Program Manager, Research & Development Quality Assurance - GCP

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.

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.

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.

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.

Join our dynamic team at Integrated Resources Inc. as a Quality Assurance Documentation Associate! In this pivotal role, you will be responsible for ensuring the accuracy and quality of our documentation processes. Your keen attention to detail and commitment to excellence will help us maintain high standards in our quality assurance practices.

Office location: Cambridge, UK – This is a hybrid role that will require some working days from our Cambridge office, with the specific schedule to be coordinated with your line manager. Candidates should be located within a reasonable commuting distance or be willing to relocate as necessary.Are you an experienced QA Analyst with a passion for open-world gameplay systems and a commitment to enhancing high-quality player experiences?As a Quality Assurance Analyst on RuneScape: Dragonwilds, you will play an integral role in ensuring the stability, performance, and enjoyment of our expansive open-world survival crafting game. You will collaborate closely with developers, designers, and producers to test complex gameplay systems, proactively identifying quality risks, and ensuring that new features perform as intended across various platforms.Your responsibilities will include taking ownership of feature testing, mentoring junior team members, and continuously refining our QA processes. This position is perfect for someone with console and PC testing experience who is adept at navigating the challenges of open-world QA and eager to enhance their technical and collaborative abilities. Key Responsibilities:Develop a comprehensive understanding of new and evolving features while providing insightful feedback on design and quality aspects.Design and implement structured test plans across gameplay systems, including survival mechanics, AI, crafting, exploration, and environmental interactions.Document and communicate defects clearly and concisely, providing actionable insights along with steps to reproduce, severity levels, and potential impacts.Engage in test strategy discussions to evaluate system interactions, identify coverage gaps, and address quality risks.Conduct various testing types, including functional, regression, compatibility, and performance testing on both console and PC builds.Contribute to the assessment and enhancement of QA tools and workflows.Analyze defect trends and test outcomes to pinpoint patterns or coverage deficiencies.Work closely with development teams to clarify feature intentions, verify fixes, and ensure quality alignment.Provide informed contributions to bug triage and task prioritization discussions based on testing impacts and player experiences.Mentor and support junior testers informally, sharing knowledge and reviewing testing outputs.Maintain and update test documentation and knowledge bases, identifying gaps as necessary.Take ownership of testing for specific features or systems, diligently tracking progress and reporting risks.Build specialized expertise in selected gameplay or technical areas, establishing yourself as a go-to QA contact for those systems.

Scholar Rock is a leading biopharmaceutical firm dedicated to discovering, developing, and delivering transformative therapies for individuals suffering from serious diseases with significant unmet needs. As a pioneer in the understanding of the transforming growth factor beta (TGFβ) superfamily of proteins, we are named for the resemblance of a scholar rock to protein structures. Our clinical-stage organization is committed to advancing groundbreaking treatments where protein growth factors play a crucial role. Over the past decade, we have built a robust pipeline aimed at enhancing the standard of care for neuromuscular diseases, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted treatments can have a profound impact. Scholar Rock stands out as the only company that has demonstrated clinical proof of concept for a muscle-targeted therapy in spinal muscular atrophy (SMA). Our dedication to pioneering innovative therapeutic approaches is driven by the extensive application of our proprietary platform, which has developed novel monoclonal antibodies to selectively modulate protein growth factors with remarkable precision. By leveraging advanced science in areas historically underserved by conventional therapies, Scholar Rock is consistently working to unlock new possibilities for patients. Discover more about our approach at ScholarRock.com and follow us on @ScholarRock and LinkedIn.Position Overview:We are in search of a highly skilled and driven Senior Director of US Quality Assurance to join our team. Reporting directly to the Head of Global Quality, this role will provide both strategic and operational leadership for US Quality Assurance. A strong emphasis will be placed on managing external partner governance, implementing quality risk management strategies, and establishing a scalable quality infrastructure to support our development through commercialization efforts.

We are seeking a seasoned Senior Lead Quality Assurance Analyst to join our dynamic team in Cambridge. In this pivotal role, you will lead QA initiatives, ensuring that our products meet the highest standards of quality and performance. You will collaborate closely with cross-functional teams to develop effective testing strategies and oversee the implementation of quality assurance processes.

Join our dynamic team at Integrated Resources Inc. as a Senior Lead Quality Assurance Analyst, where you will play a crucial role in ensuring the highest quality of our software products. In this leadership position, you will oversee QA processes, mentor team members, and collaborate with cross-functional teams to enhance our testing strategies.Your expertise will guide the development of test plans, execution of test cases, and the implementation of best practices in QA methodologies. We are looking for a passionate individual who thrives in a fast-paced environment and is committed to delivering exceptional software quality.

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.

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.

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 Steritech as a Food Safety and Compliance SpecialistLocation: Cambridge, OntarioSteritech is a leader in food safety and quality assurance, serving as a trusted partner to some of the most recognized brands across various sectors including manufacturing, food service, retail, and hospitality. Our mission is to empower clients to deliver the safest and healthiest experiences to their customers. As part of the Rentokil Terminix family, we uphold the highest standards in food safety and compliance.Your Future Starts Here! At Steritech, we are dedicated to fostering a culture of continuous learning and professional growth. With a majority of our management team having advanced from specialist roles, we believe in nurturing talent from within. Joining our team means embarking on a career path filled with opportunities for advancement. We equip you with the necessary tools, resources, and mentorship to ensure your success, as we recognize that your achievements contribute to our collective success.As a Food Safety & Compliance Specialist, you will partner with clients in the hotel, restaurant, and grocery sectors to ensure adherence to brand standards, food quality, and exceptional service.Key Responsibilities:Conduct thorough assessments to evaluate compliance with regulatory, industry, and proprietary standards.Monitor food preparation and cooking practices to uphold food safety and sanitation standards.Collaborate with clients to identify and address the root causes of discrepancies in assessments while developing corrective action plans.Educate and guide clients on creating a safer and healthier workplace for their employees and customers.Willingness to travel up to 50% of the time by car and/or plane, approximately 10 overnight stays per month.

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.

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 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.

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.

Join Luminance, the innovator in Legal-Grade™ AI technology for enterprises. Supported by prestigious venture capitalists and recognized in the Forbes AI 50 as one of the 'Most Promising Private AI Companies in the World' and in Inc. 5000’s list of 'Fastest Growing Companies in America', Luminance is revolutionizing the legal sector globally.We are seeking detail-oriented and analytical individuals to become part of our newly formed Quality team. You will play a crucial role in developing and upholding an advanced Quality Assurance (QA) process designed to ensure our product meets the expectations and needs of our users. If you are passionate about this opportunity but feel that your qualifications do not perfectly match the requirements, we encourage you to apply. At Luminance, we are committed to fostering an inclusive workplace where everyone can thrive. Your enthusiasm is the most important trait we look for in applicants!

We are seeking a highly skilled Software Testing Manager to lead our testing team in Cambridge, MA. In this role, you will oversee the development and execution of testing strategies, ensuring the delivery of high-quality software products. You will collaborate with cross-functional teams to identify testing requirements, develop robust testing plans, and enhance the overall testing process.