Associate Structural Engineer - Healthcare

Are you an experienced structural engineer with a passion for healthcare? Join the UK team of our Global Healthcare Division to tackle complex sustainability and engineering challenges. If you are driven to create meaningful change that positively impacts society and the environment, this role is tailor-made for you.As an Associate Structural Engineer, you will play a pivotal role in bridging the gap towards a sustainable future, working alongside a team committed to excellence. Your RoleIn this position, you will integrate into our expanding UK Healthcare Team, focusing on client engagement, business development, and managing key accounts. Your expertise will guide the delivery of innovative advisory and design solutions within the healthcare sector across the UK, with opportunities to contribute internationally.You will enjoy flexible working arrangements, allowing you to work from any of our primary offices or from home. Our portfolio includes exciting projects such as Hillerod Hospital in Denmark, Cambridge Children’s Hospital, Royal Marsden, and Shrewsbury & Telford Women and Children’s Hospital.Your key responsibilities will include:Leading and developing a team of Structural Engineers within the UK Healthcare Team.Managing your own projects and ensuring the highest standards of design work from initial concept to detailed execution.Acting as a structural engineering project manager, coordinating resources and tasks to meet project deadlines.Collaborating with multidisciplinary teams, including MEP, civil, and geotechnical engineers.Enhancing the reputation of the UK Healthcare Team through quality work and innovative solutions.Developing structural engineering concepts and design philosophies.Representing Ramboll at project meetings with clients and collaborators.Effectively communicating designs with team members and construction sites.Implementing best practices for delivering sustainable and innovative design services.Conducting site visits to support design development and review ongoing contract work.Actively participating in technical groups to foster continuous improvement.Driving team improvement initiatives. Your TeamYou will join a vibrant and growing team known for making a significant impact through our work. Collaborating with leading UK and international architects, we pride ourselves on our innovative approach, supported by our Scandinavian design heritage.

Join our innovative team at Ramboll, where we are seeking a passionate and detail-oriented Structural Engineer specializing in healthcare projects. In this role, you will collaborate with multidisciplinary teams to design safe and sustainable structures that enhance patient care and meet the evolving needs of healthcare facilities. You will have the opportunity to work on exciting projects that make a difference in communities.

Join our dynamic team at Ramboll as a Structural Engineer specializing in building structures across multiple levels. We are seeking a passionate individual who is eager to tackle complex engineering challenges and contribute to innovative designs that enhance the built environment. You will collaborate closely with architects, contractors, and other engineering disciplines to ensure the successful execution of projects.Your expertise will play a vital role in delivering high-quality solutions, optimizing structural performance, and adhering to industry standards. This role offers the opportunity to work on a diverse portfolio of projects while advancing your professional development in a supportive environment.

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.

Amylyx Pharmaceuticals is dedicated to pioneering innovative treatments for diseases with significant unmet needs. We view challenges as opportunities, driving our mission with urgency, robust scientific inquiry, and a steadfast commitment to the communities we serve. As a clinical-stage company, we focus on addressing conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is powered by our talented team, guided by core values of audacity, curiosity, authenticity, engagement, and accountability—fostering a culture of care. We are assembling an experienced group of individuals ready to take meaningful action, as the communities we support cannot afford to wait. If you share this passion and are committed to addressing some of the toughest challenges in medicine, we invite you to explore this exciting opportunity and apply.The OpportunityThe Associate Director of Healthcare Professional Marketing will play a pivotal role within our Marketing team, spearheading the healthcare professional (HCP) engagement strategy for the launch of avexitide aimed at treating post-bariatric hypoglycemia (PBH). This position will concentrate on identifying, understanding, and engaging key segments of HCPs, including thought leaders and early adopters, to enhance awareness of PBH and the therapeutic role of avexitide. This individual will collaborate closely with our sales force and field-facing teams, including Thought Leader Liaisons (TLLs), to ensure aligned, educational, and impactful engagement with the HCP community. Through the development of tailored promotional strategies and educational initiatives, you will enhance the HCP's comprehension of PBH, promote informed clinical discussions, and facilitate successful product adoption at launch.This is a remarkable opportunity for a strategic, collaborative, and results-driven HCP marketer to establish a high-impact engagement platform in a complex and underserved therapeutic landscape.

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.

