Scientist - Plate Based

This role supports a Quality Control laboratory within a GMP-regulated pharmaceutical manufacturing environment, with a primary focus on biologics-related plate-based analytical testing. The Scientist will lead and support the transfer, qualification, and validation of analytical methods for new products entering the site, ensuring robust, compliant implementation into routine QC operations. The position offers the opportunity to work on high-profile projects, gain exposure to a wide range of analytical methods and technologies, and contribute directly to the delivery of safe and effective products to patients within a science- and risk-based quality culture.

• Support the transfer, qualification, and validation of analytical methods associated with new product introductions into the site.
• Execute method transfer studies, assay qualification protocols, and validation activities in accordance with GMP and internal procedures.
• Assist with preparation and execution of technical protocols, including drafting, reviewing, and finalizing method transfer and validation documents.
• Perform analytical testing using ELISA, plate-based assays, SoloVPE, Slot Blot, and SDS-PAGE to support product release, stability, and characterization activities.
• Analyze test results, interpret data, and ensure accuracy, completeness, and integrity of all analytical outputs.
• Troubleshoot assay performance issues, identify root causes, and support or lead laboratory investigations as needed.
• Support implementation of new testing methods into routine QC operations, including method training and execution support for other analysts.
• Maintain GMP-compliant laboratory records, including contemporaneous documentation of all testing activities and results.
• Review analytical data for completeness, accuracy, and adherence to data integrity principles, including compliance with cGMP and GDP standards.
• Ensure adherence to relevant quality standards, regulatory requirements, and internal policies in all laboratory activities.
• Support inspection readiness efforts by maintaining organized documentation and participating in audits or inspections as required.
• Partner with cross-functional teams such as Quality Control, Quality Assurance, Validation, and Technical Operations to support project timelines and product transfer activities.
• Participate in technical discussions and method transfer meetings, providing scientific input and data-based recommendations.
• Contribute to continuous improvement initiatives within the laboratory, including optimization of methods, workflows, and documentation practices.
• Engage in knowledge sharing and collaboration with colleagues to promote a dynamic, learning-focused laboratory environment.

• Bachelor's degree in Biology, Biochemistry, Biotechnology, Microbiology, Chemistry, or a related scientific discipline.
• 3 years of experience working in a GMP-regulated pharmaceutical, biotechnology, or biologics laboratory environment.
• Hands-on experience performing ELISA assays in a Quality Control or similar regulated setting.
• Hands-on experience with plate-based assays, including setup, execution, and data analysis.
• Hands-on experience using SoloVPE for analytical measurements.
• Hands-on experience with Slot Blot assays.
• Experience supporting method transfer, qualification, or validation activities for analytical methods.
• Strong understanding of GMP documentation practices and regulatory requirements for QC laboratories.
• Ability to maintain GMP-compliant laboratory records and adhere to cGMP and GDP principles.
• Demonstrated ability to analyze and interpret analytical data with a high level of accuracy and attention to detail.
• Experience troubleshooting assay performance and supporting laboratory investigations.
• Strong communication and collaboration skills to work effectively with cross-functional teams in a regulated environment.

• 5 years of experience in the pharmaceutical or biologics industry, particularly in Quality Control or analytical laboratories.
• Experience supporting new product introductions, including assay transfer and validation programs.
• Familiarity with SDS-PAGE, including sample preparation, gel running, and data interpretation.
• Experience using LIMS or other electronic laboratory systems for sample management and data recording.
• Experience working with biologics, vaccines, monoclonal antibodies, or protein-based products in a QC or analytical context.
• Exposure to or experience within environments focused on vaccine and monoclonal antibody intermediate manufacturing.
• Demonstrated ability to contribute to continuous improvement initiatives and process optimization in a laboratory setting.
• Interest in learning new analytical methods and technologies and expanding technical expertise over time.

The role is based within a large pharmaceutical manufacturing organization focused on vaccine and monoclonal antibody intermediate manufacturing, with a strong emphasis on quality, safety, and patient impact. The position is primarily laboratory-based, with the individual working almost 100% of the time in an office and lab environment that supports GMP-regulated QC testing. The standard schedule follows a first-shift, Monday through Friday workweek, with core hours aligned to an 8:30 a.m. start time. Team members are expected to attend a daily tier meeting at 8:30 a.m., and any changes to shift timing are coordinated with the team lead and collaborating analysts. The environment is highly dynamic and innovation-driven, offering exposure to high-profile projects, new methods, and advanced technologies. The culture emphasizes a science- and risk-based, compliant quality mindset that is flexible, innovative, and customer oriented, where contributions in development, maintenance, compliance, and analysis directly impact patients.

This is a Contract position based out of Sanford, NC.

The pay range for this position is $30.00 - $60.00/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)

This is a fully onsite position in Sanford,NC.

This position is anticipated to close on Aug 13, 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.

Salary : $30 - $60