Pharmaceutical Assembly Jobs in Raleigh, NC (NOW HIRING)

During the project phase, you will:

• Serve as a key contributor for operational readiness in bulk drug substance manufacturing.
• Support commissioning and qualification of equipment.
• Create and/or review procedures and SOPs.
• Help onboard manufacturing staff and transfer or develop manufacturing business processes.
• Support new item creation and singleuse assembly transfer or design.

In routine operations, you will:

• Champion a strong safety culture and strictly follow EHS protocols.
• Lead, execute, and document manufacturing processing steps and support activities within your functional area, ensuring adherence to SOPs and cGMP regulations.
• Monitor and control processes, performing and/or overseeing inprocess testing (pH, conductivity, visual inspections).
• Execute validation protocols per cGMP SOPs and provide approvals as a backup to the supervisor.
• Maintain all required training and qualifications; train and mentor junior associates to elevate team capabilities.
• Support daily floor scheduling and act as a backup to the supervisor as needed.
• Lead troubleshooting for operational issues to restore steadystate production.
• Assist the supervisor with shift huddles, tiered escalations, investigations, and continuous improvement projects.
• Serve as area lead for cycle counts and materials management.
• Perform other duties as assigned to meet production goals.

Minimum education and experience (one of the following):

• High school diploma or GED with 8 years of experience in life sciences manufacturing, OR
• Associate degree with 6 years of experience in life sciences manufacturing, OR
• BA/BS, preferably in Life Sciences or Engineering, with 4 years of experience in life sciences manufacturing, OR
• Equivalent military experience.

Plus:

• Proficient understanding of cGMP regulations and pharmaceutical industry standards.
• Fully qualified in a functional area (e.g., Drug Product Formulation and Filling, Weigh and Dispense, Cell Culture, or Purification) and subjectmatter expertise across all unit operations within that area (e.g., Inoculation, Seed Train, Production Bioreactor).

Preferred:

• Bioworks Certification.

• Make a direct impact on patients by ensuring reliable, compliant manufacturing of critical therapies.
• Work with stateoftheart technologies and singleuse systems in a collaborative, safetyfirst environment.
• Grow your leadership skills by mentoring others and acting as a backup to the supervisor.

Ready to lead on the manufacturing floor and help bring our facility to life? Apply today.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

*#LI-Onsite