Senior Quality Engineer

Portal Instruments is redefining how advanced injectable therapies are delivered.

Founded on MIT research, Portal develops innovative drug-delivery platforms that enable patients to self-administer complex biologics safely, comfortably, and reliably.

Our lead platform, PRIME Nexus®, is

a reusable, software-tunable drug-delivery system designed to support high-viscosity and large-volume injectables, with both needle-assisted and needle-free delivery options depending on therapeutic needs.

Portal partners with biopharmaceutical companies and key players in the medical device ecosystem to integrate our delivery platforms into drug–device combination products that improve patient experience, reduce cost of goods, and support successful commercialization. Guided by human-factors science, rigorous engineering, and real-world usability, Portal is building the next generation of

patient-centric drug delivery solutions.

Title:

Senior Quality Engineer

Reports to:

QA Manager

Location:

Hybrid (Primary location: Boston/Cambridge, MA)

This role is a critical part of Portal’s mission to advance PRIME Nexus® toward commercialization. You will work cross-functionally with engineering, regulatory, manufacturing, and external partners to help

scale a novel drug-delivery platform that directly impacts patient experience and therapeutic success.

This role will support quality processes for medical device development and manufacturing at Portal Instruments. The QE will represent Quality on internal and external project teams for both design and manufacturing. This role will support quality systems, document control, product design verification & validation, manufacturing process validation, customer feedback, and corrective and preventive action investigations and implementation.

This is an opportunity to take ownership, solve complex problems, and contribute meaningfully at a pivotal stage of Portal’s growth.

• Contribute directly to the development, validation, and commercialization of Portal’s drug-delivery platforms

• Collaborate across disciplines to solve complex technical and operational challenges and translate requirements into practical, compliant solutions

• Support new product development and product realization through all design control phases.
• Support verification & validation (test plans, protocols, reports), test method validation, incoming inspection, lot release of engineering, clinical and commercial devices, nonconforming product disposition, review of design documentation, calibration and equipment validation

(IQ/OQ/PQ)

• Support risk management file generation and maintenance for Portal Instruments products throughout their lifecycle.
• Collaborate with cross-functional teams on design and process related risk management activities.
• Administer Portal’s online document management system and oversee creation, issuance, maintenance, and retention of controlled documents and records
• Support origination and release of Engineering Change Orders
• Support continuous improvement of quality system procedures in accordance with 21 CFR 820, ISO 13485, EU MDR, MDSAP, and ISO 14971

• Apply statistical methods and process design tools to establish test plans as well as evaluate test data and establish process control

• Lead or participate in corrective and preventive processes as required, including documentation of CAPA, root cause investigation, and implementation of improvement activities

• Conduct and/or participate in internal and external audits as needed
• Partner cross-functionally to translate quality requirements into practical, compliant solutions
• Act as subject matter expert for quality engineering practices
• Partner with Engineering and Operations to…