Imagine... being part of an innovative organization that cultivates and develops life sciences companies dedicated to pioneering groundbreaking technologies aimed at revolutionizing health care and sustainability. Company Overview Expedition Medicines is a dynamic, privately held, early-stage biotechnology company at the forefront of the Protein Editing field. We specialize in creating small molecules that modify protein structure and function to target currently undruggable options across various therapeutic strategies. Our advanced platform combines cutting-edge small molecule chemistry and chemoproteomic discovery technologies with Machine Learning (ML) to facilitate generative design. Backed by Flagship Pioneering, we leverage their vision, courage, and resources to propel Expedition Medicines from platform validation to impactful patient solutions. We seek passionate, collaborative, and determined problem solvers to join our mission! Role Overview: The Senior/Principal Scientist in Structural Biology will concentrate on determining protein-ligand complex structures using X-ray crystallography and cryo-electron microscopy (cryo-EM). This role involves delivering structural insights and collaborating with project teams to advance structure-based drug design and uncover the mechanisms of action of small molecules. Key Responsibilities: Design and implement structural biology strategies for multiple projects. Oversee the design, expression, and purification of protein constructs for structural determination. Develop and execute protocols to achieve high-quality crystals for X-ray crystallography. Create and implement protocols for grid optimization, data collection, and analysis in cryo-EM. Refine and communicate structures of protein-ligand complexes, collaborating with project teams to drive hit-to-lead and lead optimization processes. Manage contract research organizations (CROs) to ensure efficient delivery of protein expression and structural biology services. Enhance our capabilities and serve as a trusted authority in the field of structural biology.

Lila Sciences seeks an Associate Engineer to join the Research Operations team in Cambridge, MA. This team develops high-throughput methods that support scientific discovery across multiple disciplines. The position centers on hands-on work with materials characterization, using advanced tools such as spectroscopy and microscopy. This role provides direct exposure to automation technologies while supporting projects that influence the company’s direction. It suits candidates interested in expanding their engineering skills and building a strong base in scientific operations. Key responsibilities Perform materials characterization using SEMXRF, XRD, Optical Microscopy, Nanoindentation, and Profilometry. Prepare reagents, solutions, electrolytes, samples, and consumables to support experiments across shifts. Follow standard operating procedures to maintain accuracy and consistency. Monitor workflow, troubleshoot routine issues, and escalate concerns to keep operations steady between shifts. Record and organize experimental data with care. Identify and suggest ways to improve efficiency and streamline shift operations. Report unusual results or observations to scientists for review. Collaborate with scientists and engineers on projects spanning life sciences and physical sciences. Location This position is based in Cambridge, MA, USA.

AbbVie is seeking a highly skilled Associate Director to lead our Safety Operations Portfolio. This pivotal role involves overseeing safety operations while ensuring compliance with regulatory requirements. The ideal candidate will possess exceptional leadership skills and a strong background in pharmacovigilance.Join our dynamic team and contribute to advancing healthcare solutions that enhance patient safety and improve health outcomes. This is an exciting opportunity for professionals looking to make a meaningful impact in the pharmaceutical industry.

We are seeking a dedicated and innovative Associate Scientist specializing in Neurology to join our dynamic team. In this role, you will contribute to cutting-edge research projects that aim to advance our understanding of neurological disorders. You will collaborate with experienced scientists and researchers, utilizing state-of-the-art technologies and methodologies.Key responsibilities include conducting experiments, analyzing data, and contributing to scientific publications. If you are passionate about neuroscience and eager to make a significant impact in the field, we would love to hear from you!

Join our dynamic team at Integrated Resources, Inc. as an Associate Director of Pharmacovigilance. In this pivotal role, you will oversee the safety and efficacy of pharmaceutical products, ensuring compliance with regulatory standards and advancing our commitment to patient safety.Your expertise in pharmacovigilance will guide our strategic initiatives, collaborating with cross-functional teams to enhance product safety and regulatory submission processes.

We are seeking a highly skilled Associate Director of Drug Safety and Pharmacovigilance to join our dynamic team at Nuvalent. This pivotal role involves overseeing drug safety operations, ensuring compliance with regulatory requirements, and enhancing the pharmacovigilance strategy. The ideal candidate will possess a deep understanding of drug safety processes and a passion for advancing patient safety in the pharmaceutical industry.

Join Integrated Resources Inc. as a Clinical Associate, where you will play a vital role in supporting our budgeting and forecasting efforts within the healthcare sector. We are looking for a detail-oriented professional who is passionate about improving healthcare outcomes through effective financial analysis.

Join Integrated Resources Inc. as a Senior Drug Safety Associate and contribute to the vital field of drug safety and pharmacovigilance. In this role, you will play a key part in monitoring and ensuring the safety of pharmaceutical products, working closely with cross-functional teams to assess risk and implement safety measures.

Amylyx Pharmaceuticals is on a bold mission to revolutionize the treatment of diseases that have significant unmet needs. While others may see obstacles, we actively pursue opportunities with urgency, rigorous scientific methods, and a steadfast commitment to the communities we serve. As a clinical-stage company, we are currently targeting conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is driven by our talented team, united by core values that include being audacious, curious, authentic, engaged, and accountable, fostering a culture of compassion. At Amylyx, we have assembled a highly experienced group dedicated to action, as the communities we serve cannot afford to wait. If you share our passion and are committed to addressing some of the most challenging problems in medicine, we invite you to explore this opportunity and apply.The OpportunityThe Clinical Data Management team at Amylyx Pharmaceuticals is in search of an Associate Director, Clinical Data Programmer. In this role, you will collaborate across functions to deliver hands-on data management support, programming expertise, and technical leadership. You will be responsible for developing, maintaining, and validating clinical databases, as well as executing computer programs to access, visualize, and report clinical trial data, adhering to clinical plans, ICH guidelines, and regulatory standards. As the Associate Director of Clinical Data Programming, proficiency in programming languages is essential for creating both textual and graphical representations that facilitate data cleaning and review.

