Controls Engineer I

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Job description

Controls Engineer I Canton, MA

Job Req code: 929

Category: Production

Organogenesis corporate headquarters is located in Canton, Massachusetts, including manufacturing, R&D, customer service, reimbursement and other corporate teams supporting our full range of products. We have unique opportunities and are always looking for exceptional talent. Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing.

The Controls Engineer I role is part of the Process Engineering department, which supports all aspects of the manufacturing process from supply chain to shipment. The team assists in product design, development, and are responsible for developing and testing solutions to solve a wide variety of technical problems.

The Controls Engineer I will serve as a Subject Matter Expert (SME) for facility expansion and other engineering tasks as required. The individual will provide technical expertise regarding large process equipment, and other PLC/HMI controlled equipment. As a core team member, the Controls Engineer I will oversee/monitor the work of others, including contractors. The position will use process knowledge to successfully plan, design, and startup a new manufacturing site. The role will participate in projects to improve product yield increase capacity and/or reduce overall production cost, and will support all manufacturing systems, current and new.

A successful candidate will be an independent self-starter who can work with minimal direction and who takes ownership of a job from concept through manufacturing/implementation. The successful candidate will be highly motivated and a creative individual.

Key Responsibilities

• Bachelor's Degree in Engineering or equivalent with a minimum of 2 to 4 years' relevant work experience
• Demonstrated ability to develop and implement control system integrating PLC/HMI components.
Experience with Allen Bradley PLC control systems
• Experience working in a GMP environment/medical device industry.
• Ability to read, write functional requirement specifications, follow verbal instructions, interpret technical procedures, and technical writing skills beneficial.
• Ability to develop and execute test plans to validate systems.
• Experience with large process equipment (autoclaves, glass washers, ovens, centrifuges, etc.)
• Ability to read, write and comprehend English.
• Good computing skills including Microsoft office.
• Work well with others and have communication and interpersonal skills.
• Ability to solve practical problems both individually and in a team environment.
• Work independently with minimal supervision.

RequirementsOther Skills/Abilities

• Experience using AutoCAD and/or Solidworks
• Experience in medical device design and application of test standards.
• Experience working in a hands-on environment.
• Familiar with validation methods (IQ/OQ/PQ)
• Knowledge of GMP, GAMP guidelines, IEEE specifications, ISA specifications, ASTM specifications and batch process control in the life science industry.

Preferred Education and Experience

Bachelor's Degree in Engineering or equivalent with a minimum of 2 to 4 years' relevant work experience