Job Information
Actalent Scientist in Wilson, North Carolina
Job Title: Senior ScientistJob Description
A pharmaceutical company specializing in sterile injectable products is seeking a Senior Scientist to join their team. The Senior Scientist will coordinate and lead the method transfer, method verification, and co-validation of compendial and non-compendial analytical methods. This role involves planning and coordinating method transfer and method verification activities from the Innovation & Development (I&D) department or between facilities to the Quality Control laboratory. As a subject matter expert, the Senior Scientist will also support the critical tests associated with new product launches and ensure conformance of the release and stability profile as documented in development reports and regulatory submissions.
Responsibilities
Coordinate and execute method transfers, method verifications, and co-validations of testing procedures within the Quality Control laboratory.
Review results and verification reports following method transfers and verification protocols.
Act as liaison between I&D departments or Production Units and the QC Chemistry laboratory for new testing procedures.
Serve as a subject matter expert for critical tests supporting new product launches.
Identify and investigate complex problems occurring in QC laboratories and provide technical support for resolution.
Prepare documentation for regulatory submissions as required.
Review, update, and approve documentation such as protocols, test methods, SOPs, and raw material/finished product specifications.
Participate in the orientation and training of laboratory employees in new analytical method techniques.
Establish work priorities and ensure assignments are completed on schedule.
Function as an analytical project leader in inter-departmental meetings.
Interface with Plant Operations and Technical Transfer personnel to resolve plant technical issues requiring analytical expertise.
Essential Skills
Minimum of 8 years of experience within pharmaceuticals, particularly in GMP environments.
Extensive experience with HPLC, GC, FTIR, UV-Vis, Karl-Fisher, and spectroscopic methods.
Critical experience with ICP-MS.
Proficiency in method transfer and validation, including writing protocols for method transfers and validation reports.
Strong technical writing skills.
Additional Skills & Qualifications
- Experience with coagulation analyzer and chromogenic assay.
Work Environment
The position is an on-site laboratory role requiring practical knowledge of analytical chemistry. The standard work shift is from 8 AM to 5 PM. The role reports to the Analytical Services manager and involves independent execution of non-routine and complex analytical methodologies within the Quality Control laboratory. The company is rapidly expanding its manufacturing capabilities and developing new products, including prefilled syringes and more complex molecules in IV bags.
Job Type & Location
This is a Contract position based out of Wilson, NC.
Pay and Benefits
The pay range for this position is $50.00 - $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)
Workplace Type
This is a fully onsite position in Wilson,NC.
Application Deadline
This position is anticipated to close on Mar 16, 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 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.
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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.