Pharma Manufacturing Operator I – Growth & Training

NCBiotech

Clayton (NC)

On-site

USD 25,000 - 39,000

Full time

5 days ago
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Benefits offered by this job

Health Insurance
Dental Insurance
Vision Insurance
14 paid holidays
401K with company match

Job summary

Novo Nordisk in Clayton, NC seeks a position to operate utility and RMS process equipment to support API-US production. Responsibilities include operation of equipment within the department, receiving materials, training, and supporting quality and financial goals.

Join a global network of manufacturing professionals. The role emphasizes safety, adherence to cGMP, and collaboration with internal and external stakeholders; EHS compliance is essential.

Qualifications

  • High school diploma or GED required (degree preferred)
  • Bachelor’s Degree in a relevant field preferred
  • BioWork certification or equivalent a plus
  • Minimum of 6 months related experience in regulated industry required
  • Familiarity with FDA, cGMP, OSHA in a regulated environment
  • Ability to read and review equipment documents and operate electronic batch records

Responsibilities

  • Operate equipment and processes per SOPs for nGMP and GMP systems
  • Identify and document anomalies to minimize downtime and ensure safety
  • Maintain standards and procedures for automated and manual systems
  • Support control systems (BMS, PCS, Life Safety) and routine maintenance
  • Execute raw material movement and offload into process systems
  • Conduct site rounds and equipment inspections for efficiency and compliance
  • Follow safety and environmental requirements and perform housekeeping as needed

Skills

Problem solving
Safety mindset
Quality awareness
Documentation skills

Education

Bachelor’s Degree in a relevant field
BioWork certification

Tools

DeltaV
Syncade
Electronic batch records

Job description

Novo Nordisk in Clayton, NC seeks a position to operate utility and RMS process equipment to support API-US production. Responsibilities include operation of equipment within the department, receiving materials, training, and supporting quality and financial goals.

Join a global network of manufacturing professionals. The role emphasizes safety, adherence to cGMP, and collaboration with internal and external stakeholders; EHS compliance is essential.

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