Manufacturing Engineer

Rapid Micro Biosystems • Lowell, MA

282d • Onsite

About The Position

Winning the race to bring new healthcare products safely to a waiting world drives Rapid Micro Biosystems (RMB) to combine today's innovative technologies as never before. Your career at RMB puts you at the center of diverse global teams that span robotics, AI, Machine Learning, imaging, microbiology, and more, re-shaping how urgently needed pharmaceuticals are made, tested, and released for decades to come. The sky's the limit. Careers at RMB are fast-moving, with the high growth you'd expect from a world leader in microbiology automation. Advancement at RMB affords an opportunity to achieve your personal goals and develop your passions, in an inclusive environment where every employee has the resources and opportunities to hone their skills. You'll do more, learn more, and have the ability to make a profound impact on our business. GENERAL DESCRIPTION: Are you a passionate engineer looking to apply your skillset in bringing capable and scalable processes into a GMP environment? Rapid Micro Biosystems is looking for a New Product Manufacturing Engineer I/II who will be responsible for the design transfer of new products to our manufacturing facility. This position is vital to the Operations organization to ensure that highly capable processes will be implemented for our new products. The successful candidates excel at problem-solving skills and can manage complex projects within a cross-functional team.

Requirements

• Bachelor's or Master's degree in Engineering is required.
• 3+ years of manufacturing/process engineering experience required.
• 2+ years of experience bringing new designs/processes into a GMP environment.
• Ability to work within a highly collaborative team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Strong verbal and written communications with the ability to effectively communicate at multiple levels across different shifts in the organization.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to maintain regular and predictable attendance.
• Understand engineering principles, theories, concepts, practices, and techniques.

Nice To Haves

• Equipment and process validation experience in medical device or other regulated industry.
• Work with vendor/suppliers to design, procure, and fabricate equipment tooling and fixtures.
• Utilize statistical tools like Gage R&R, Cp, Cpk, and Statistical Process Controls.
• Understand manufacturing and problem-solving concepts like Value Stream mapping, 6S, and A3 to improve quality, labor efficiency, throughput, and ensuring the root cause of problem is identified and quickly resolved.
• Experience with automated or robotic equipment and systems.

Responsibilities

• Participate in New Product Development teams and represent Operations.
• Participate in the development of robust, scalable, and high-quality solutions for new products in the cGMP environment.
• Lead specific deliverables within the Design Transfer process and ensure adherence to the project timeline.
• Lead the root-case and corrective action response and countermeasure implementation for production issues, product defects, customer complaints, and any other technical challenge that may arise, for new products.
• Identify and implement opportunities to improve existing processes, equipment, systems, and infrastructure by leveraging and setting industry best practices.
• Generate and modify manufacturing process documentation.
• Train and/or provide work instructions to operators/technicians.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree