Sterile Manufacturing Associate

Nivagenpharmaceuticals

Sacramento, CA, United States
$28 - $32 ph; annual bonus eligibility; medical, d...
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Aseptic manufacturing operations
Cgmp compliance
Cleanroom environments
** Nivagen Pharmaceuticals is seeking a Sterile Manufacturing Associate to execute aseptic manufacturing operations in compliance with regulatory standards at their Sacramento, CA facility. The ideal candidate should have experience in sterile environments and a strong attention to detail, with a commitment to following precise protocols. **

Job Summary

  • The Manufacturing Associate is responsible for executing aseptic and cleanroom manufacturing operations in compliance with cGMP, regulatory standards, and internal SOPs.
  • Perform aseptic manufacturing operations in Grade A, B, C, and D cleanroom environments, including formulation, filtration, filling, and visual inspection.
  • Nivagen Pharmaceuticals affords equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors.

Matching Summary

Match Score: 75

** Nivagen Pharmaceuticals is seeking a Sterile Manufacturing Associate to execute aseptic manufacturing operations in compliance with regulatory standards at their Sacramento, CA facility. The ideal candidate should have experience in sterile environments and a strong attention to detail, with a commitment to following precise protocols. **

Salary

$28 - $32 per hour; Annual Bonus eligibility; Medical, Dental, and Vision coverage, PTO plan, 401K plan

Skills & Requirements

Must-have

  • Aseptic manufacturing operations
  • cGMP compliance
  • Cleanroom environments
  • Gowning and aseptic techniques
  • Batch production records

Nice-to-have

  • Continuous improvement initiatives
  • Collaboration with Quality and Validation

Key Requirements

  • High School diploma or GED
  • Experience in aseptic or sterile pharmaceutical manufacturing
  • Experience in cGMP-regulated environments
  • Ability to stand for extended periods
  • Ability to lift up to 50 pounds
  • Legally authorized to be employed in the United States

Work Rights

Legally authorized to be employed in the United States

Tailored Resume

Cover Letter