Staff / Principal Engineer, Technical Mitigations Research

Join Lila Sciences as a Staff or Principal Engineer specializing in Technical Mitigations Research. This role offers an exciting opportunity to leverage your engineering expertise to develop innovative solutions in the field of technical mitigations.

Join our team as a Regulatory Affairs Specialist where you will play a crucial role in ensuring compliance with regulations and standards within the industry. You will collaborate with cross-functional teams to prepare, review, and submit regulatory documents to relevant authorities, ensuring timely approvals for our products. Your expertise will contribute to the overall success and safety of our operations.

Your Impact at Lila Sciences Lila Sciences is on the lookout for a highly skilled Staff/Principal Mechanical Engineer to enhance our Hardware & Controls Engineering team. The specific title—Staff or Principal—will align with your level of experience and expertise. As a pivotal technical leader, you will apply your extensive knowledge to design and develop components for workcell robotics, mechanical systems, and automation within the realms of life sciences and physical sciences. You'll collaborate with a diverse team of experimental scientists, AI/ML specialists, software engineers, and process automation experts to spearhead intricate projects, mentor multidisciplinary teams, and deliver cutting-edge automation solutions. What You Will Be Creating Oversee the design and execution of bench-scale robotics and mechanical systems for advanced automation in life science and physical science applications. Craft innovative pneumatic, electro-mechanical, and optical solutions tailored for state-of-the-art robotic workcells utilized in biological research and materials discovery. Lead and mentor teams in advanced CAD design and analyses using SolidWorks, optimizing systems for high-throughput workflows. Manage the creation and validation of designs through rapid prototyping techniques such as 3D printing and laser cutting. Facilitate cross-functional collaborations to seamlessly integrate mechanical designs with software and controls across scientific fields. Devise strategies to convert manual processes into automated workflows while adhering to stringent safety and quality standards. Coordinate with external suppliers for bespoke component development and system integration. What You Need to Succeed A Bachelor's or Master's degree in Mechanical Engineering, Robotics, or a related discipline. 8+ years of mechanical engineering experience, showcasing proven expertise in life science and physical science automation (title will be aligned with experience & expertise). Extensive proficiency in SolidWorks CAD design, GD&T, and DFMA methodologies. In-depth experience utilizing requirement management systems, product lifecycle management, and product data management systems. Proven leadership in managing complex projects and mentoring engineering teams. Bonus Points For Significant experience in automation across scientific disciplines, with a strong command of SolidWorks CAD design, PDM, and related technologies.

Amylyx Pharmaceuticals is on a bold mission to revolutionize the treatment of diseases with significant unmet needs. Where others perceive obstacles, we recognize opportunities that we pursue with a sense of urgency, scientific rigor, and steadfast dedication to the communities we serve. Our focus is currently on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission thrives on the commitment of our team. Our core values—be audacious, be curious, be authentic, be engaged, and be accountable—foster a culture of care. At Amylyx, we have assembled a highly skilled team eager to take decisive action because the communities we support cannot afford to wait. If you share our enthusiasm and are committed to addressing some of the most challenging problems in medicine, we invite you to explore the opportunity below and submit your application.The OpportunityThe Director of Clinical Sciences will play a pivotal role within the Clinical Development team, providing essential scientific guidance for ongoing projects. This position reports to a Medical Director and involves cross-functional collaboration with R&D, program management, clinical operations, biostatistics, and data management. The candidate will support and propel key developmental efforts for clinical studies and the execution of the overall Clinical Development Plans (CDP).

Harvard University is seeking a highly skilled and visionary Director of Construction and Capital Programs. This pivotal role involves overseeing and managing the planning, design, and implementation of construction projects across the university's campuses. The ideal candidate will have a deep understanding of construction management principles, exceptional leadership skills, and the ability to collaborate effectively with various stakeholders.The Director will be responsible for ensuring that all projects are completed on time, within budget, and to the highest quality standards. You will lead a team of professionals, drive strategic initiatives, and play a crucial role in shaping the future of Harvard's infrastructure.

Join Lila Sciences as a Research Associate specializing in Protein Science and Cell Free Expression. In this dynamic role, you will contribute to groundbreaking research, collaborating with a talented team to develop innovative solutions in protein production and expression technologies.

Location: Cambridge, UK – This role offers flexible working arrangements, primarily focusing on remote work. Candidates should either be located within a reasonable commuting distance from our office or be open to relocation for necessary onsite attendance.This is an 18-month fixed-term contract.Are you ready to be at the nexus of technology, data, and strategic decision-making, where your insights directly influence funding and project execution?Reporting directly to the Associate Director of Strategic Portfolio Management, you will oversee the daily delivery of Jagex’s technical and data projects. Your role is crucial in maintaining an accurate portfolio view that provides leadership with clear insights into delivery health, dependencies, risks, and commercial implications, enabling informed prioritization. By bridging technical execution with commercial strategy, you will facilitate the resolution of complex programs, highlight trade-offs, and ensure that our most valuable projects progress smoothly with transparency.Key Responsibilities:Manage Jagex’s technical and data portfolio, ensuring timelines, milestones, dependencies, and ownership details are accurate to enable confident prioritization by leadership.Coordinate commercial, technology, and data plans, making sure sequencing and resource allocation are optimized to deliver the most impactful results first.Provide structure to priority technical initiatives, ensuring clarity and coordination so that delivery remains focused, timely, and results-oriented.Identify and address blockages or delays early, facilitating rapid intervention to present options and trade-offs that enable decision-making and regain momentum.Proactively oversee cross-portfolio risks and dependencies to minimize surprises, allowing teams to execute effectively without constant crisis management.Deliver a single, trustworthy view of delivery health, converting technical progress into business and financial outcomes for executive and board discussions.Promote collaboration and clarify ownership across teams, closing any data gaps to ensure everyone operates from a unified perspective.Enhance our portfolio practices and tools, boosting transparency and governance to increase delivery confidence continuously.

