Senior Associate in Controlled Document Management

About the Role Lila Sciences, Inc. is looking for a Controls Engineer in Cambridge, MA. This position focuses on designing and implementing control systems that support the performance and reliability of the company's products. What You Will Do Design control systems for new and existing products Implement and test system functionality to meet performance goals Contribute technical expertise to projects that require reliable, precise control Location This role is based in Cambridge, MA, USA.

Role Overview Lila Sciences is hiring an Engineer II or Senior Mechatronics Engineer for Hardware & Controls Engineering in Cambridge, MA. This position focuses on designing and developing mechatronic systems that support and advance our product line. What You Will Do Design, build, and refine mechatronic systems for new and existing products Work closely with colleagues to improve performance and reliability in engineering projects Apply hardware and controls engineering expertise to solve technical challenges Who We’re Looking For Experienced in mechatronics, hardware, and controls engineering Interested in technology and eager to contribute to collaborative projects Ready to help shape the next generation of our products

Join Engine as a Senior Associate in Community OperationsAt Engine, we empower visionary founders who are tackling the world's most critical challenges in areas such as climate change, health, and advanced technologies. Our commitment includes providing robust support through founder programs, access to shared infrastructure and labs, and the opportunity to connect with a diverse national network of corporate partners, investors, and industry experts.

The Engine supports Tough Tech entrepreneurs who are developing solutions for major global challenges. As a nonprofit, the organization connects founders with infrastructure, funding, and operational support to help turn breakthrough science and technology into real-world impact. Role overview The Chief Growth Officer (CGO) will lead The Engine through its next phase of growth. This executive shapes partnership strategies, drives revenue initiatives, and works to strengthen the organization’s market position. The CGO also serves as a strategic advisor to the CEO and leadership team, providing input on key organizational decisions. Who should apply Experienced leaders with a background in Tough Tech, either as entrepreneurs or commercial executives Individuals with a track record of scaling organizations and launching first-of-a-kind (FOAK) projects Candidates who have advocated for Tough Tech founders and engaged with the broader ecosystem Location This position is based in Cambridge.

Join our dynamic team as a Quality Control Analyst II, where you will play a vital role in ensuring the highest standards of quality in our products. This position is ideal for detail-oriented individuals who are passionate about quality assurance and eager to contribute to the success of our projects.

Join our dynamic team at Turner Townsend as a Cost/Senior Cost Controller in a collaborative hybrid working environment. We are looking for a skilled individual who is adept at managing project costs, ensuring financial accuracy, and providing insightful analysis to enhance decision-making.Your role will involve close collaboration with project teams, offering financial guidance and oversight to ensure projects are delivered on time and within budget. You will leverage your expertise in cost management to facilitate effective financial reporting and forecasting.

Join Alva Energy as a Product Manager specializing in Controls Systems, where you will lead the definition, delivery, and ongoing development of our innovative controls platform, central to our uprate technology. In this pivotal role, you will transform complex, safety-critical engineering challenges into deployable, regulator-compliant products that seamlessly integrate with existing nuclear plant control systems.This position transcends traditional roadmap responsibilities; you will establish a clear vision, articulate detailed requirements, and actively drive engineering execution both internally and with external vendors, ensuring the system's successful implementation in the field. You will serve as the crucial link among controls engineering, vendors, licensing, and plant operations to create a coherent product that delivers tangible value.Key Responsibilities:Own the comprehensive product vision and lifecycle for Alva’s multi-load controls system, overseeing the journey from concept through field deployment and regulatory approval.Translate high-level system objectives (such as load coordination and integration constraints) into clear, actionable product requirements and acceptance criteria.Lead the definition of controls architecture and its interfaces with nuclear plant control systems (e.g., Common Q, Ovation, 7300-class or legacy platforms), ensuring clarity in signal ownership and isolation boundaries.Drive vendor strategy by identifying, evaluating, and managing controls, automation, and integration partners as extensions of the product team.Collaborate with internal engineering teams to ensure alignment of hardware, software, controls logic, and testing plans with product objectives and regulatory requirements.Conduct system-level hazard, failure-mode, and interface risk analyses in partnership with engineering and licensing teams.Coordinate factory, field, and integrated acceptance testing to ensure the product meets performance expectations while preserving existing plant control functions.Engage closely with regulatory and licensing stakeholders to confirm that requirements, setpoints, and implementation strategies are defensible and compliant.Act as the primary decision-maker regarding scope, trade-offs, sequencing, and priorities for the controls system.

