GMP Manufacturing Operator - Batch Records & Automation

Katalyst CRO

Durham (NC)

On-site

USD 65,000 - 90,000

Full time

5 days ago
Be an early applicant
Application generator

Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.

Get past ATS filters

Job summary

Katalyst CRO in Durham, NC seeks a Manufacturing Operations Specialist to support pharmaceutical manufacturing—operating production equipment, executing batch records, and maintaining GMP compliance for safe, efficient operations.

Responsibilities include equipment changeovers, electronic batch documentation, deviation support, and participation in shift handoffs and continuous improvement initiatives. A relevant degree is required.

Qualifications

  • Must have pharmaceutical/biotech manufacturing experience.
  • Experience with GMP facilities or regulated environments.
  • Familiarity with electronic batch records and manufacturing systems.
  • Experience operating automated manufacturing equipment.

Responsibilities

  • Operate manufacturing equipment following SOPs and batch records.
  • Execute manufacturing processes in GMP-compliant manner.
  • Complete electronic batch documentation accurately.
  • Perform equipment cleaning and changeovers.
  • Monitor production processes and identify abnormalities.
  • Support deviation investigations and corrective actions.
  • Maintain inventory of manufacturing supplies.
  • Participate in shift handoffs and production meetings.
  • Follow safety and environmental procedures.
  • Support continuous process improvement initiatives.

Skills

Operate equipment
GMP compliance
Electronic batch records
Batch documentation
Process improvement
Safety procedures

Education

Associate or Bachelor's in biology/ Biotechnology/ Chemistry

Tools

Automated manufacturing equipment
Manufacturing systems

Job description

Katalyst CRO in Durham, NC seeks a Manufacturing Operations Specialist to support pharmaceutical manufacturing—operating production equipment, executing batch records, and maintaining GMP compliance for safe, efficient operations.

Responsibilities include equipment changeovers, electronic batch documentation, deviation support, and participation in shift handoffs and continuous improvement initiatives. A relevant degree is required.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Day Shift GMP Manufacturing Process Associate
Day Shift GMP Manufacturing Process Associate

Katalyst CRO • Durham (NC)

On-site
USD 25,000 - 30,000
OSD Manufacturing Technician - GMP & Equipment Specialist
OSD Manufacturing Technician - GMP & Equipment Specialist

Katalyst CRO • Wilson (NC)

On-site
USD 42,000 - 62,000
Biopharma Process Technician I: GMP & Equipment Ops
Biopharma Process Technician I: GMP & Equipment Ops

MedPharm Ltd • Durham (NC)

On-site
USD 42,000 - 64,000
GMP Packaging Operator I — Precise, Safe Manufacturing
GMP Packaging Operator I — Precise, Safe Manufacturing

Katalyst CRO • Tampa (FL)

On-site
USD 32,000 - 46,000
Aseptic cGMP Manufacturing Operator I
Aseptic cGMP Manufacturing Operator I

Katalyst CRO • Portsmouth (NH)

On-site
USD 42,000 - 60,000
Production Operator I - GMP/Quality Focus
Production Operator I - GMP/Quality Focus

Katalyst CRO • Sparks Corner (MD)

On-site
USD 42,000 - 56,000
GMP Manufacturing Operator - Pharma Production & Quality
GMP Manufacturing Operator - Pharma Production & Quality

Actalent • New Jersey

On-site
USD 42,000 - 62,000
GMP Manufacturing Technician III: Process & Quality
GMP Manufacturing Technician III: Process & Quality

Katalyst CRO • Sparks Corner (MD)

On-site
USD 60,000 - 90,000
Biopharma Process Technician: cGMP Ops & Validation
Biopharma Process Technician: cGMP Ops & Validation

MedPharm • Durham (NC)

On-site
USD 40,000 - 60,000
Manufacturing Operations Specialist
Manufacturing Operations Specialist

Katalyst CRO • Durham (NC)

On-site
USD 65,000 - 90,000