Manufacturing Associate

Job Title: Manufacturing Associate Job Description A sterile manufacturer of pharmaceutical products is seeking a team of Manufacturing Associates. The Manufacturing Associate will support aseptic fill-finish operations for prefilled syringe manufacturing within isolator-based production lines. This role is responsible for executing GMP manufacturing activities, operating isolator equipment, and ensuring product quality, safety, and compliance with all regulatory and internal standards. Responsibilities + Operate and monitor isolator-based fill-finish equipment used in the production of prefilled syringes. + Perform aseptic operations including component preparation and staging, line setup and changeovers, and filling, stoppering, and capping activities. + Execute manufacturing processes in accordance with cGMPs, SOPs, batch records, and safety requirements. + Perform routine in-process checks and inspections to ensure product quality and process control. + Complete accurate and timely documentation, including batch records, logbooks, and electronic systems. + Support environmental monitoring activities and maintain aseptic technique at all times. + Identify and escalate deviations, equipment issues, or process abnormalities to supervision and quality teams. + Participate in deviation investigations, root cause analysis, and CAPA activities as required. + Maintain cleanroom standards, including gowning qualification and housekeeping of classified areas. + Collaborate with cross-functional teams including Quality, Engineering, and Maintenance to support continuous operations. + Support continuous improvement initiatives focused on safety, quality, and efficiency. Essential Skills + Hands-on experience in sterile manufacturing environments, specifically working on isolator lines. + Understanding of aseptic processing and aseptic gowning. + Experience with GMP - bioworks certification or previous GMP aseptic manufacturing experience. Additional Skills & Qualifications + Strong commitment to maintaining aseptic technique and cleanroom standards. + Ability to identify and escalate deviations and participate in investigations. + Collaborative skills for working with cross-functional teams. Work Environment The role operates on a night shift schedule, following a 2-3-2 pattern. Employees will work in a sterile pharmaceutical manufacturing environment, focusing on producing critical products for the hospital system and patients across the US. The opportunity offers cross-training for professional development and growth in manufacturing experience. Job Type & Location This is a Contract to Hire position based out of Wilson, NC. Pay and Benefits The pay range for this position is $22.00 - $24.00/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: u2022 Medical, dental & vision u2022 Critical Illness, Accident, and Hospital u2022 401(k) Retirement Plan u2013 Pre-tax and Roth post-tax contributions available u2022 Life Insurance (Voluntary Life & AD&D for the employee and dependents) u2022 Short and long-term disability u2022 Health Spending Account (HSA) u2022 Transportation benefits u2022 Employee Assistance Program u2022 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 10, 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 ( ) for other accommodation options.

Created: 2026-02-26