Compliance Engineer Salary at Astrodyne Tdi Co BETA

Job Summary The Senior Quality Compliance Engineer will work with the Senior Manager of Quality Compliance to ensure Terumo Medical Corporation is achieving compliance to all global regulations and external standards for medical devices, combination medical device/pharmaceutical, and software products through collaborative partnerships and out-reach with cross-functional departments. This includes but is not limited to: FDA 21 CFR Part 820, ISO 13485, EU Medical Device Regulation 745/2017, and MDSAP Country requirements. Job Details/Responsibilities Ensure TMC is effectively monitoring for all new and revised external regulations and standards. Partner with Quality Compliance Process Manager to establish time-bound product plans to conduct gap assessments and remediation activities within the required timeframes. Provide Regulation and Standard Management assistance to the organization as required. Assist management on development, implementation, and maintenance of Quality Performance

Associate Director, Engineering & Automation The Associate Director oversees equipment and system performance in an FDA-regulated manufacturing facility. They lead a team of engineers, ensuring equipment readiness, troubleshooting issues, maintaining compliance, and driving continuous improvement. Key Responsibilities: Oversee day-to-day equipment performance, qualification status, and change controls. Manage utility systems, process/building automation, HVAC, and process equipment. Develop and improve operational strategies, optimizing procedures for existing processes and new product introductions. Coordinate with Project Engineering, Validation, Maintenance, Manufacturing, Process Development, and Quality Assurance. Represent the function to clients, auditors, and inspectors. Direct and approve engineering documentation and reports. Team Leadership & Development: Manage full-time employees and contractors, ensuring proper onboarding, training, and resource allocation. Provide techni

Title: Process Engineer II Location: Morristown, NJ Duration: 12 Months+ Possible Extension Fully onsite Notes: Traveling for the Contingent Worker: We currently have a project that might require travel to Toronto, Canada. Additionally, there might be a need for domestic (US) or European travel based on departmental needs. Typically, this involves one week of travel, sometimes leaving on Sunday and returning on Saturday, depending on the manufacturing schedule. If the travel is to the EU, we will typically leave the US two days before the production start and leave soon after. Required travel to Toronto location for process support, estimated 2-3 times per year (1 week at a time) Open to those willing to relocate at own expense, however local candidates preferred Must have Skills: Bachelor's Degree/Undergraduate Degree or Advanced Degree in Process/Package engineering • Will accept candidate with MS, PHD Degrees Minimum years of 5 years of experience in similar role FDA and EMA Regulat

Job Summary The Development Engineer leads or participates on teams responsible for the design and development of surgical implants and instruments from concept through launch. The focus of these development projects has a heavy emphasis on the individualized treatment of patients on behalf of a requesting surgeon. The role also encompasses implementation of improvements and value engineering to existing patient specific product offerings and services, support of the development of the quality system and other company initiatives. Responsibilities Adhere to Onkos Core Beliefs, Code of Business Conduct, all regulatory requirements and quality standards. Support company advocacy initiatives to help raise awareness of sarcoma and pediatric cancer and drive positive change that will impact the lives of cancer patients. Prepare and manage to comprehensive project plans, resource requirements, project budgets, timelines, etc. Interface with sales force, surgeons, and other stakeholders to un

Job Description: This position is within the functional area of Package Development. Responsibilities: Makes technical and business-based recommendations on primary, secondary and tertiary package systems and material for both new and marketed pharmaceutical product projects. Develops test protocols and manages execution of various packaging studies including USP, EP and transport qualification for bulk and finished drug product and packaging. Acts as technical and coordination focal point for site and external CMO's for multi-site projects regarding technical documentation of package requirements. Define development actives and developed project plans that meet the defined objectives. Acts as Project manager to plan and manage all technical packaging requirements for successful introduction of packages from development stages to commercial market. Identifies new packaging technologies and/or applications that could improve cost, compliance and quality and/or customer acceptance. Exper

About Client: The client provides information technology (IT) services, including business outsourcing, infrastructure technology, and application services. The application service offered by the company includes application development, maintenance, and support. The markets served by the company are financial services and insurance, healthcare, manufacturing, government, transportation, communications, and consumer and retail industries. Rate Range: $40-$45/Hr Job Description: Speech Engineer with Deepgram knowledge mainly on configuration role. Speech Engineer with Development knowledge with creating Algorithms. About ApTask: ApTask is a leading global provider of workforce solutions and talent acquisition services, dedicated to shaping the future of work. As an African American-owned and Veteran-certified company, ApTask offers a comprehensive suite of services, including staffing and recruitment solutions, managed services, IT consulting, and project management. With a focus on exc

Overview: Selective is seeking a Senior engineer responsible for the design, delivery and support of our personal computing environment. Will be a key technical leader to help drive our strategy to Deliver any information, on any device, anywhere. With a strong customer-oriented mindset, responsible for managing key aspects of our virtual desktop packages across the enterprise. Ensure successful maintenance and support for all virtual desktop application installation and deployment across the enterprise. Provide tier 3 technical support on highly complex and technical issues for various desktop, virtual desktop and operating systems. Manage large groups of Windows-based computer systems, utilizing System Center Configuration Manager (SCCM). All job duties and responsibilities must be carried out in compliance with applicable legal and regulatory requirements

Elevate your career at Marotta Controls, a New Jersey Top Workplace three years running! Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the Aerospace & Defense industry. At Marotta, we value bold thinking and teamwork, and we empower our employees to push boundaries while delivering top-tier solutions to our customers. Our team fosters a fun, collaborative culture where creativity and technical excellence thrive! Your next big opportunity starts here. Be part of a company where your work supports a mission that makes a difference—apply today! Engineer II - Mechanical (Commercial Space Systems) Overview The Engineer II - Mechanical is responsible for designing products to meet customer's requirements including all design, functional, material, and test requirements from the customer's component and sub-tier specifications. The specific assignments and responsibilities will be consistent with the level of experience of the engineer. Regular i