DSM Manufacturing Associate III — 24/7 Biotech Ops Lead

FUJIFILM Biotechnologies

Holly Springs (NC)

Sur place

USD 52 000 - 68 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Shift differentials
Health coverage
Retirement plan
Paid time off
Training & certs
Career growth
Inclusive culture
PPE provided

Résumé du poste

Fujifilm Biotechnologies in Holly Springs, North Carolina, operates a 24/7 bulk drug substance manufacturing facility. As a Manufacturing Associate 3, you will lead processing steps, help bring new capacity online, and ensure safe, compliant production on time.

You will perform in-process testing, execute validation protocols, and maintain training to perform activities. The role requires weekend shifts and possible nights, with 0–25% travel during project phases, fostering growth in a

Qualifications

  • High school/GED with 4 years' manufacturing experience.
  • Bachelor's degree in Life Sciences or Engineering.
  • Associate's degree with 2 years in cGMP manufacturing.
  • Equivalent military training or experience.
  • Experience in at least one unit operation (DPFG Filler or Cell Culture - Seed Train).

Responsabilités

  • Lead and document manufacturing processing steps.
  • Perform in-process testing (pH, conductivity, visual inspection).
  • Execute validation protocols per cGMP SOPs.
  • Maintain required training to perform activities.
  • Manage materials and cycle counts; support 24/7 operation.
  • Support readiness activities for bulk drug substance manufacturing.
  • Travel up to 0-25% during project phase.

Connaissances

Troubleshooting
Communication
Teamwork
cGMP
Equipment knowledge

Formation

High school/GED
Associate's degree
Bachelor's degree Life Sciences/Engineering
Associate's degree + 2 years
Equivalent military training

Outils

BioWorks / Capstone cGMP coursework

Description du poste

Fujifilm Biotechnologies in Holly Springs, North Carolina, operates a 24/7 bulk drug substance manufacturing facility. As a Manufacturing Associate 3, you will lead processing steps, help bring new capacity online, and ensure safe, compliant production on time.

You will perform in-process testing, execute validation protocols, and maintain training to perform activities. The role requires weekend shifts and possible nights, with 0–25% travel during project phases, fostering growth in a

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