Manufacturing Associate
Job
Actalent
Wilson, NC (In Person)
Full-Time
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Job Description
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Manufacturing Associate Job Description This role supports sterile, aseptic fill‑finish operations for prefilled syringe manufacturing on isolator‑based production lines within a pharmaceutical environment. The Manufacturing Associate executes GMP manufacturing activities, operates isolator equipment, and upholds product quality, safety, and regulatory compliance. This position is ideal for someone with hands‑on experience in sterile manufacturing who understands the critical nature of aseptic processing and is eager to grow through cross‑training and development opportunities. Responsibilities Operate and monitor isolator‑based fill‑finish equipment used in the production of prefilled syringes. Perform aseptic operations, including component preparation and staging for production runs. Set up production lines and perform line changeovers in accordance with established procedures. Carry out filling, stoppering, and capping activities for prefilled syringe products while maintaining aseptic technique. Execute manufacturing processes in strict accordance with cGMPs, standard operating procedures (SOPs), batch records, and safety requirements. Perform routine in‑process checks and visual inspections to ensure product quality and process control. Complete accurate and timely documentation, including batch records, logbooks, and entries in electronic systems. Support environmental monitoring activities and consistently maintain proper aseptic technique. Identify and promptly escalate deviations, equipment issues, or process abnormalities to supervision and quality teams. Participate in deviation investigations, root cause analysis, and corrective and preventive action (CAPA) activities as required. Maintain cleanroom standards, including successful gowning qualification and housekeeping of classified areas. Collaborate with cross‑functional teams such as Quality, Engineering, and Maintenance to support continuous and reliable operations. Contribute to continuous improvement initiatives focused on enhancing safety, quality, and operational efficiency. Essential Skills Hands‑on experience in sterile or aseptic manufacturing environments, preferably on isolator‑based production lines. Strong understanding of aseptic processing principles and sterile operations. Knowledge of and adherence to current Good Manufacturing Practices (cGMP). Ability to follow SOPs, batch records, and safety requirements with high attention to detail. Capability to perform aseptic gowning and maintain aseptic technique in cleanroom environments. Competence in completing accurate, legible, and timely GMP documentation. Ability to recognize and escalate deviations, equipment issues, or process abnormalities. Comfort working cross‑functionally with Quality, Engineering, Maintenance, and other operational teams. Additional Skills & Qualifications GMP‑related training or certification, such as a bioworks or similar GMP certification. Previous experience in GMP aseptic manufacturing or sterile processing. Familiarity with environmental monitoring practices in cleanroom settings. Experience participating in deviation investigations, root cause analysis, and CAPA activities. Interest in cross‑training and developing broader manufacturing skills within a sterile pharmaceutical environment. Work Environment This is an on‑site role based in Wilson, North Carolina, working in a sterile pharmaceutical manufacturing facility with classified cleanroom areas and isolator‑based production lines. The position follows a night shift schedule on a 2‑3‑2 rotation, providing consistent, structured hours. Work is performed in a controlled environment that requires proper gowning and adherence to cleanroom protocols. The site produces pharmaceutical products that are critical to hospitals and patients across the United States and offers cross‑training opportunities, exposure to multiple manufacturing operations, and a culture that supports learning and development. Job Type & Location This is a Contract position based out of Wilson, NC. Pay and Benefits The pay range for this position is $23.50 - $23.50/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.
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