Controls Engineer

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.

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 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.

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.

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.

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.

Join Integrated Resources, Inc. as a Data Management Quality Associate, where you will play a crucial role in ensuring the integrity and quality of our data management processes. You will collaborate with cross-functional teams to enhance data accuracy and streamline operations.

Join Nuvalent as a Manager in GMP Quality Assurance, where you will play a pivotal role in ensuring the highest quality standards in our manufacturing processes. You will lead a dynamic team, working collaboratively to uphold compliance with regulatory requirements and internal protocols. Your expertise will contribute to our mission of delivering innovative therapies to patients.

We are seeking a highly skilled and experienced Director of Clinical Quality to join our dynamic team at Integrated Resources, Inc. In this pivotal role, you will be responsible for overseeing the clinical quality management systems, ensuring compliance with regulatory standards, and driving continuous improvement in clinical processes.Your leadership will be vital in fostering a culture of quality and safety, collaborating with multidisciplinary teams to enhance patient outcomes and operational efficiency.

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.

We are seeking a highly skilled and detail-oriented Senior Associate specializing in Controlled Document Management to join our dynamic team. In this pivotal role, you will oversee the management, organization, and compliance of critical documentation, ensuring adherence to regulatory standards and internal protocols. Your expertise will contribute to maintaining the integrity and accessibility of essential documents across the organization.

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 highly skilled QA/QC Specialist III to join our dynamic team in Cambridge. In this pivotal role, you will ensure the highest quality standards are met throughout our projects. You will be responsible for developing and implementing quality assurance protocols, conducting audits, and collaborating with cross-functional teams to deliver exceptional results.

Join our dynamic team as a Program Manager in Research & Development Quality Assurance. In this pivotal role, you will oversee the quality assurance processes within the realm of Good Clinical Practice (GCP). Your expertise will be crucial in ensuring that our R&D initiatives meet the highest standards of quality and compliance.As a Program Manager, you will lead cross-functional teams, drive project timelines, and implement effective quality assurance strategies. This position is ideal for a proactive leader who thrives in a fast-paced environment and is passionate about delivering exceptional results in clinical research.

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 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 Integrated Resources, Inc. as a Quality Assurance Specialist. In this pivotal role, you will be responsible for ensuring the quality and performance of our software products through meticulous testing and analysis. You will collaborate closely with development teams to identify issues, recommend improvements, and verify that all features meet our high standards before release.

As a Data Quality Analyst at Integrated Resources, Inc., you will play a pivotal role in ensuring the integrity and accuracy of our data. You will be responsible for analyzing data quality metrics, identifying discrepancies, and implementing solutions to enhance overall data processes. This position is vital for maintaining our commitment to high-quality data standards and supporting data-driven decision-making across the organization.

As a Software Quality Assurance Engineer at Nuclera, you will play a crucial role in ensuring the highest quality standards of our innovative software solutions. You will be responsible for developing and executing test plans, identifying bugs, and collaborating with cross-functional teams to improve our software development processes.