Join our dynamic team as a Medical Information Associate II where you will play a pivotal role in providing accurate and timely medical information support. This is an excellent opportunity for entry-level professionals eager to start their career in the healthcare industry. You will be responsible for responding to inquiries, ensuring compliance with company policies, and contributing to the overall efficiency of our medical information services.

About eGenesiseGenesis is an innovative clinical-stage biotechnology company dedicated to developing human-compatible engineered organs to tackle the critical global organ shortage. Our proprietary genome engineering platform facilitates extensive, multiplex gene edits aimed at removing major biological barriers, incorporating protective human transgenes, and inactivating endogenous retroviruses. Our flagship program, EGEN-2784, a genetically engineered porcine kidney, is currently undergoing evaluation in a multi-patient Expanded Access study at Massachusetts General Hospital (MGH). Headquartered in the vibrant city of Cambridge, MA, eGenesis is at the forefront of pioneering medical solutions.As the Lead Clinical Research Associate, you will spearhead site monitoring activities and oversee Clinical Research Associates (CRAs) for designated clinical trials. Collaborating closely with Clinical Operations leadership and cross-functional teams, you will ensure that studies are executed in strict adherence to protocols, ICH-GCP guidelines, regulatory requirements, and our company Standard Operating Procedures (SOPs).

COMPANY DESCRIPTION We are a pioneering start-up dedicated to transforming the landscape of chemical discovery. Our innovative platform integrates artificial intelligence with a state-of-the-art laboratory discovery pipeline to redefine molecular formulation development. Our interdisciplinary team is exploring uncharted chemical territories, facilitating significant advancements in drug delivery, agricultural formulations, and sustainable, high-performance industrial chemicals. Backed by Flagship Pioneering, a leader in biotechnology origination, we have fostered over 115 scientific ventures in 25 years, generating more than $20 billion in aggregate value, 500+ patents, and over 50 clinical trials for groundbreaking therapeutic agents. THE ROLE We are on the lookout for a passionate and skilled Senior Research Associate or Associate Scientist to enhance our formulation discovery platform by characterizing biomolecules. This position involves utilizing a range of biophysical and biochemical methodologies to analyze the effects of formulations on biomolecular integrity, aggregation, and functional stability. You will collaborate closely with chemists and machine-learning experts to produce high-quality experimental data that drives formulation design and predictive modeling initiatives. The ideal candidate will possess a solid background in biochemistry, structural biology, or biopolymer engineering, complemented by practical experience with analytical instrumentation for biomolecular characterization. KEY RESPONSIBILITIES Conduct experiments assessing biomolecular stability and solubility across various formulation conditions. Evaluate cargo structural integrity and folding utilizing circular dichroism (CD) spectroscopy and complementary biophysical techniques. Measure biomolecular interactions and stability through spectroscopy, dynamic light scattering, and electrophoretic methods. Prepare samples for diverse external workflows to evaluate molecular integrity and degradation. Experimental Pipeline Support Collaborate with formulation chemists to investigate cargo-formulation interactions across different experimental contexts. Generate high-quality experimental datasets to assist internal modeling and data analysis processes. Support laboratory instrumentation maintenance and troubleshooting. Maintain organized laboratory records, analyze results, and communicate findings effectively to cross-functional teams.

THE ROLE As an Associate or Senior Associate within Molly Gibson’s Pioneering Business Unit (PBU) at Flagship Pioneering, you will engage in the ideation, research, and refinement of innovative venture hypotheses. Your primary responsibilities will include validating critical biological and technological unknowns and transforming rigorously tested concepts into a NewCo centered on scientific advancements. You will play a pivotal role in the origination of the company, encompassing the early stages of identifying and recruiting essential partners and advisors, establishing foundational intellectual property, leading the recruitment of the initial scientific team, and fostering a productive team culture. In this position, you will collaborate with stakeholders across the expansive Flagship ecosystem to leverage comprehensive support for your ventures. A successful candidate will become the authority on the foundational science of the enterprise, articulate and frame the strategic direction, and translate this strategy into actionable plans, operationalizing them alongside a Principal or Partner from the venture creation team.

Join our dynamic team at Integrated Resources Inc. as a Senior Neurology Research Associate, where you will play a pivotal role in advancing groundbreaking research in neurology. You will collaborate with top-tier professionals, contributing to innovative projects that drive the future of neurological health.