Automation Engineer

About the role

The successful candidate will play a key role in ensuring that all automated manufacturing processes align with the validation strategies and quality procedures. They will also assist in developing vision and programming standards and conduct source code reviews for automated equipment.

Responsibilities

• Ensure alignment of automated manufacturing processes with validation strategies and quality procedures.
• Aid in the development of vision and programming standards and perform source code reviews for automated equipment.
• Provide guidance to suppliers on new equipment builds and analyze production equipment performance.
• Develop plans to increase yield from underperforming inspections.
• Manage projects that may compete for your time while keeping accurate records of work.
• Demonstrate a solid understanding of the importance of quality and documentation.
• Work with Allen Bradley PLC’s, Cognex Vision systems, and Fanuc Robots.

Requirements

• 2+ years of experience in Automated Manufacturing.
• Validation experience, process and equipment qualification (IQ, OQ, PQ), and Test Methods are a plus.
• Compose professional documentation (write protocols, work instructions, engineering studies, etc.).
• Manage time and projects effectively while setting and meeting ambitious schedules.
• Knowledgeable on regulatory requirements, FDA 21 CFR 820/GMP Medical Device Regulations.
• Working knowledge of Minitab.
• Knowledge of statistical techniques and sampling for process validation and process monitoring is desired.

Qualifications

• Mastery of at least one of Allen Bradley PLC’s, Cognex Vision systems, or Fanuc Robots is preferred.
• Basic background requirements include:
• 2+ years of experience in Automated Manufacturing.
• Validation experience, process and equipment qualification (IQ, OQ, PQ), and Test Methods are a plus.
• Compose professional documentation (write protocols, work instructions, engineering studies, etc.).
• Manage time and projects effectively while setting and meeting ambitious schedules.
• Knowledgeable on regulatory requirements, FDA 21 CFR 820/GMP Medical Device Regulations.
• Working knowledge of Minitab.
• Knowledge of statistical techniques and sampling for process validation and process monitoring is desired.

Skills

• Strong project management skills.
• Ability to manage multiple tasks simultaneously.
• Excellent communication and documentation skills.
• Understanding of regulatory requirements and GMP guidelines.
• Experience with Allen Bradley PLC’s, Cognex Vision systems, and Fanuc Robots.

Benefits

• 3 weeks of Paid Time Off (PTO) starting your 1st year.
• 10 paid holidays.
• Potential for annual profit sharing bonus based on company performance.
• Major health, dental, vision, and complementary insurances offered starting day 1.
• A 50% match on your first 6% of 401k contribution with opportunity for an employer contribution annually.

Pay

Details on pay are not specified in the job posting.

Schedule

Details on schedule are not specified in the job posting.