Quality Engineer II

Pramand-LL; Bedford (MA); On-site; USD 70,000 - 100,000; Full time

Job summary

Pramand, LLC, based in Bedford, MA, is seeking a Quality Engineer II to support QA/QC for implantable medical devices. You will lead day-to-day quality activities, participate in design controls, and ensure compliance with cGMP, ISO 13485, and 21 CFR Part 820.

You will collaborate with manufacturing and R&D to maintain robust process controls, perform root-cause analysis, and contribute to continuous improvement initiatives in a regulated environment.

Qualifications

• Bachelor’s degree in scientific/engineering or equivalent work experience.
• 2–4 years of experience in a regulatory and/or controlled environment (medical device/pharma/biomedical).
• Excellent organizational skills and attention to detail.
• Strong technical background, scientific judgment, customer focus, initiative.
• Familiar with FDA QMSR and ISO 13485 requirements.

Responsibilities

• Manufacturing Quality Support: establish quality standards, inspection protocols, and real-time QA aid to manufacturing.
• Design & Development Support: assist with verification/validation activities and design changes as needed.
• Quality System & Compliance: support cGMP, ISO 13485, CAPA, audit trails and regulatory requirements.
• General: collaborate across teams to resolve issues and drive corrective actions.
• Quality metrics tracking for continuous improvement.

Skills

Quality Assurance

Quality Control

Root Cause Analysis

CAPA

Documentation

FDA QMSR

ISO 13485

MS Office

Excel

Education

Bachelor's degree in scientific/engineering

Tools

MS Office

Excel

Job description

AboutUs:

Pramand, LLC, is a medical device company based in Bedford, MA. We develop implantable medical devices from novel, proprietary hydrogel materials that improve patient outcomes while lowering the cost of therapy. We self-fund our projects through preclinical development and work with financial partners for clinical development and commercialization. Our portfolio of hydrogel technology positions us to be the leader in creating new hydrogel based medical devices to address unmet medical needs in a range of surgical interventions. We have launched over ten medical device companies based on this unique technology. These companies have generated over $4B in value and have helped over 5 million patients worldwide achieve better outcomes.

Position Summary:

The Quality Engineer II is an intermediate level role. They will serve as a technical team member performing day-to-day quality assurance, quality control and quality engineering activities for medical devices. This individual will be involved with leading technical aspects of low complexity projects, supporting manufacturing, participation in operational excellence and quality documentation.

Job Responsibilities:

Manufacturing Quality Support

• Develops, implements, and maintains quality standards and inspection protocols for raw materials and manufacturing processes.
• Conduct and document incoming, in-process, and final inspection activities.
• Provide real-time QA support to manufacturing operations, including inspections, inventory control, document reviews, and quality issue investigations (root cause analysis).
• Identify possible sources of manufacturing defects and assisting in dispositioning of non-conforming material.
• Identify, implement, and manage equipment calibrations to support production goals
• Partner with manufacturing and R&D teams to ensure robust process controls and adherence to quality standards.

Design & Development Support

• Support product verification and validation activities, including testing for new product development and sustaining programs
• Support quality assurance initiatives in areas such as design controls, qualifications, and validation activities.
• Support changes to design specifications

Quality System & Compliance

• Assist in maintaining compliance with internal procedures and external standards and regulations, including cGMP, ISO 13485 and 21CFR Part 820.
• Support quality system functions such as non-conformance reporting, CAPA (Corrective and Preventative Actions), complaint handling, calibration control, and environmental compliance.
• Track, analyze, and report on key quality metrics to drive continuous improvement initiatives

General

• Collaborate with cross-functional teams to drive issue resolution and implement effective corrective and preventative measures
• Customer / supplier liaison contact
• Moderate-complexity problem solving with some creativity
• Performs additional quality duties as assigned

Job Qualifications & Requirements:

• Bachelor’s degree in scientific/engineering or relevant discipline or equivalent work experience.
• 2-4 years of experience in a regulatory and/or controlled environment, i.e. medical device, pharmaceutical, biomedical industry or a diagnostic laboratory setting.
• Excellent organizational skills and attention to detail.
• Must have a strong technical background, scientific judgement, customer focus, exhibits initiative.
• Excellent communication skills, problem solving and time management skills.
• Self-oriented, self-organized and able to work with minimum supervision.
• Experience working in clean room preferred.
• Computer literacy, proficiency in MS Office, Excel, PowerPoint etc.
• Knowledgeable in application of quality principles and industry guidelines for quality systems.
• Excellent interpersonal skills and ability to work collaboratively in a cross-functional team setting.
• Understanding of FDA QMSR and/or ISO 13485 requirements.