We are seeking a dedicated and detail-oriented Quality Control Manager to join our dynamic team at Integrated Resources Inc. in Cambridge, Massachusetts. The ideal candidate will be responsible for ensuring the highest standards of quality across our products and services, implementing rigorous quality management systems, and leading a team of quality assurance professionals.As a Quality Control Manager, you will play a crucial role in driving continuous improvement initiatives and collaborating with cross-functional teams to enhance operational efficiency. Your expertise will help us maintain compliance with industry regulations and exceed customer expectations.

Contract Type: Full-time, PermanentLocation: Cambridge, UKVisa Sponsorship availableJoin Nu Quantum - Innovating the Future of Quantum TechnologyAt Nu Quantum, we are pioneers in the realm of quantum computing and advanced technological solutions, fueled by a passion for innovation, diversity, and excellence. We foster a collaborative environment where talented individuals from various backgrounds unite to redefine the limits of what is achievable.Founded to commercialize a decade's worth of research from the prestigious Cavendish Laboratory, Nu Quantum is dedicated to revolutionizing quantum information systems.Our team is developing groundbreaking technologies that enhance the functionality and speed of quantum computing systems. We are integrating cutting-edge quantum photonic technology to create an efficient and scalable quantum networking infrastructure in collaboration with leading corporations and academic institutions.About the RoleAs a Quantum Control Scientist in our Atomic, Molecular & Optical (AMO) team, you will bridge the gap between physics and engineering, developing and commissioning the real-time control systems that govern our internal trapped-ion quantum processing units.Your work will involve utilizing the ARTIQ platform to create a seamless orchestration of complicated hardware setups. This role encompasses designing and implementing dependable workflows for time-sensitive data acquisition and stabilization protocols, mainly using Python to interface with various systems including custom electronics, lasers, and RF hardware.We seek a creative problem-solver who thrives in a hands-on laboratory setting. Your responsibilities will include developing and optimizing real-time control software that is intricately linked with experimental instrumentation. Collaborating with physicists, engineers, and software developers will be essential, as you contribute to a high-quality, maintainable codebase while ensuring that your solutions are robust, scalable, and future-proof in our rapidly evolving organization.Key ResponsibilitiesDesign and manage real-time orchestration of experimental hardware using the open-source ARTIQ platform.Integrate and control custom hardware (e.g., electronics and FPGA boards), along with third-party hardware, primarily through Python.Monitor experimental parameters and automate their analysis to minimize manual effort and enhance repeatability.Commission, document, and train team members on both hardware and software systems.Work closely with physicists and engineers to achieve technical and performance targets.Create graphical user interfaces for experimental control, real-time monitoring, and data visualization.Collaborate with the software team to standardize workflows, adhering to best practices for maintainable and scalable code.

We are seeking an experienced Project Controls Manager to join our Infrastructure team at Turner Townsend in Cambridge. In this role, you will be responsible for overseeing project controls processes, ensuring timely and accurate reporting, and maintaining project schedules and budgets. Your expertise will contribute to the successful delivery of complex infrastructure projects, while collaborating with diverse teams to drive efficiency and performance.

Scholar Rock is a pioneering biopharmaceutical company dedicated to discovering, developing, and delivering transformative therapies for individuals battling serious diseases with significant unmet needs. Renowned as a global authority in the biology of the transforming growth factor beta (TGFβ) superfamily, our clinical-stage organization is passionately focused on advancing innovative treatments that are fundamentally reliant on protein growth factors. Over the last decade, we have cultivated a robust pipeline aimed at elevating the standard of care for neuromuscular diseases, cardiometabolic disorders, cancer, and various conditions where growth factor-targeted drugs can have a revolutionary impact. Scholar Rock proudly stands as the sole company to have demonstrated clinical proof of concept for a muscle-targeted therapy in spinal muscular atrophy (SMA). Our commitment to unlocking novel therapeutic avenues is driven by the extensive application of a proprietary platform that has developed unique monoclonal antibodies designed to modulate protein growth factors with remarkable precision. By leveraging cutting-edge science in disease areas that have traditionally been overlooked by conventional therapies, we strive each day to create new possibilities for patients. To learn more about our innovative approach, visit ScholarRock.com and follow us on Twitter and LinkedIn.Position Overview:We are actively seeking a highly experienced and driven Senior Director of Global Quality Control to join our team. This pivotal role reports directly to the Head of Global Quality and serves as the senior leader responsible for establishing and maintaining a scalable, phase-appropriate, and inspection-ready global QC strategy across a fully outsourced development and manufacturing network. The Senior Director will provide both strategic and technical leadership for Quality Control activities carried out through external contract laboratories, CMOs, and other testing partners, supporting drug substance, drug product, raw materials, in-process, release, and stability programs.

