Job Title:

Quality Control / Analytical Development SpecialistJob Description In this role, you will be instrumental in developing analytical methods, characterizing proteins, and assisting in the formulation development and stability programs for drug substances and drug products. You will collaborate with a team to enhance analytical and formulation development as well as stability processes. This laboratory position requires a hands-on approach and the ability to work independently while reporting to an Analytical Scientist. Familiarity with GxP lab practices, including good documentation practices, is essential. Routine analytical testing in a quality-regulated environment is also part of this position. Responsibilities + Perform analytical sample analysis to support process development using techniques such as ELISA, HPLC, and UV-Vis. + Utilize tools like Empower and Waters/Thermo Fisher HPLCs, and plate readers. + Aid in analytical testing for release and stability testing of drug substances, intermediates, and drug products. + Assist in drafting test methods for routine sample analysis. + Identify analytical science capabilities and technology tools necessary for research, manufacturing, process development, QC testing, and new drug candidate formulation development. + Maintain and organize the laboratory environment, including samples, reagents, and instruments. + Support analytical method transfer, qualification, and validation for commercial QC and contract laboratories as needed. + Develop scientifically sound, data-driven specifications. + Prepare and deliver technical reports, documents, batch analyses, analytical methods, and reference standards for regulatory submissions. Essential Skills + Knowledge of cGMP, GxP, and analytical instrumentation. + Experience in analytical method development, transfer, qualification, and validation. + Experience applying GxP/GLP/GMP standards based on project and sample type with a risk-based compliance mindset. + Proficiency with multi-instrument analytical techniques (HPLC, ELISA, plate-based assays) in fast-paced, multi-project environments. Additional Skills & Qualifications + A passionate, go-getter attitude that thrives in a fast-paced, team-oriented environment. + Experience in handling multiple projects with varying levels of GLP simultaneously is preferred. + Applicable professional experience is preferred over educational background, with consideration for candidates with an Associate degree. Work Environment The work environment is fast-paced and team-oriented, where collaboration and adaptability are key. Job Type & Location This is a Contract position based out of Durham, NC. Pay and Benefits The pay range for this position is $40.00 - $45.00/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 Durham,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.