Downstream Processing Operator

Danimer Scientific; Winchester (KY); On-site; USD 40,000 - 60,000; Full time

Benefits offered by this job

401(k)

Health insurance

Training & development

Job summary

Danimer Scientific in Winchester, KY is seeking a Downstream Processing (DSP) Operator to handle advanced materials production in a cGMP environment. The role requires strong attention to detail and teamwork, ensuring all processes follow strict quality standards.

Ideal candidates will have at least 2 years of manufacturing experience and a high school diploma. Benefits include 401(k), health insurance, and ongoing training opportunities for career development.

Qualifications

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

Responsibilities

• Operate and monitor downstream processing equipment and utilities.
• Accurately complete batch records, logbooks, and production documentation.
• Troubleshoot process or equipment deviations and initiate corrective actions.

Skills

Attention to detail

Problem-solving skills

Teamwork

Automated systems proficiency

Education

High school diploma or GED

Associate degree in applied process technologies

Tools

Microsoft Suite

Job description

Downstream Processing (DSP) Operator

Location: Winchester, KY

Job Summary

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.

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 operatorsServe as a safety leader—stop production when a quality or safety concern is identified

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 on a 2‑2‑3 pattern (day or night availability required)
• 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

Benefits

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

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.