Senior Scientist

Sr Scientist Job Description A pharmaceutical company specializing in sterile injectable products is seeking a Sr Scientist to join their team. The Sr 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 Sr 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 Apr 6, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.