<p>Job Title: Stability Support SpecialistJob Description</p> <p>The Stability Support Specialist is responsible for supporting the evaluation, alignment, and remediation of stability programs within a regulated pharmaceutical environment. The role focuses on performing gap assessments of local and global stability SOPs, evaluating stability chambers and studies, and identifying product placement needs and redundancies to ensure compliance, business continuity, and inspection readiness. The specialist will work cross-functionally with QC, QA, and Stability teams to assess current practices, document gaps, and support improvements to stability program governance and execution.</p> <p>Responsibilities</p> <ul> <li>Conduct gap assessments of local site SOPs against global stability SOPs and regulatory expectations. </li><li>Identify inconsistencies, gaps, or missing controls related to stability study management, chamber operation, and data handling. </li><li>Document findings and support the development of remediation or alignment plans in collaboration with Quality and Stability leadership. </li><li>Assess stability chambers to ensure alignment with approved SOPs, qualification status, and intended use. </li><li>Review chamber utilization, monitoring practices, alarm management, and contingency plans. </li><li>Support evaluation of chamber capacity and redundancy to mitigate risk to ongoing and future stability studies. </li><li>Review existing stability studies to confirm appropriate product placement within stability chambers. </li><li>Identify gaps in product coverage, including missing studies or insufficient redundancy across chambers or sites. </li><li>Support identification of critical products requiring backup placement to reduce risk of data loss or chamber failure. </li><li>Ensure stability program activities align with GMP requirements, regulatory guidance, and internal quality standards. </li><li>Support updates to stability-related documentation, including SOPs, work instructions, and tracking tools. </li><li>Assist with preparation for internal audits and regulatory inspections by ensuring stability documentation is complete and defensible. </li><li>Partner with QC, QA, Engineering, and Stability SMEs to assess current state and implement improvements. </li><li>Communicate findings clearly and concisely to stakeholders and support follow-up actions. </li><li>Contribute to continuous improvement initiatives within the stability program. </li></ul> <p>Essential Skills</p> <ul> <li>Previous pharmaceutical experience with GMP standards. </li><li>Experience in understanding stability studies and being a stability program SME. </li><li>Experience running a gap assessment for critical stability programs. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Experience with stability savings programs. </li></ul> <p>Work Environment</p> <p>The role is based on-site in Wilson and operates during normal business hours. However, availability to assist in training night shifts on some days is required. The work takes place in a lab space, within a DEA and GMP controlled environment.</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 - $60.00/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 17, 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>