transfer, and technical report writing. + Strong analytical thinking, problem-solving, and data interpretation skills. + Ability to manage multiple priorities in a deadline-driven environment while maintaining scientific rigor and attention to detail. Preferred Qualifications + Experience in analytical method development and assay development. + Familiarity with LIMS and laboratory data management systems. + Experience using Maurice or other advanced capillary electrophoresis platforms. + Exposure to pharmaceutical manufacturing, biologics, vaccines, or monoclonal antibody programs. + Experience with data visualization, predictive modeling, or computational analytical tools. + Prior experience mentoring scientists or providing technical leadership on projects. Why Join Us?

Meaningful Work Contribute directly to the development and manufacture of innovative medicines, vaccines, and biologic therapies that improve and save lives around the world. Advanced Science & Technology Work with leading-edge analytical instrumentation and technologies while expanding your expertise across multiple analytical platforms and methodologies. Career Growth Gain exposure to method development, validation, transfer, compliance, quality systems, and cross-functional project leadership. We invest in continuous learning and professional development. Collaborative Culture Join a team of talented scientists who value innovation, knowledge-sharing, scientific excellence, and continuous improvement. High-Impact Projects Be part of critical pharmaceutical manufacturing programs where your scientific contributions influence product quality, regulatory compliance, and patient outcomes. Work Environment This position is based within a state-of-the-art pharmaceutical manufacturing organization focused on vaccines and monoclonal antibody production. The role combines laboratory and office-based work in a collaborative scientific environment that continues to evolve through ongoing facility and laboratory expansion. Standard hours are Monday through Friday, with flexibility to support critical testing activities and operational priorities. Alternative schedules may occasionally be available based on business needs. Join Us If you're excited by complex analytical challenges, passionate about scientific excellence, and motivated by the opportunity to make a meaningful impact on patient health, we encourage you to apply and become part of our growing team. Job Type & Location This is a Contract position based out of Sanford, NC. Pay and Benefits The pay range for this position is $35.00 - $65.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. 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 Aug 31, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.