Company Overview At Motorola Solutions, we believe that everything starts with our people. We're a global close-knit community, united by the relentless pursuit to help keep people safer everywhere. Our critical communications, video security and command center technologies support public safety agencies and enterprises alike, enabling the coordination that's critical for safer communities, safer schools, safer hospitals and safer businesses. Connect with a career that matters, and help us buil

Title: Project Engineer No. of Positions: 1 Hiring Mode: Contract (TP) Location: 22 Cherry Hill Dr, Danvers, MA-01923 [Onsite] Job Description: Key Responsibilities- Collaborates with the agile team to translate the business vision into language that can be consumed by development resources.Develop and manage the software design history fileSupport Project Documentation and Materials needs via SAPMaintain JAMA tool and produce required documentation for the design history fileTrack project perf

Role : Medical Devices Project EngineerLocation: Danvers, MA-01923 [Onsite] Skills: JAMA , Medical devices ,FDA , SaaS , Agile Minimum of 1 year experience in the medical device industry as well as Medical Device Software systems and cardiovascular devices highly preferred (Class medical device experience strongly preferred)Demonstrates knowledge of quality policies, principles and best practices and FDA/ISO requirementsExperience supporting FDA regulated productsProject Management Profession

Role: Product Security Engineer Hiring Mode: Contract (TP) Location: Danvers, MA-01923 [On-site] Skills Matrix Skill Last Used Experience in Years/month Rating (10 points) 1 = newbie 10 = expert Hands on Exp. Yes/No Security risk management techniques Regulatory standards and compliance frameworks (e.g., NIST Cybersecurity Framework,ISO27001, SOC2, HIPAA, GDPR) Pre-market product development activities Medical devices FDA Job Description: 5+ years industry experience in Information Security.Wor

Key Responsibilities: Collaborates with the agile team to translate the business vision into language that can be consumed by development resources.Develop and manage the software design history fileSupport Project Documentation and Materials needs via SAPMaintain JAMA tool and produce required documentation for the design history fileTrack project performance, specifically to analyze the successful completion of short- and long-term goalsMeet budgetary objectives and make adjustments to project

Experis IT ManpowerGroup has partnered with a leading Medical Device Company in the Burlington, MA for a Product Surveillance Analyst role to assist their team. This is an on-site role. Industry: Medical Device Company Title: Product Surveillance Analyst Location: Burlington, MA Duration: 12 months Shift: M-F 8am-5pm JOB DESCRIPTION Duties: May perform multiple functions within the postmarket surveillance department. Major responsibilities would include determining classification, review, and

Are you ready to build America's energy future? Form Energy is an American manufacturing and energy technology company. We're revolutionizing energy storage with cost-effective, multi-day technology designed to keep the electric grid secure and reliable, even during extended periods of stress. By strengthening the electric system and reimagining what's possible, we're giving clean energy a whole new form! In recent years, Form Energy has earned a number of accolades, including being named by TIM

Are you ready to build America's energy future? Form Energy is an American manufacturing and energy technology company. We're revolutionizing energy storage with cost-effective, multi-day technology designed to keep the electric grid secure and reliable, even during extended periods of stress. By strengthening the electric system and reimagining what's possible, we're giving clean energy a whole new form! In recent years, Form Energy has earned a number of accolades, including being named by TIM

This is a medical technology company that specializes in building devices to help patients improve their overall wellbeing and health. They are currently hiring a fulltime Product Manager to work on their transcranial magnetic stimulation (TMS) products. Which is a FDA-cleared for the treatment of depression. The TMS technology uses Magnetic Stimulation aimed at key areas of the brain involved in emotional regulation, cognitive function, and self-control. By activating neural pathways, it helps

Who we are With its A.I.-powered robotic technology platform, Symbotic is changing the way consumer goods move through the supply chain. Intelligent software orchestrates advanced robots in a high-density, end-to-end system - reinventing warehouse automation for increased efficiency, speed and flexibility. What we need We are looking for a talented Senior Mechanical Engineer to join our Strategic Projects team within our Core Engineering Org. In this role you will contribute to the entire prod

