Senior Quality Assurance Engineer Salary at The Common Application Inc BETA

Business Unit: Cubic Integrated Supply Chain Company Details: When you join Cubic, you become part of a company that creates and delivers technology solutions in transportation to make people's lives easier by simplifying their daily journeys, and defense capabilities to help promote mission success and safety for those who serve their nation. Led by our talented teams around the world, Cubic is committed to solving global issues through innovation and service to our customers and partners. We have a top-tier portfolio of businesses, including Cubic Transportation Systems (CTS) and Cubic Defense (CD). Explore more on Cubic.com. Job Details: Job Summary: Responsible for helping the company achieve its financial goals and objectives through the implementation of various strategies and initiatives. The strategies and initiatives should align with company goals and support growth, increased market share, and competitiveness. Oversees manufacturing, purchasing, inventory control and manufac

Job Title: Quality Assurance Analyst Department: Quality Engineering Reporting to: VP of Quality Engineering Location:Baltimore, MD (Not Remote: In-Office at least 3-days per week) Hours of work: Typical hours of work are from 8:30 AM until 5:30 PM Monday through Friday. Additional hours may be necessary as needed. This position is eligible for overtime; any hours worked over 40 in a week will be compensated at 1.5 times the hourly rate. Compensation: $19.25 per hour, which annualizes to approximately $40,040. Overview: We are looking for Quality Assurance Analysts to join InVita's Transplant Division and team of passionate and brilliant visionaries who are transforming cloud-based medical software and enabling millions of lives to be saved and healed around the globe. The Quality Assurance Analyst executes testing procedures to ensure that software meets established quality standards. They will be responsible for preparing test plans, test cases and protocols to test logic, error hand

Position Overview: This position will be responsible for planning, organizing, and overseeing Elutia’s Quality strategy to ensure the timely delivery of safe and effective products that meet all regulatory and compliance requirements. This role will ensure that processes required for the Quality Management System(s) are effectively established, implemented, maintained, and will proactively develop improved processes to comply with the requirements of 21 CFR Parts 820 (Medical Devices) and 1271 (Human Cells, Tissues, and Cellular and Tissue). This person will also lead the Quality team and work closely the key partners, including Operations, R&D and Regulatory to support Elutia in achieving its strategic goals of Humanizing Medicine through its current and future product platforms. This position will be located on-site in the Company’s new Gaithersburg, MD facility. Essential Duties & Responsibilities: Serve as the senior Quality leader within the company, and as a business leader. Unde

Job Description Job Description Title: Project Manager – Cybersecurity, Cloud Design, System Engineering Location: Washington, D.C. metro area Summary Rios Partners is a mission-driven consulting firm creating positive change by delivering value for our clients, investing in our employees, and solving tough problems that benefit our local and global communities. We ground our approach in empathy, enabling our team members to better hear our customers’ challenges and work together to develop effective solutions. As a team, we know what it takes to move organizations forward with measurable, sustainable results.   Our primary consideration when evaluating candidates is alignment with our Mission and Values, which can be found at  http://www.riospartners.com/mission-and-values/.  Job Description As a Project Manager at Rios Partners, you will play a crucial role in driving the successful delivery of projects that align with our mission of creating positive change and delivering value for

Medcura, Inc. is a leading innovator in advanced medical devices, with a specialization in polymeric materials, both natural and synthetic. We are committed to developing life-saving technologies that redefine standards in medical treatment. As we expand, we are seeking a Head of Manufacturing / Site Lead to oversee our headquarters' manufacturing operations and drive excellence in our production capabilities. Role Summary and Key Responsibilities The Head of Manufacturing / Site Lead will be responsible for the overall leadership and strategic direction of Medcura's manufacturing operations. This role is pivotal in ensuring efficiency, compliance, and scalability in production processes, with a strong emphasis on polymeric medical devices. The ideal candidate will bring deep expertise in medical device manufacturing, with at least 10 years of experience, and a background in chemical or biomedical engineering. Strategic Leadership: Oversee and direct manufacturing operations at Medcura

**Manager, Quality Systems Audit** **Position Summary** Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalents Harmans/BWI, MD facility is a FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies. The campus features two manufacturing facilities: The Harmans/BWI-1 EMA and FDA approved facility, at approximately 200,000 sq. ft., houses 10 CGMP manufacturing suites, fill/finish, central services, testing labs, and a warehouse. The Harmans/BWI-2 facility, at approximately 145,000 sq. ft., is under development and will house 8 CGMP manufacturing suites and cold storage warehousing. Both facilities support Phase 3 through commercial manufacturing of advanced therapeutic products including AAV and other viral vector-based thera

Position Title: Sr. Quality Engineer Location: Baltimore, MD (Area) Department: Quality Assurance Reports To: Director of Quality The Ideal Candidate will have 10+ YOE focused on ISO quality within a manufacturing environment. Compensation: Highly competitive salary + bonus STI Full Benefits, Medical, Dental, Vision, 401K Matching, Life Outstanding company culture and vertical career mobility Quality Systems & Compliance Manage and maintain quality documentation for the Quality Management System (QMS), including procedures, work instructions, and audit materials. Ensure organizational compliance with applicable quality standards such as ISO 9001, ISO 13485, and AS9100. Participate in and support internal, customer, and third-party audits, including supplier audits and regulatory reviews. Inspection & Testing Develop and execute inspection protocols, sampling plans, and test methodologies. Perform and oversee First Article Inspections (FAI), in-process inspections, and final product val

CBNA, a Bouygues Construction Company, is looking for a Senior QA/QC Engineer with Civil Works experience to join the Potomac River Tunnel Project in Washington, DC. You will be supporting the Design-Builder’s QAQC Manager in the establishment, implementation, and maintenance of the Design-Builder’s Quality Management System (QMS) to the Contract requirements. About CBNA : At CBNA, we have been delivering large-scale projects such as the groundbreaking Port of Miami Tunnel and Pawtucket Tunnel CSO in Rhode Island. Our expertise extends throughout underground works, river and maritime works, linear projects, signature bridges and industrial civil engineering. The Potomac River Tunnel project is a landmark initiative under the Clean Rivers Project. The project aims to construct a nearly 5.5 miles tunnel beneath the Potomac River with 2 different TBM, serving as a critical infrastructure element to control combined sewer overflows. This will significantly enhance the water quality of the