Biotech Manufacturing Associate (II–V)

FUJIFILM Biotechnologies; Holly Springs (NC); On-site; USD 42,000 - 54,000; Full time

Job summary

FUJIFILM Biotechnologies in Holly Springs, NC, is hosting an invite-only Manufacturing Associate hiring event on October 24. Selected candidates will be screened in advance and asked to provide interview availability.

Open roles range from Manufacturing Associate II to V. You will support manufacturing operations in a regulated environment, follow SOPs, operate equipment, and help maintain cGMP/5S compliance while collaborating with Quality, Engineering and Planning.

Qualifications

• Experience in manufacturing or related field; level commensurate with role (II-V).
• Familiarity with GMP/cGMP or regulated production environments preferred
• Ability to follow SOPs, document accurately, and meet throughput targets
• Strong attention to detail, teamwork, and communication skills
• Willingness to work [shift/rotating/weekends], as needed
• Physical requirements: ability to stand for extended periods and lift up to [X] lbs

Responsibilities

• Support manufacturing operations in a regulated environment to meet safety, quality, and production goals
• Execute standard operating procedures (SOPs) and batch records accurately
• Operate, monitor, and troubleshoot production equipment; perform in-process checks
• Maintain cGMP/5S compliance, documentation, and area readiness
• Collaborate with cross-functional teams (Quality, Engineering, Planning)
• Contribute to continuous improvement, root cause analysis, and safety initiatives

Skills

Attention to detail

Teamwork

Communication skills

Ability to follow SOPs

Job description

FUJIFILM Biotechnologies in Holly Springs, NC, is hosting an invite-only Manufacturing Associate hiring event on October 24. Selected candidates will be screened in advance and asked to provide interview availability.

Open roles range from Manufacturing Associate II to V. You will support manufacturing operations in a regulated environment, follow SOPs, operate equipment, and help maintain cGMP/5S compliance while collaborating with Quality, Engineering and Planning.