Role: Product Security EngineerLocation: Danvers, MA-01923 [On-site] Security risk management techniquesRegulatory standards and compliance frameworks (e.g., NIST Cybersecurity Framework,ISO27001, SOC2, HIPAA, GDPR)Pre-market product development activitiesMedical devicesFDA 5+ years industry experience in Information Security. Working knowledge of regulatory standards and compliance frameworks (e.g., NIST Cybersecurity Framework,ISO27001, SOC2, HIPAA, GDPR). Experience with security risk managem

Piper Companies is seeking a Senior Quality Assurance Manager to lead quality assurance efforts for a medical device facility in Chelmsford, MA through a M-F Onsite work schedule. The Senior Quality Assurance Manager is pivotal in ensuring compliance with regulatory standards and driving continuous improvement initiatives. Responsibilities of the Senior Quality Assurance Manager include: Lead quality assurance for two products: balloon pump and balloon catheter. Develop and execute QA strategie

Senior Associate Scientist - Pharmaceutical Sciences (CMC) Location: Remote/Hybrid - East Coast preferred | ? Contract Position Competitive hourly rate| Biologics | mRNA | Gene Therapy iO Associates is currently working with an exciting and highly innovative biotech organization at the forefront of next-generation RNA therapeutics. While this position is not live yet, we are actively building a talent pipeline for an upcoming contract opportunity and would love to connect with professionals wh

Job Description: Maintenance Technician "To become the world?s greatest baker, we need the world?s greatest team members!" What FGF Offers: FGF believes in Home Grown Talent, accelerated career growth with leadership training, unleashing your potentialCompetitive Compensation, Health & Welfare Benefits including Vision & Dental and flexible options at competitive premiums401k matching programDiscount program - Restaurants, gyms, shopping, etc.Tuition reimbursement Overview: FGF Brands is growi

Leidos' Security Enterprise Solutions (SES) operation is seeking a Senior Software Engineer (C++) in Tewksbury, MA to join our cross-functional engineering team using cutting edge technology to develop truly novel solutions that make travel and trade safer, healthier, and more efficient on a global level. This individual will be apart of supporting our next generation CT X-Ray products. We are seeking local candidates in the Tewksbury, MA area that can work onsite full time (Day Shift). We are o

Schneider Electric IT Corporation seeks a Senior Manager Firmware Engineering in Andover, MA. Job Description: As an individual contributor, provide critical expertise to team of firmware engineers to develop real-time embedded firmware to control power electronics and communications for Uninterruptible Power Supplies. Define firmware architectures and roadmaps for firmware development. Assist in talent acquisition of new firmware engineers. Mentor new team members on legacy code base and sub s

PREREQUISITES BS/BA degree in Scientific Discipline (Masters or higher preferred) with 5+ years in the pharmaceutical industry, preferably with 3+ years CMC regulatory experience, Sterile Injectable experience preferred. Responsibilities will include, but are not limited to, the following: 1. Participate in the development of the CMC regulatory strategy for post-approval small molecule product submissions, including global supplements/variations and responses to health authority queries. 2. Prep

Title : Human Factors Engineer (Medical Devices) Location : Andover, MA ( Hybrid ) About the job We are seeking an experienced Human Factors Engineer for a 4-month contract. This role requires hands-on experience conducting usability studies with detailed Word reports (not just PowerPoint). The ideal candidate will have a strong background in authoring risk analysis documents, demonstrating proactive communication, and providing active follow-ups. The candidate should be detail-oriented and or

5+ years of Workday Financials configuration and integration experience (AP/AR, Fixed Asset Management, Reporting)Strong familiarity with Workday s Financial Data Model (FDM)Solid understanding of enterprise data migration and ETL processesEffective communicator comfortable working across multiple teams and partner agencies

A medical device manufacturer and distributor in Marlborough is looking for talented Product Managers to join their team. They recently launched a novel FDA approved medical device that is being used to treat impulse control, addiction, and depression. This product has the potential to be revolutionary in the mental wellness space. They are looking for Product Managers who hav a strong background in medical device product management with a background either in biology or biomechanical engineeri