About Us:
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:
We are seeking a motivated and detail-oriented Quality Assurance Technician to join our team in supporting hands-on quality-related activities in the laboratory and provide manufacturing operations support, primarily focused on quality control inspections and testing. This position offers a unique opportunity to bridge the gap between scientific innovation and regulatory compliance, contributing to the development of high-quality products through cross functional collaboration.
Job Duties & Responsibilities:
- Perform inspections across all stages of production
- Perform inspections of raw materials and incoming inventory
- Interact with manufacturing department to ensure inspections are completed in a timely manner
- Prepare and maintain test data for review
- Generate non-conforming material reports as required
- Communicate quality or compliance concerns with urgency
- Maintain quality testing and trending program
- Assist in quality monitoring and measurement system
- Perform Quality Assurance testing in support of product development as needed
- Assist in maintenance of calibration system and equipment
- Performs additional quality duties as assigned
- Identify areas for quality control improvement and implement new methods accordingly
Job Requirements:
- High school diploma, GED, or relevant work experience
- 2-5 years of inspection and/or production experience in a regulatory or controlled environment (ex. medical device, pharmaceutical, biomedical industry, or diagnostic laboratory setting
- Excellent organizational skill and attention to detail
- Strong written and verbal communication skills
- Proficient in Microsoft Office
- Familiarity with quality measuring instruments (ex. calipers, pipettes, balances, and general lab equipment)
- Experience working in a clean room environment preferred
- Ability to work independently and prioritize responsibilities to meet deadlines
- Demonstrated ability to analyze and interpret information
Working Conditions:
- Long periods of time working on a computer
- The ability to complete physical and visual inspections
- Ability to lift up to 25 lbs
- Ability to work in an Environmentally Controlled Area (ECA) or lab setting