Company Overview: Korro Bio is a pioneering biopharmaceutical company dedicated to the development of innovative genetic medicines targeting both rare and common diseases through its proprietary RNA editing technology. Our mission is to revolutionize the field of genetic medicine by utilizing RNA editing to create precise and temporary modifications at the RNA level rather than DNA, thereby enhancing specificity and long-term tolerability. With a portfolio of unique programs, we aim to leverage our expertise in oligonucleotide-based approaches to deliver therapies that improve patient outcomes. Based in Cambridge, Massachusetts, we are committed to combining cutting-edge science with a collaborative spirit to achieve transformative results in human health.At Korro, we thrive on collaboration, driven by our vision to create impactful genetic solutions for widespread health challenges. Our core values—Rewrite the Future, On the Cutting Edge, Better Together, Dynamically Different, Kindness and Integrity—are woven into every aspect of our work culture, guiding our hiring practices and daily interactions. Join our team to help redefine the possibilities in genetic medicine and contribute to lasting health advancements.Position Overview: We are searching for a Senior Scientist to enhance our growing CMC team at Korro Bio. This role will involve overseeing the management of CMO analytical labs as well as the development of analytical methods, impurity characterization, degradation pathway analysis, and the transfer, qualification, and validation of methods for RNA-based therapies. You will play a crucial role in maintaining the quality and stability of drug substances and products throughout their development lifecycle. Collaborating closely with cross-functional teams and external partners, you will ensure that analytical data meets regulatory filing requirements and supports clinical trial progress.

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.

As the Senior Technical Product Manager for the EverQuote Remarketing Platform, you will play a pivotal role in bridging the gap between insurance shoppers and providers through effective Email and SMS communication. You will spearhead transformative growth at EverQuote by implementing innovative technology solutions that are central to our core mission and key revenue-generating opportunities. At EverQuote, our Technical Product Managers are inquisitive self-starters who are dedicated to achieving business results through technology. While your focus will be on more technical products and customer needs, your approach will remain customer-centric, ensuring alignment with our broader business objectives. In this role, you will be responsible for envisioning, designing, and delivering technical product innovations and tools that facilitate essential business operations for remarketing and re-engaging our shoppers. You will own the roadmap, adoption, operation, business value, and lifecycle of our Email and SMS platforms. Your role will involve nurturing relationships with both technical and non-technical users of your technology, collaborating with stakeholders to develop and execute strategies that maximize business outcomes. A data-driven mindset will guide your discussions, and you will build partnerships across various teams including Product Managers, Engineers, Architects, Analysts, and Business stakeholders. You will also define key metrics to assess progress and the value of your outputs, providing regular visibility to senior leadership on all facets of your product(s). In this dynamic position, you should be comfortable with ambiguity and possess a strong sense of ownership to create a structured approach for delivering results within our remarketing initiatives. Your analytical abilities and exceptional problem-solving skills will be vital. Clear and proactive communication, both oral and written, will enable you to excel in managing stakeholder relationships. You will have a robust background in Product Management, experience with software agile development cycles, and a track record of managing and delivering large cross-functional programs. You will thrive in a collaborative environment, able to respond to escalations with data and technical analysis. This is a hybrid role requiring presence in the office several days a week.

Director of Business Development - USVCLS: Accelerating the Path to PatientsSince 1997, VCLS has been at the forefront of supporting innovators in biotech, Medtech, and Healthtech on their journey from discovery to market. We have a simple yet ambitious mission: to accelerate the delivery of life-changing products to patients. With over 230 industry experts globally, we are dedicated to our long-term vision of delivering 500 new healthtech products by 2050.We are currently on the lookout for a Director of Business Development - US—an experienced, hands-on leader—to implement our US commercial strategy with clarity, intention, and urgency. This role is perfect for an individual who views business development as a consultative art rather than just a transactional process, characterized by curiosity, empathy, and a genuine passion for Life Sciences.Key Results & AccountabilitiesDriving Growth Through Consultative Partnerships Propel significant revenue growth by cultivating strong, trust-based relationships within the biotech, medtech, healthtech, and investment sectors. Take charge of the complete business development lifecycle including listening, identifying opportunities, crafting solutions, and securing strategic partnerships. Exhibit total ownership of the sales process ensuring every client feels comprehensively understood and supported without any handoffs or gaps.Excellence in Client Engagement & Sales OwnershipThis role is committed to delivering a world-class consultative experience, anchored in scientific curiosity and deep client insight: Actively listen and convert client challenges into clear, actionable opportunities. Ensure that clients connect with the right VCLS experts at the right time to maximize value. Coordinate internal teams to facilitate meaningful discussions rather than generic interactions. Lead the development of proposals with meticulous attention, ensuring that each reflects a deep understanding and tailored solutions. Maintain outstanding responsiveness, clarity, and follow-through throughout the client engagement journey.Market Presence & Brand Elevation Represent VCLS credibly and passionately across the US market. Establish a prominent presence at industry events, within accelerators, investor networks, and innovation hubs. Enhance VCLS’s reputation as a reliable partner in regulatory strategy, clinical development, CMC, evidence generation, and commercialization.Stakeholder Leadership & Internal Alignment Collaborate closely with Business Unit leaders, scientific experts, and senior management to ensure seamless execution of business development initiatives. Encourage cross-functional teamwork to optimize client outcomes.

