About you:
In this Technical role, you will be responsible for the transfer of new products from engineering and assay development into manufacturing, designing, and developing assembly processes that assure the consistent and cost-effective production of high-quality, repeatable assemblies in prototypes through manufacturing scale-up and steady-state production in a cGMP environment. This will include investigating and assessing different assembly processes, developing, implementing, and maintaining processes and automated equipment for the prototyping, scale-up and production of sub-assemblies, and final assemblies incorporating reagents with molded plastic components. Developing process flow maps and optimal assembly sequences, based on the application of lean principles, as well as investigating, evaluating, and recommending new processes and equipment, Make/Buy recommendations, and transferring to third-party vendors as appropriate.
What you'll do:
Execute the transfer of manufacturing processes and technologies from Research and Process Development groups into a cGMP environment;
Design the appropriate manufacturing processes, define and conduct process development activities and provide design transfer inputs required as part of Tech Transfer;
As the manufacturing Subject Matter Expert, identify potential risks, evaluate impacts of manufacturing process steps and raw materials on product performance, and develop risk mitigations as part of the tech transfer and scale-up;
Interface with Engineering teams to define and establish manufacturing and inventory control processes for reagents, consumables, and instruments;
Support the Assay Development and Engineering teams to ensure the manufacture and supply of prototype consumable assemblies needed for assay design verification and clinical validation activities;
Establish appropriate manufacturing processes and controls to create and maintain consistency and quality of manufacturing from prototype through production scale-up;
Utilize your knowledge and experience to develop, assess, implement, and continually enhance cGMP manufacturing processes and operations;
Lead comprehensive validation activities including planning and execution of validation protocols for equipment, facilities, and processes;
Identification, procurement, installation, qualification (IQ, OQ, PQ), and maintenance of critical manufacturing equipment;
Create and maintain cGMP manufacturing documentation (e.g. Work Instructions, in-process, and final acceptance plans and records);
Support the creation and maintenance of Standard Operating Procedures (SOPs) for ISO13485 and cGMP processes;
Perform Root Cause Analysis of manufacturing failures, in collaboration with cross-functional team members, to determine failure causes, and define and implement improvements to address the causes of failures;
Drive Continuous Improvement in manufacturing by identifying improvement opportunities and developing and implementing process improvements.
What you need:
Bachelor’s degree in STEM;
5+ years of significant manufacturing engineering and/or operational experience in Diagnostics or smilar industries combining biologicals and reagents with injection molded components;
Demonstrated critical thinking and analytical reasoning skills;
Ability to apply a disciplined engineering approach to define and execute designed experiments, analyze data as well as define problems, collect data, establish facts, and draw valid conclusions;
Familiarity with the manufacturing of reagents, consumables, and instruments for IVDs, validation/qualification requirements, and cGMP processes;
Excellent communication skills and attention to detail;
Strong organizational skills and ability to multitask across projects and activities;
Proven ability to collaborate and work effectively with cross-functional teams.
Bonus points for:
Six Sigma and/or Lean certification with demonstrated experience in applying the tools and methodologies to real-life practical situations;
Familiarity with global IVD regulations related to manufacturing;
Prior experience with high-volume automated assembly processes;
Experience with Project Management and leading project teams;
An appreciation of puns!
About Vital
Vital is revolutionizing point-of-care diagnostics with our groundbreaking platform, VitalOne, designed to deliver real-time care wherever patients are. Our mission is to democratize technology that puts people in control of their health, making healthcare more accessible and proactive.
We've built a dynamic, global team of experts across various disciplines including chemistry, software, engineering, and microfluidics. At Vital, we thrive on change, operate on trust, and leverage the diversity of perspectives in everything we do. We push key decisions to folks on the front lines, fostering a culture fundamentally rooted in having a growth mindset.
We seek tenacious, bold, and enthusiastic individuals ready to create impactful change in the healthcare industry. At Vital, you will make a difference; your talent and energy will be valued, and your life's best work will be possible. Together, we're working at a rapid pace to transform healthcare, ensuring that everyone has access to the care they need, when and where they need it.
Join us in our mission to revolutionize healthcare and make a lasting impact on people's lives.
Vital Biosciences Inc. is an equal opportunity employer and values diversity in the workplace. We are therefore happy to accommodate any individual needs in keeping with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act. If you require accommodation in order to participate in our hiring process, please contact us to make your needs known in advance.
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