MSAT Process Engineer — GMP Biopharma Process Improvement

Ring Inc

Princeton (NJ)

On-site

USD 80,000 - 100,000

Full time

14 days+
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Benefits offered by this job

Annual bonus
Medical, dental, and vision coverage
PTO
401(k) plan
Life and AD&D insurance
Parental leave
Pre-IPO equity

Job summary

Ring Inc is seeking a MSAT Process Engineer to improve the efficiency and safety of drug product manufacturing. You will manage lifecycle activities for clinical and commercial products, monitor processes, and drive improvements with validation and change control execution.

Responsibilities include monitoring, reporting, investigations, CAPA, and supporting validation protocols, change controls, and testing within lifecycle management.

Qualifications

  • B.S. in Engineering or similar field.
  • 3+ years in manufacturing processes and equipment.
  • Experience in regulated GMP manufacturing operations.
  • Biotechnology and cell therapy experience preferred.
  • Strong communication and problem solving skills.
  • Flexibility to work outside standard hours when needed.

Responsibilities

  • Monitors existing products and processes.
  • Generates metrics and reports for process monitoring and continuous verification.
  • Supports process improvements and changes including electronic batch records.
  • Investigates process events and implements CAPA.
  • Provides troubleshooting for manufacturing events, equipment, and materials.
  • Performs root cause analysis and determines corrective actions.
  • Owns change controls, protocols, reports, and lifecycle activities.
  • Writes and validates testing protocols in line with lifecycle management.

Skills

Strong communication
Problem solving
Shift flexibility
GMP experience

Education

B.S. in Engineering or related field

Job description

Ring Inc is seeking a MSAT Process Engineer to improve the efficiency and safety of drug product manufacturing. You will manage lifecycle activities for clinical and commercial products, monitor processes, and drive improvements with validation and change control execution.

Responsibilities include monitoring, reporting, investigations, CAPA, and supporting validation protocols, change controls, and testing within lifecycle management.

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