Automata is building a world-class company to disrupt the life science industry with our new core products that automate life science workflows across diagnostic, drug discovery and synthetic biology labs. Our mission is to empower scientists with accessible lab automation tools that are fast, flexible, and cost-efficient.

We're helping scientists find cures, map genomes, and diagnose illnesses by building the software they need to design, run and automate their experiments.

To help us on our mission, we’re looking for a Production Quality Engineer to accelerate the product development process and support the business in achieving a fast turnaround of releases.

Why is this role important for Automata?

• Working within the Quality Team you will plan, coordinate and manage the quality assurance and control activities associated with one or multiple product development projects to ensure compliance with internal and external requirements.

• This is an exciting role for a Production Quality Engineer as you will work with the NPI team to support the launch of our new product and drive improvements in operational efficiency.

In this role, you will be:

• Support the Quality Lead in developing and executing a robust quality roadmap

• Interact with technical and operational functions to establish test requirements

• Assist with customer's and supplier's concerns (NCRs/Returns/Warranties)

• Product inspection and validation reports using metrology equipment (CMM, 3d Scanners)

• Lead and/or support Process FMEAs and Control Plans

• Developing Quality Tools (Process Maps, Control Plans, Checklists etc)

• Interact with NPI team towards accurate and repeatable inspection methods

• Ensuring traceability and data records are at the core of the product

• Provide support on process performance (Cp/Cpk) regarding correction and improvement activities

• Support MSA activities during factory acceptance testing

• Preparation and/or review of APQP and PPAP submissions

• Support quality system development and implementation throughout product life cycle

What it takes

• Strong understanding of the Quality Core Tools (APQP, PPAP, FMEA, MSA & SPC)

• Proven experience in developing new processes to assist with product validation

• Aptitude for analysis, organisation and planning

• Technical background in medical, mechanical and/or electrical engineering

• Solid Works and ISO 9001 experience desirable

• Metrology experience using a CMM, Hexagon and/or Romer arm, PC-DMIS software desirable

• Hands on approach

• Ability to work with cross-functional teams

• Knowledge of GD&T and BS8888 Drawing standards

• Great verbal and communication skills

What gets us excited?

We’re passionate about the future of Technology and Automation and our growing success is built upon like-minded individuals who share our passion.

We are excited about building a reliable automation system that will be at the forefront of drug discoveries and more.

If this sounds like a good fit and you have experience with Production Quality you will love having the opportunity to build something that immediately adds value.

What's the process?

• CV review

• Phone interview - 30 mins with Talent

• Online personality assessment - 30min

• Onsite Interview - 2 hours with hiring manager + additional hiring team

• Final Interview - 30 Minutes Culture Round