Downstream Processing Operator

Danimer Scientific, Inc

Winchester (KY)

On-site

USD 45,000 - 60,000

Full time

14 days+

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Benefits offered by this job

Health insurance
401(k) matching
Bonus based on performance
Training & development
Wellness resources

Job summary

Danimer Scientific, Inc in Winchester, KY seeks a Downstream Processing Operator to produce advanced materials in a cGMP manufacturing setup. You will operate and monitor equipment, perform quality checks, and ensure compliance with safety standards.

This hands-on role requires a high school diploma, at least 2 years of manufacturing experience, and an ability to work in a dynamic environment. The position offers full-time 12-hour shifts with great pay and benefits, including health insurance and 401(k) options.

Qualifications

  • Minimum of 2 years of experience in a manufacturing or industrial environment.
  • Comfortable working with automated systems and manual equipment.
  • Strong attention to detail and commitment to documentation accuracy.

Responsibilities

  • Operate and monitor downstream processing equipment and utilities.
  • Submit production documentation in compliance with cGMP standards.
  • Train and support new or developing operators.

Skills

Attention to detail
Problem-solving skills
Team collaboration
Mechanical inclination

Education

High school diploma or GED
Associate degree in applied process technologies

Tools

Microsoft Suite

Job description

Benefits
  • 401(k)
  • 401(k) matching
  • Bonus based on performance
  • Dental insurance
  • Health insurance
  • Training & development
  • Vision insurance
  • Wellness resources
Location & Schedule

Winchester, KY | Biodegradable Plastics

Schedule: 12 Hour Shifts on a 2-2-3 pattern (Day or Night Availability Required)

Employment Type: Non-exempt | Full-time

Job Overview

At Danimer Scientific, we’re building the future of sustainable materials—and that takes skilled operators who care about quality, safety, and doing things the right way. As a Downstream Processing (DSP) Operator, you’ll play a hands‑on role in producing advanced materials in a cGMP manufacturing environment while working with a collaborative, safety-focused team.

What You’ll Do

Under the guidance of a Team Leader and Manufacturing Management, the DSP Operator is responsible for executing day‑to‑day production activities in the Downstream Processing area. This role is hands‑on, detail-oriented, and critical to maintaining product quality and process reliability.

Key Responsibilities
  • Operate and monitor downstream processing equipment and utilities
  • Start/stop pumps, open/close manual valves, collect samples, and respond to process alarms
  • Monitor process conditions and adjust parameters to maintain stability
  • Accurately complete batch records, logbooks, and production documentation in compliance with cGMP standards
  • Review production documentation for accuracy, completeness, and quality compliance
  • Add chemicals and process additives based on calculations and procedures
  • Troubleshoot process or equipment deviations and initiate corrective actions
  • Communicate production metrics, issues, and shift handoffs clearly
  • Maintain clean, organized, and audit-ready work areas per GMP standards
  • Participate in continuous improvement initiatives related to safety, quality, and efficiency
  • Train and support new or developing operators
  • Serve as a safety leader—stop production when a quality or safety concern is identified
What We’re Looking For
Required Qualifications
  • High school diploma or GED
  • Minimum of 2 years of experience in a manufacturing or industrial environment
  • Ability to work independently and as part of a team
  • Strong attention to detail and commitment to documentation accuracy
  • Mechanically inclined with strong problem‑solving skills
  • Comfortable working with automated systems and manual equipment
  • Proficient with basic computer systems (Microsoft Suite)
Preferred Qualifications
  • Associate degree in applied process technologies or related field
  • Prior experience in biotech, chemical, or cGMP manufacturing
  • Working knowledge of GMP, safety protocols, and quality systems
Work Schedule
  • Full-time, 12-hour shifts
  • Days or nights, including weekends, holidays, and overtime as required
Physical & Work Environment Requirements
  • Ability to stand, walk, bend, stoop, and perform repetitive tasks for extended periods
  • Ability to lift up to 50 lbs occasionally and climb ladders/stairs
  • Work in hot, cold, loud, and industrial manufacturing environments
  • Use of PPE including hearing protection in designated areas
  • Exposure to moving mechanical parts, vibration, fumes, and airborne particles
Why Danimer?

Mission-driven work (bye, plastic pollution)

Growth opportunity

Great pay + benefits

Team-first culture

Equal Opportunity Employer

Danimer Scientific provides equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, national origin, age, disability, genetics, or any other status protected by law. We comply with all federal, state, and local laws governing nondiscrimination in every location where we operate.

We strictly prohibit any form of workplace harassment or discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, or any other protected status.

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