Join our dynamic team as a Clinical Trial Leader, where you will be at the forefront of innovative clinical research. You will be responsible for overseeing the planning, execution, and management of clinical trials, ensuring compliance with all regulatory requirements and organizational standards. Your leadership will guide cross-functional teams to deliver high-quality results, contributing to the advancement of healthcare solutions.

We are seeking a passionate and innovative Computational Biologist to join our dynamic team in Cambridge, MA. In this role, you will utilize advanced computational techniques to analyze biological data and contribute to groundbreaking research and development projects in the life sciences. You will collaborate closely with cross-functional teams to drive the integration of computational models with experimental data, ultimately advancing our understanding of complex biological systems.

As an Associate Scientist III, you will play a crucial role in advancing our scientific research initiatives. You will collaborate with cross-functional teams to design, execute, and analyze experiments that contribute to our innovative projects. Your expertise will help drive our mission forward, ensuring that we continue to push the boundaries of scientific discovery.

Join Integrated Resources, Inc. as a Pharmacovigilance Scientist and contribute to the safety and efficacy of pharmaceutical products. In this role, you will be responsible for monitoring, assessing, and reporting adverse effects associated with drug therapies. Your expertise will directly impact patient safety and regulatory compliance while collaborating with cross-functional teams.

Join our innovative team as a Senior Scientist where you'll drive critical research projects and make a significant impact in the field. We are seeking a highly motivated individual with a passion for scientific discovery and a strong background in relevant disciplines.

Join Integrated Resources, Inc. as a Pharmaceutical Research Associate, where you will play a vital role in advancing medical research and drug development. You will collaborate with a team of scientists and researchers to assist in the design and execution of clinical trials, ensuring the integrity and accuracy of data collection.Your contributions will help pave the way for innovative therapies that make a difference in patients' lives. Ideal candidates are detail-oriented, possess strong analytical skills, and have a passion for the pharmaceutical industry.

As the Chief of Staff to the CEO at TetraScience, you will play a pivotal role in driving strategic initiatives and operational excellence. You will be a trusted advisor, facilitating effective communication between the CEO and various stakeholders while managing key projects and priorities. Your leadership will be vital in shaping the company’s vision and ensuring alignment across all functions.

Isomorphic Labs is hiring a Head of Translational Sciences, Drug Design for its Cambridge, MA site. This senior leader will guide the translational strategy across the drug discovery portfolio, working closely with teams at the intersection of biology, artificial intelligence, and medicine. The position plays a central role in shaping how new therapies are advanced and how disease mechanisms are understood within the organization. Role overview This leadership role focuses on driving translational approaches for drug design. The Head of Translational Sciences will collaborate with colleagues to advance projects from early discovery through clinical evaluation. The team’s work includes strengthening biological insights into disease, supporting the selection of drug targets, and developing biomarkers to track pharmacodynamic effects and target engagement in clinical studies. Translational Sciences at Isomorphic Labs The Translational Sciences group in Boston is essential to the company’s mission. This team informs critical decisions across the portfolio, guiding projects through various stages of research and development. Close collaboration with other teams ensures that scientific progress benefits from both biological expertise and AI-driven insights. Company background Founded in 2021, Isomorphic Labs (IsoLabs) builds on the breakthroughs of the AlphaFold system. The company brings together drug discovery experts and machine learning specialists to develop predictive and generative AI models that accelerate scientific progress. The team uses AI to model complex biological systems, design new therapeutic molecules, and pursue treatments for challenging diseases. Ongoing innovation in model architecture supports work across diverse therapeutic areas and modalities. Culture Isomorphic Labs values interdisciplinary collaboration and a supportive environment. Every team member contributes to the shared goal of addressing serious diseases through AI-driven science and digital biology.

Join Lila Sciences as a Senior Research Associate or Associate Scientist in the Protein Science department, focusing on our cutting-edge Antibody Platform. You will play a crucial role in advancing our research initiatives, contributing to the development of innovative antibody-based therapeutics. This position offers the opportunity to collaborate with a talented team dedicated to scientific excellence and the pursuit of transformative solutions in healthcare.