5 design manager document controller jobs at 5 companies in Boston, MA

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Document Controls Manager
Boston, Massachusetts, United States
$140k-$155k/yr OnsiteFull Time
WSP
WSPTSX: WSP: Global engineering and professional services consulting firm.
7+ YOE7+ years document control experience on design/construction projects; bachelor\u0002s degree or equivalent; EDMS implementation experience; e-Builder or InEight certification; advanced MS Office and SharePoint skills; supervisory experience.
Microsoft SharePoint, Procore, e-Builder, Bluebeam, InEight, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Visio, MS Office
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Senior Project Manager
Newton, Massachusetts, United States
OnsiteFull Time
Magnendo
Magnendo: Medical device startup developing robotic navigation systems for neurovascular stroke and aneurysm procedures.
5+ YOE5+ years project/program management in medical-device or regulated-product development, experience with cross-functional and external partner coordination, knowledge of design controls, risk management, V&V, and regulated documentation; trained in PMP/CAPM/PMI-ACP/SAFe/Lean/Six Sigma or equivalent.
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Commercial Management Coordinator
Boston, Massachusetts, United States
OnsiteFull Time
HDR
HDR: Global professional services firm specializing in architecture, engineering, and construction.
3+ YOE3+ years in A/E, design-build, P3, project management, or project controls; experience with contract management, risk, document control, claims, and project accounting; QuickBase/low-code a plus; up to 10% travel.
QuickBase
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Sr Controls Engineer
Cambridge, Massachusetts, United States
OnsiteFull Time
Lila Sciences
Lila Sciences: Builds AI and autonomous labs for scientific discovery.
4+ YOE4+ years designing complex control systems for automated labs; expertise with PLC/HMI/SCADA, industrial networking, robotics integration, engineering documentation, and vendor management.
PLC, SCADA, HMI, AutoCAD, SolidWorks Electrical, TwinCAT, Python, C++, OPC-UA, MQTT, REST, AWS
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Quality Assurance Specialist II, Device Engineering
Woburn, Massachusetts, United States
$85k-$105k/yr OnsiteFull Time
Terrestrial Bio
Terrestrial Bio: Private U.S. biotechnology developing needle-free microarray patches for delivering GLP-1 medicines, vaccines, and other therapies.
4+ YOERequires 4–5 years of quality experience in a cGMP-regulated medical device, pharmaceutical, biologics, or combination product environment, plus ISO 13485, FDA QSR, design controls, risk management, validation, and GMP documentation experience.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Quality Management System (QMS), Design History File (DHF), Design Verification and Validation (DVV), Failure Mode and Effects Analysis (FMEA), Test Method Validation (TMV), Process Validation (PV), Corrective and Preventive Action (CAPA)