Manufacturing Process Associate

Katalyst CRO; Durham (NC); On-site; USD 25,000 - 30,000; Full time

Job summary

Katalyst CRO is seeking a Manufacturing Process Associate in Durham, NC. The role supports daily production in a GMP-regulated environment, operating equipment, documenting batches, and ensuring quality.

Responsibilities include equipment setup, changeovers, inspections, and maintaining material inventory, while upholding GMP and safety standards. Collaboration and meticulous work are essential to success.

Qualifications

• GMP and manufacturing practices knowledge required.
• Ability to follow written procedures precisely.
• Proficient with basic computer applications.
• Strong communication and teamwork skills.
• Attention to detail is essential.

Responsibilities

• Operate manufacturing equipment according to SOPs and work instructions.
• Monitor production processes and complete batch documentation.
• Perform equipment setup, cleaning, and changeovers.
• Conduct visual inspections and report quality concerns.
• Maintain inventory of production materials.
• Follow GMP, safety, and quality procedures.
• Support continuous improvement initiatives.
• Perform other assigned duties.

Skills

GMP Knowledge

Follow SOPs

Basic computer skills

Good communication

Attention to detail

Teamwork

Education

High School Diploma or Associate Degree

Job description

Job Title: Manufacturing Process Associate

Location: Durham, NC 27703

Duration: 12 Months (Extension Possible)

Shift: Day Shift - Monday to Friday, 7:00 AM - 3:30 PM

Summary

The Manufacturing Process Associate supports daily production activities in a GMP-regulated manufacturing environment. This position is responsible for operating equipment, maintaining documentation, performing inspections, and ensuring products meet quality standards.

Key Responsibilities

• Operate manufacturing equipment according to SOPs and work instructions.
• Monitor production processes and complete batch documentation.
• Perform equipment setup, cleaning, and changeovers.
• Conduct visual inspections and report quality concerns.
• Maintain inventory of production materials.
• Follow GMP, safety, and quality procedures.
• Support continuous improvement initiatives.
• Perform other assigned duties.

Education

• High School Diploma or Associate Degree preferred.

Mandatory Skills

• Knowledge of GMP and manufacturing practices.
• Ability to follow written procedures.
• Basic computer skills.
• Good communication and teamwork.
• Strong attention to detail.

Experience Required

• 1-3 years of manufacturing or production experience preferred.
• Medical device, pharmaceutical, or food manufacturing experience is a plus.