Night Manufacturing Lead — 12h Shifts, 15% Differential

BioSpace

West Greenwich (RI)

On-site

USD 70,000 - 100,000

Full time

20 hours ago
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Benefits offered by this job

Shift differential
Sunday premium pay

Job summary

Amgen in the United States is seeking a Senior Associate Manufacturing - Nights to lead production activities in the Inoc/Seeds area. You will execute operations under SOPs, participate in validation, draft and revise documents, and support a culture of safety and continuous improvement.

The role emphasizes quality, compliance, and collaboration with Quality, Engineering, Process Development, and Regulatory teams.

Qualifications

  • High school diploma / GED with 4 years of Manufacturing or Operations experience.
  • Associates degree with 2 years of Manufacturing or Operations experience.
  • Bachelors degree with 6 months of Manufacturing or Operations experience OR Masters degree.
  • Knowledge of GMP/CFR regulations and basic statistical methods.
  • Ability to interpret and write SOPs, MP documents and technical reports.

Responsibilities

  • Lead manufacturing operations on the production floor.
  • Ensure safety and compliance procedures are followed at all times.
  • Support equipment qualification, validation, and issue resolution.
  • Provide troubleshooting and technical support for equipment, automation, and processes.
  • Write, revise, and own SOPs and manufacturing documentation.
  • Collaborate with Quality, Engineering, and Regulatory staff on manufacturing events.

Skills

Manufacturing experience
Troubleshooting
GMP knowledge
Technical writing
Cross-functional collaboration

Education

Bachelor's degree in manufacturing or related field
Associate's degree
Master's degree

Tools

Delta V
R&D/Development systems (RDs)
LIMS
Process equipment

Job description

Amgen in the United States is seeking a Senior Associate Manufacturing - Nights to lead production activities in the Inoc/Seeds area. You will execute operations under SOPs, participate in validation, draft and revise documents, and support a culture of safety and continuous improvement.

The role emphasizes quality, compliance, and collaboration with Quality, Engineering, Process Development, and Regulatory teams.

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