Scientist

Job Title:

Scientist Job Description A pharmaceutical company specializing in sterile injectable products is seeking a dedicated Scientist to join their team. The role involves leading the planning and coordination of method transfer and method verification activities, crucial for transferring analytical methods from the Innovation & Development department or between facilities to the Quality Control laboratory. The Scientist will play a key role in new product launches by becoming the expert within the Quality Control organization for critical tests. Responsibilities Coordinate and execute method transfers, method verifications, and co-validations of testing procedures within the Quality Control laboratory. Analyze organic and inorganic compounds to determine chemical and physical properties, composition, structure, relationships, and reactions. Execute verification protocols to verify vendor and USP analytical methods. Review obtained results and verification reports following method transfers and verification protocols. Serve as a liaison between I&D departments or Production Units and the QC Chemistry laboratory for transferring and implementing new testing procedures. Act as a subject matter expert for critical tests supporting new product launches. Identify and investigate complex problems 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. Handle complex projects with general guidance, 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 technical issues requiring analytical support. Essential Skills Minimum of 8 years of experience in pharmaceuticals with a strong understanding of GMP. Proficiency in HPLC, GC, FTIR, UV-Vis, Karl-Fisher, and spectroscopic methods. Experience with method verification and validation. Strong troubleshooting skills in analytical chemistry. Additional Skills & Qualifications Sound chemistry experience with examples of troubleshooting. Open to learning and developing skills in protocol writing and validation. Experience with Coagulation Analyzer and Chromogenic Assay is advantageous. Work Environment The role follows a normal 1st shift schedule, from 8 AM to 5 PM. The position reports to the Analytical Services manager but is not part of the QC team. The work environment is dynamic, with the site rapidly growing its manufacturing capabilities, moving towards more complex molecules in IV bags, including heparin, chemo drugs, and antibiotics. There is a strong focus on career development opportunities, offering a chance to grow as a scientist. Job Type & Location This is a Contract position based out of Wilson, NC. Pay and Benefits The pay range for this position is $40.00 - $50.00/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 Jun 1, 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 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.