Manufacturing Associate 3 – Column Packing Position Available In Wake, North Carolina
Tallo's Job Summary: The Manufacturing Associate 3 - Column Packing role at Diosynth Biotechnologies involves leading and executing manufacturing processing steps in a 24/7 operational facility. Responsibilities include process monitoring, in-process testing, and validation protocols. The position requires shift work and a high school diploma with 4 years of related experience. Diosynth Biotechnologies is seeking passionate individuals to contribute to life-changing biopharmaceutical manufacturing.
Job Description
Manufacturing Associate 3 – Column Packing
Job Locations
US-NC-Holly Springs
Posted Date
2 days ago
(4/17/2025 5:55 PM)
Requisition
ID 2025-34179
Category Manufacturing Company (Portal Searching) Diosynth Biotechnologies
Position This role will lead and execute manufacturing processing steps and associated activities. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. Company Follow Your Genki to North America’s largest, state-of-the-art Life Science Manufacturing Facility & CDMO The work we do at Diosynth Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join Diosynth Biotechnologies and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharmapanies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive – what we call Genki. Join us We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America. The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States.
Job Description What You’ll Do During Project Phase:
Contribute to the preparation for operational readiness related to bulk drug substance manufacturing
Possible assignments include: Supporting projects related to – Procedure review and/or creation, development or transfer of manufacturing business processes, testing andmissioning support
Travel up to 0-25% (international or domestic) may be required
In Operations:
Lead, execute and document manufacturing processing steps and/or manufacturing support activities: Process monitoring and control
Perform in-process testing (pH, conductivity, visual inspection)
Execute validation protocols according to cGMP Standard Operating Procedures (SOPs)
Maintain training to perform all required manufacturing activities
Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area
This role requires shift work (weekend and potential for nights)
Perform other duties as assigned Who You Are You have the ability to assist in troubleshooting. You have strong verbal and writtenmunication skills. You have knowledge of the operation of production equipment in their respective unit operation. You have a basic understanding of manufacturing run cadence and order of shift activities. You are knowledgeable in cGMP, safety and operational procedures. You have the ability to work in a team environment. Basic Requirements High School Diploma or GED
4 years of related experience in a manufacturing environment Preferred Requirements Associate’s Degree OR
BA/BS, preferably in Life Sciences or Engineering
Associate’s Degree + 2 years of related experience in a cGMP manufacturing environment OR
Equivalent Military training or experience
Qualified experience on unit operation (DPFG Filler or Cell Culture – Seed Train)
BioWorks or BTEC Capstone cGMP coursework preferred
WORKING CONDITIONS & PHYSICAL REQUIREMENTS
Be exposed to an environment that may necessitate respiratory protection
Be exposed to noisy environments
Have a normal range of vision
Climb ladders and stairs of various heights
Experience prolonged sitting, standing, walking, bending, stooping and stretching throughout the shift, up to 12 hours
Use hand-eye coordination and manual dexterity sufficient to operate aputer keyboard, telephone, calculator, and other office equipment is required
May be required to lift up to 50 pounds on occasion