Equipment Engineer II – Manufacturing & Validation

Regenity Biosciences; Allendale (NJ); On-site; USD 85,000 - 105,000; Full time

Benefits offered by this job

Company performance bonus eligibility

401(k) plan with company contribution

Paid time off and paid holidays

Medical, prescription, dental, and vis

Company-paid life and AD&D insurance

Wellness Program and EAP

Tuition Reimbursement

Job summary

Regenity Biocences, Inc. seeks an Equipment Engineer II to support manufacturing operations and validation activities, driving safety, productivity, yields, and process reliability.

You will engage in commissioning, equipment qualification, SOPs, and vendor transfers, contributing to cost reductions and reliability improvements. The role requires a mechanical engineering degree and 6–10 years of industry experience within regulated environments such as medical devices or ISO 9000+.

Qualifications

• Strong technical writing and review skills.
• Excellent verbal and written communication abilities.
• Ability to manage change and grasp new concepts quickly.

Responsibilities

• Perform commissioning and qualification of new equipment.
• Prepare and review equipment qualification reports.
• Write or revise standard operating procedures.
• Troubleshoot equipment performance issues and determine root causes.
• Transfer new equipment into manufacturing with R&D and others.

Skills

Verbal communication

Written communication

Troubleshooting

Self-starter

Education

Bachelor's degree in Mechanical Engineering or equivalent

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Regenity Biocences, Inc. seeks an Equipment Engineer II to support manufacturing operations and validation activities, driving safety, productivity, yields, and process reliability.

You will engage in commissioning, equipment qualification, SOPs, and vendor transfers, contributing to cost reductions and reliability improvements. The role requires a mechanical engineering degree and 6–10 years of industry experience within regulated environments such as medical devices or ISO 9000+.