Join our dynamic team at Turner Townsend as a Project Controls Specialist, where you will be integral to managing planning and control functions across various infrastructure projects. We are seeking passionate individuals at all levels who can contribute to our mission of delivering exceptional project outcomes. You will have the opportunity to work on innovative projects that shape communities and improve lives.

Amylyx Pharmaceuticals Inc. is on a bold mission to innovate the treatment landscape for diseases with significant unmet needs. Instead of viewing challenges as roadblocks, we embrace them as opportunities to advance solutions with urgency, scientific rigor, and a steadfast commitment to the communities we serve. As a clinical-stage company, we are currently addressing conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission thrives on the passion of our people. We embody core values of audacity, curiosity, authenticity, engagement, and accountability, fostering a culture of care. With a seasoned team ready to make impactful changes, we invite you to join us in this endeavor if you share our enthusiasm for tackling some of the most challenging issues in medicine.The OpportunityAmylyx Pharmaceuticals Inc. is seeking a seasoned Senior Director of Chemistry, Manufacturing, and Controls (CMC) to lead our CMC organization in the development of our pipeline, including Phase III synthetic peptide Avexitide and Phase I antisense oligonucleotide AMX0114. The CMC team partners with external CDMOs to implement robust, scalable, and compliant processes for clinical and commercial supply. This role may involve direct leadership or managing leads of internal matrix CMC Asset teams, serving as the CMC representative on Asset program teams. This leader will collaborate across functions to drive technical excellence and ensure CMC alignment with program objectives.The ideal candidate will exhibit strong strategic leadership while actively engaging in hands-on execution as needed. This position reports to the Senior Vice President of Global CMC and External Manufacturing.

Relay Therapeutics is seeking a dynamic and experienced Director of Analytical Development and Quality Control to lead our analytical efforts in drug development. In this leadership role, you will oversee the development and implementation of analytical methods to support our innovative drug discovery pipeline. You will work closely with cross-functional teams to ensure optimal quality control processes and regulatory compliance.Your expertise will play a critical role in driving our mission to improve the lives of patients through cutting-edge therapies.

Join our dynamic team as a Quality Assurance/Quality Control Specialist III. In this pivotal role, you will ensure the highest quality standards are maintained throughout our processes and products. As a QA/QC Specialist, you will be responsible for developing and implementing quality assurance programs, conducting audits, and collaborating with cross-functional teams to drive continuous improvement.

Join our team as a Senior Associate in Controlled Document Management, where you will play a crucial role in managing and maintaining documentation processes. You will be responsible for ensuring compliance with regulatory standards while supporting a collaborative team environment. Your attention to detail and organizational skills will be key in streamlining workflows and enhancing operational efficiency.

Join our dynamic team at Turner Townsend as a Project Controls Specialist, where you will play a critical role in enhancing performance and reporting across various projects. We seek individuals at all experience levels who are passionate about project management and looking to make a significant impact in the Infrastructure sector.

Join our dynamic team at ttp1 as a Mechanical Engineer. In this role, you'll leverage your engineering expertise to design innovative solutions and contribute to exciting projects. Our ideal candidate is a creative problem-solver who thrives in a collaborative environment. If you're passionate about engineering and looking to make a significant impact, we want to hear from you!

Location: Cambridge, UK – This position offers flexible working options, including predominantly remote work. Applicants should be based (or willing to relocate) within a comfortable commuting distance of our office to attend onsite as required.Join us to work on the foundational technologies that drive the RuneScape franchise and contribute to the evolution of Jagex’s platform capabilities!The Game Engine team is tasked with enhancing and optimizing RuneTek, our versatile game engine, with a strong emphasis on rendering technologies that facilitate the development of our gaming platform.As a vital member of the Game Engine Team, you will be instrumental in delivering sophisticated technical solutions, collaborating closely with our production and game development teams to help bring Jagex’s creative vision to life.Your Responsibilities:Enhance and maintain engine technology and shared libraries across core subsystems.Deliver maintainable, production-ready C++ code that aligns with team standards and best practices.Take ownership of features of moderate scope and complexity, from design to completion.Contribute to the creation of scalable, robust, high-availability systems that support live games.Identify and implement performance and workflow enhancements across engine technology.Collaborate effectively within an agile team to deliver business and player value.Assist in evaluating third-party and in-house solutions to determine the best fit.Research and apply cutting-edge technologies to translate innovative ideas into actionable engine improvements.