Manufacturing Technicians (Science) Position Available In Wake, North Carolina
Tallo's Job Summary: Manufacturing Technicians (Science) are needed for Sterile Injectable Operations at a Morrisville, NC site, with pay up to $35/hour. Responsibilities include aseptic processing, equipment maintenance, and process improvements in a GMP-compliant setting. Ideal candidates have sterile pharmaceutical manufacturing experience, attention to detail, and can work independently in a cleanroom environment.
Job Description
Position:
Manufacturing Technician –
Sterile Injectable Operations Location:
Morrisville, NC Pay Rate:
Up to $35/hour (based on experience)
Overview:
A fast-paced, regulated manufacturing site is seeking an experienced Manufacturing Technician to support sterile injectable operations. This role involves hands-on aseptic processing, equipment setup and maintenance, and participation in process improvements within a GMP-compliant environment. The ideal candidate will have a background in sterile pharmaceutical manufacturing, strong attention to detail, and the ability to operate with minimal supervision in a cleanroom setting.
Key Responsibilities:
Perform sterile production operations including material handling, compounding, aseptic filling, lyophilization, capping, and visual inspection under strict GMP and safety protocols. Lead or assist with equipment setup, troubleshooting, preventative maintenance, and cleaning validation. Execute batch records, SOPs, and controlled documentation with a focus on accuracy, compliance, and right-first-time execution. Serve as a technical SME for aseptic processes and provide mentorship or training to team members as needed. Support cross-functional teams in equipment qualification, process validation, and deviation investigations. Participate in routine sampling, in-process checks, and quality inspections to ensure product meets required specifications. Perform routine room and equipment cleaning/sanitation in accordance with environmental monitoring and contamination control standards. Collaborate with QA, Engineering, and Technical Operations to identify and implement process improvements. Take part in shift handovers, daily huddles, and safety discussions to ensure smooth operation and knowledge transfer.
Qualifications:
High school diploma or GED required; Associate or Bachelor’s degree in a scientific or technical discipline preferred. Minimum 5 years of experience in GMP manufacturing, preferably with expertise in sterile/aseptic processing or biologics production. Strong working knowledge of cleanroom protocols, gowning, aseptic technique, and contamination control. Experience with at least some of the following technologies: autoclave prep, vial washing, compounding, isolator filling, lyophilization, visual inspection, or documentation review. Ability to interpret batch records and SOPs; experience suggesting or implementing procedural improvements is a plus. Effective communication and leadership skills; prior experience training or mentoring peers preferred. Capable of lifting up to 30 lbs and wearing full PPE, including respirators, when required. 9775493