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30 days
Not Specified
Not Specified
$27.06/hr - $49.91/hr (Estimated)
<p>Job Title: Scientist</p> <p>Responsibilities</p> <ul> <li>Coordinate and execute method transfers, method verifications, and co-validations of testing procedures within the Quality Control laboratory. </li><li>Review results and verification reports following the execution of method transfers and verification protocols. </li><li>Serve as a liaison between departments for the transfer and implementation of new testing procedures. </li><li>Act as a subject matter expert for critical tests supporting new product launches. </li><li>Identify and investigate complex problems in QC laboratories, providing technical support for resolution. </li><li>Prepare and review documentation for regulatory submissions, including protocols, test methods, and SOPs. </li><li>Participate in the orientation and training of laboratory employees in new analytical methods. </li><li>Handle complex projects with general guidance, establishing work priorities and ensuring assignments are completed on schedule. </li><li>Function as an analytical project leader in inter-departmental meetings. </li><li>Interface with Plant Operations and Technical Transfer personnel to resolve plant technical issues. </li></ul> <p>Essential Skills</p> <ul> <li>Minimum of 8 years of experience in the pharmaceutical industry with a strong foundation in a GMP setting. </li><li>Proficiency in analytical techniques such as HPLC, GC, FTIR, UV-Vis, and Karl-Fisher. </li><li>Experience with method transfer, method validation, and writing of protocols. </li><li>Technical writing skills for creating validation reports and documentation. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Experience with Coagulation Analyzer: Chromogenic Assay. </li><li>Broad knowledge of analytical chemistry, pharmaceutical development, and regulatory requirements. </li></ul> <p>Work Environment</p> <p>This is an on-site laboratory position with normal first shift hours, 8 AM to 5 PM. The role requires practical knowledge of analytical chemistry and is not part of the QC team, but focuses on method transfer. The work environment is dynamic, with ongoing growth in manufacturing capabilities and the introduction of new products, including prefilled syringes and more complex molecules.</p> <p>Job Type & Location</p> <p>This is a Contract position based out of Wilson, NC.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $50.00 - $50.00/hr.</p> <p>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)</p> <p>Workplace Type</p> <p>This is a fully onsite position in Wilson,NC.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Mar 16, 2026.</p> <p>About Actalent</p> <p>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.</p> <p>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.</p> <p>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 for other accommodation options.</p>
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