Senior Aseptic Production Operator – Parenteral Manufacturing

Indivior PLC

Raleigh (NC)

Presencial

USD 41 000 - 55 000

Tempo integral

Há 6 dias
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Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

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Vantagens oferecidas por esta oferta de emprego

Starting salary
PTO
Bonus program
Health, dental, vision
HSA options
Tuition reimbursement

Resumo da oferta

Indivior PLC is seeking an Operator III, Aseptic Production to operate and monitor aseptic processing equipment in a regulated setting. The role emphasizes strict adherence to cGMPs, batch documentation, and cleanroom practices.

You will interact with Quality Assurance, Maintenance and Engineering staff to ensure production lines run smoothly while maintaining safety and data integrity. A minimum of five years in a regulated environment is required.

Qualificações

  • High School Diploma required.
  • Minimum five (5) years’ experience in a regulated environment.
  • Gowning experience in a classified area is required.
  • Understanding of aseptic techniques required.
  • Knowledge of cGMPs.
  • Basic math and science skills and the ability to use a computer.
  • Strong communication skills, both verbal and written.
  • Attention to detail and accuracy in documentation.

Responsabilidades

  • Operate processing and test equipment in aseptic areas per SOPs.
  • Monitor operations and review data to ensure requirements are met.
  • Document batch records, logbooks and related production data.
  • Maintain clean, safe work areas and proper equipment sanitization.
  • Communicate with Production, Quality, Maintenance and Engineering teams.

Conhecimentos

Aseptic techniques
Communication
Mechanical aptitude
Documentation

Formação académica

High School Diploma

Ferramentas

Filling equipment
Lyophilizer
Steam sterilizers

Descrição da oferta de emprego

Indivior PLC is seeking an Operator III, Aseptic Production to operate and monitor aseptic processing equipment in a regulated setting. The role emphasizes strict adherence to cGMPs, batch documentation, and cleanroom practices.

You will interact with Quality Assurance, Maintenance and Engineering staff to ensure production lines run smoothly while maintaining safety and data integrity. A minimum of five years in a regulated environment is required.

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