What are the responsibilities and job description for the Manufacturing Associate, Sterile Injectables position at Kelly?
Kelly® Science & Clinical is seeking Manufacturing Associates for a direct-hire opportunity with a leading specialty pharmaceutical company at its facilities in Morrisville, NC, or Charleston, SC. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and medical device industries.
Workplace: Onsite in Morrisville, NC, or Charleston, SC.
Position Title: Manufacturing Associate, Sterile Injectables
Position Type: Direct hire
Pay rate range $25-35 per hour
Work schedule
- Monday-Friday (Some OT/Flex Required)
- 2nd Shift: 3:00 pm – 11:30 pm
- 3rd Shift: 11:00 pm – 7:00 am
Be a part of the team that delivers life-saving therapies.
About the Opportunity:
Are you passionate about pharmaceutical manufacturing and ready for your next challenge in a dynamic, state-of-the-art sterile injectables environment? Kelly Science and Clinical is seeking skilled Manufacturing Technicians (Levels II & III) to join our rapidly expanding team focused on the production of high-quality sterile vial and syringe products for both clinical and commercial markets.
This is a hands-on, advanced role in a world-class, cGMP-compliant facility, where excellence, precision, and teamwork define success. You'll work with cutting-edge technology and have opportunities for growth in a supportive environment committed to career advancement.
What You'll Do:
- Lead and execute critical manufacturing processes including compounding, aseptic filling using isolators, stoppering, capping, and rigorous visual inspection of sterile injectable products.
- Accurately perform in-process sampling, weight verification, component counting, and calculations to ensure compliance with strict batch requirements.
- Complete and maintain clear and concise documentation, batch records, and reports in strict alignment with GMP, GDP, and SOP standards.
- Operate, troubleshoot, and maintain specialized sterile manufacturing equipment to ensure uninterrupted production.
- Uphold and promote best-in-class aseptic techniques, PPE practices, and contamination control always.
- Partner cross-functionally to support process improvement projects and actively escalate issues to maintain the highest product quality standards.
- Embrace ongoing learning, cross-training, and skill development as you grow your career within the organization.
- Flexibility to work occasional overtime or weekends as production needs arise.
What You Bring:
- High school diploma or GED required; Associate's or Bachelor’s degree in a scientific or technical field preferred.
- For Technician II: 2 years’ experience in sterile manufacturing or a highly regulated setting.
- For Technician III: 3–5 years’ relevant experience preferred.
- Demonstrated skills in aseptic filling, compounding, or visual inspection within the pharmaceutical industry.
- In-depth knowledge of cGMP regulations, GDP, and SOP-driven processes.
- Exceptional attention to detail, organizational excellence, and proven problem-solving ability.
- Ability to thrive in a fast-paced, team-driven environment with a proactive and adaptable approach.
Your Pathway to Career Advancement:
We invest in our people. Technicians who demonstrate proficiency, initiative, and leadership may advance rapidly to senior, lead, or supervisory roles. Continual skill development and cross-training are key parts of our culture.
Ready to make a difference in sterile manufacturing? Join us and be part of the future of pharmaceuticals
Salary : $25 - $35