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Engineer II
TMRW New York, NY
$94k-112k (estimate)
Full Time 4 Months Ago
Save

TMRW is Hiring an Engineer II Near New York, NY

Engineer II

THE RIGHT CANDIDATE

We’re looking for a creative, collaborative, resourceful, thoughtful, smart, entrepreneurial team member who has a passion for our mission and shares our values. The right candidate will thrive in a fast-paced environment, celebrate winning as a team and be resourceful in finding, creating, and implementing solutions. They will balance moving swiftly and thoroughly while ensuring that they are contributing to our collaborative team environment. They will care equally about achieving excellent results and ensuring everyone involved feels a valued part of the team. This person will be a key ambassador for our company.

The successful candidate is a quick learner who will seek first to understand, work with the current team to get up to speed, utilize and synthesize work that has already been done to get up to speed quickly on the business. They must be comfortable in a start-up environment and thrive on finding creative solutions. There is no playbook outside of the mission we share and the values we embrace. 

ROLE

As an Engineer II within TMRW Life Sciences, you will play a crucial role in the design and support of our cryogenic storage medical device product development team. Operating in a dynamic and cross-functional environment, you will leverage your engineering expertise to enhance TMRW's product portfolio, ensuring its excellence in usability, environmental impact, and safety. This role is based in the New York City office.

Key Responsibilities:

  • Collaborate within a cross-functional environment to contribute to the development and support of TMRW Life Sciences products.
  • Utilize your experience, knowledge, and skills to design innovative solutions that enhance and expand TMRW's product portfolio.
  • Assess and test the usability, impact, and safety of designs, providing valuable insights for continuous improvement.
  • Employ computer-aided design (CAD) and computer-aided engineering (CAE) software to create detailed prototypes and design iterations.
  • Generate design control documents, including product requirements, drawings, label specifications, manufacturing specifications, and risk documents such as Design and Process FMEA.
  • Collect and analyze data from tests conducted on prototypes, making data-driven decisions for design modifications and improvements.
  • Manage the development process, overseeing project progress and costs, and ensuring effective communication within project teams.
  • Evaluate proofs and prototypes, executing First Article Inspections (FAIs) to ensure design integrity and compliance.
  • Conduct product testing and design verification testing to ensure product performance meets established standards.
  • Participates in cross functional projects and initiatives.
  • Other duties as assigned.

You must be an enterprising self-starter, comfortable with ambiguity, and focused on flawless execution. You will win by turning ideas into action, strategy into tangible execution that will create value for TMRW and our customers. You will work closely with our Field Service, TMRW Operations Center (TOC), Engineering, Quality & Supply Chain teams. 

WHAT YOU'LL NEED TO SUCCEED

  • Bachelor’s degree in engineering or related field; Master's degree is a plus.
  • 5 years’ experience in product development for complex medical device systems in a regulated environment(ISO 13485)is preferred.
  • 5 years’ experience with manufacturing processes including: injection molding, vacuum forming, thermoforming, 3D Printing, PCBA manufacturing and firmware, electromechanical devices, CNC Machining.
  • Proficiency in computer-aided design (CAD) and computer-aided engineering (CAE) software.
  • Strong analytical and problem-solving skills with attention to detail.
  • Excellent communication and collaboration abilities within a cross-functional team.
  • Demonstrated experience with design control processes and documentation, selection of materials and manufacturing processes.
  • Ability to manage multiple tasks and projects simultaneously.
  • Demonstrated ability in technical writing, specifically for controlled process documentation in a regulated industry
  • Exceptional technical presentation and communication skills
  • You are a curious collaborator and strong team player

ABOUT US

TMRW Life Science’s mission to safeguard life’s most precious cells. We design technology that provides safety and transparency to modernize and transform IVF. Our platform revolutionizes the management, identification, tracking, storage and care of frozen eggs and embryos used in IVF. Developed in partnership with leading fertility doctors and embryologists, TMRW’s technology will play a central role in the births of tens of millions of people in the coming years by setting a new standard of care in the IVF industry.

Our team includes many pioneering leaders in clinical medicine, reproductive biology, embryology, and cryogenic biobanking who have synthesized their collective knowledge, vision, and experience in the development of the TMRW platform. We’re committed to bringing together a diverse, cross-disciplinary team to achieve our mission — and we’re always looking for more innovators to join us in creating a better tomorrow.

At TMRW, we know that cultivating diversity and fostering an inclusive work environment is critical to our impact and success. We create an environment where no individual is advantaged or disadvantaged because of their background. We offer equal opportunity employment regardless of race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, marital status, or protected veteran status.

With a commitment to maintaining a bias-free environment where harassment is prohibited, we respect cultural diversity and comply with the laws of the places we operate. We expect our business partners, suppliers, clients, and team members to uphold these commitments.

We look for people who share our values. They are our promise to each other and the guideposts for our day-to-day work. 

Our TMRW values:

Integrity is our non-negotiable.

Excellence is our standard.

Collaboration is how we win.

Trailblazing is our spirit.

Service is our passion.

Care is at the heart of everything we do.

EEO Statement

Equal Opportunity Employer

TMRW Life Sciences, Inc. is proud to be an equal opportunity employer and is committed to maintaining a diverse and including work environment. All qualified applicants will receive considerations for employment without regard to race, color, religion, sex, age, disability, marital status, familial status, sexual orientation, pregnancy, genetic information, gender identity, gender expression, national origin, ancestry, citizenship, veteran status, and any other legally protected status under federal, state or local anti-discrimination laws.

The pay range for this position is: $85,000 - $100,000. This is the pay range the Company believes it will pay for this position at this time. Consistent with applicable law, compensation will be determined based on the skills, job-related knowledge, qualifications, and experience of the applicant along with the requirements of the position, and the Company reserves the right to modify this pay range at any time. For this role, the Company will offer medical coverage, dental, vision, disability, 401k, and paid time off.

Job Summary

JOB TYPE

Full Time

SALARY

$94k-112k (estimate)

POST DATE

12/21/2023

EXPIRATION DATE

05/04/2024

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