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As the Director of Accounting Operations at Scholar Rock, you will be at the forefront of our financial strategies, leading a dynamic team to enhance our accounting practices. Your expertise will drive the efficiency and accuracy of our financial operations, ensuring compliance with regulations and supporting our growth objectives. You will collaborate with cross-functional teams, providing insightful financial analysis and fostering a culture of financial accountability.
As the Director of Accounting Operations at Scholar Rock, you will be at the forefront of our financial strategies, leading a dynamic team to enhance our accounting practices. Your expertise will drive the efficiency and accuracy of our financial operations, ensuring compliance with regulations and supporting our growth objectives. You will collaborate with …
Integrated Resources Inc. is seeking an experienced Clinical Operations Lead to join our dynamic team in Cambridge, Massachusetts. This pivotal role involves overseeing clinical trial operations, ensuring compliance with regulatory standards, and leading cross-functional teams to achieve project milestones. The ideal candidate will have a strong background in clinical research and a passion for advancing healthcare solutions.
Full-time|$160K/yr - $190K/yr|On-site|Cambridge, MA or New York City, NY
Iterative Health is at the forefront of healthcare technology and services, driving the evolution of clinical research to enhance patient outcomes. Our Site Network features over 70 premier clinical research sites across both the US and Europe, facilitating the rapid development of innovative gastrointestinal (GI) and hepatology therapies. We are dedicated to the success and expansion of our partner sites through the provision of tech-enabled services. By merging extensive clinical trial expertise with state-of-the-art AI technology, we empower research teams and study sponsors to broaden and accelerate access to transformative therapeutics for patients in need.About the RoleWe are on the lookout for a dynamic and driven Director of Operational Finance & Analytics to become an integral part of our expanding team. In this pivotal role, you will collaborate closely with executive leadership, finance, and operational teams to oversee the operational finance aspects of our growing network of research sites and enhance the company’s enterprise analytics capabilities, ensuring precision, consistency, and governance of critical metrics for a reliable single source of truth.Your contributions will be vital in constructing and scaling our Enterprise Data Warehouse (EDW) and executing Adaptive Insights, utilizing these essential systems to provide dependable reporting and forecasting that supports operational decision-making. This hands-on leadership position offers a unique opportunity to make a significant impact as the company evolves.
We are seeking a highly skilled and motivated Contract Clinical Operations Lead to join our dynamic team. In this pivotal role, you will oversee clinical trial operations, ensuring adherence to regulatory requirements and best practices. Your expertise will guide project management, resource allocation, and team coordination, driving the successful execution of clinical studies.
We are seeking an enthusiastic and detail-oriented Accounts Payable Operations Specialist to join our dynamic finance team. In this role, you will be responsible for managing the accounts payable process, ensuring timely and accurate payments to our vendors while maintaining strong relationships with them. You will play a crucial part in supporting the financial operations of our organization.
Join our dynamic team as a Compound Hub Operator at Artech Information Systems LLC in Cambridge, MA. This exciting entry-level position offers a unique opportunity to start your career in a fast-paced environment. As a Compound Hub Operator, you will be responsible for assisting in the operations of our compound hub, ensuring that processes run smoothly and efficiently.
Join Integrated Resources Inc. as a Clinical Operations Lead, where you will play a pivotal role in overseeing clinical trials and operations. You will be responsible for ensuring compliance, managing timelines, and leading a team of professionals dedicated to advancing healthcare solutions. Your expertise will help streamline processes and improve patient outcomes.
Nuvalent seeks an Associate Director of Clinical Operations to join the team in Cambridge, MA or work remotely. This leadership role guides the execution of clinical trials, ensuring every step aligns with regulatory standards and internal protocols. The position partners with cross-functional teams to develop and deliver on clinical strategies, overseeing studies from planning through closeout. What you will do Direct clinical trial operations for multiple concurrent studies Maintain compliance with all regulatory requirements and company procedures Work closely with colleagues across departments to create and implement clinical strategies Supervise all aspects of study management, from initiation to completion Oversee budgets, timelines, and resource planning for clinical programs Mentor and guide junior staff within clinical operations Requirements Significant experience in clinical operations and project management Background working in pharmaceutical or biotechnology organizations Demonstrated ability to manage budgets and timelines Experience mentoring or managing team members
About the Role Plants & Goodwin Inc. is hiring a Heavy Equipment Operator for construction projects in Cambridge. This position plays a key part in running heavy machinery to support ongoing site work. Main Responsibilities Operate equipment such as excavators, bulldozers, and cranes on active construction sites Follow all safety protocols and company procedures while on the job Support project teams by moving materials and preparing work areas as needed What Matters Here Commitment to safe equipment operation Attention to detail when following company standards Ability to work as part of a construction crew
Full-time|$220K/yr - $269.5K/yr|On-site|Cambridge, MA USA
Operating Principal – Summit PBU THE ROLE Join Summit, an innovative Business Unit within Flagship Pioneering, as an Operating Principal dedicated to launching and scaling our NewCos. In this pivotal role, you will oversee operations and strategy across multiple companies, spearhead corporate development efforts, and collaborate closely with scientific leaders to transform groundbreaking ideas into tangible outcomes. This position is perfectly suited for an entrepreneurial leader who excels in uncertain environments, effortlessly navigates between scientific and business realms, and is passionate about building organizations from the ground up to achieve significant growth. KEY RESPONSIBILITIES Lead the strategic and operational planning for one or more NewCos. Drive corporate development initiatives, including partnerships, financing, and strategic alliances, while engaging with the Board of Directors and other key stakeholders. Work directly with scientists and company leaders to align technical advancements with operational objectives. Recruit, mentor, and manage high-performing teams across various functions. Collaborate with Flagship's central teams (Finance, Talent, Legal/IP, HR) to implement best-in-class infrastructure for each company. Develop and execute operational and long-range plans, ensuring timely and budget-compliant achievement of milestones. Establish and maintain strong relationships with investors, partners, and key opinion leaders. PROFESSIONAL EXPERIENCE & QUALIFICATIONS Who you are: You are a dynamic operator and strategist who blends business leadership with scientific insight. You thrive in fast-paced, entrepreneurial settings and are driven by the mission of building organizations that leverage innovative science. Qualifications: 10+ years of experience in biotech, pharmaceuticals, or life sciences strategy/operations; prior management consulting experience is advantageous. Demonstrated success in strategic, operational, or corporate development roles, preferably in early-stage biotech. Strong scientific acumen; ability to rapidly comprehend novel scientific concepts and translate them into actionable plans. Proven track record in assembling and inspiring high-performing teams. Exceptional communication skills, capable of influencing and motivating investors, partners, and internal teams. Proficient problem solver; adept at bringing order to chaos and quickly iterating to find effective solutions. Entrepreneurial, resilient, and hands-on; able to adapt and execute with urgency, unafraid to roll up sleeves and get involved.
We are seeking a highly skilled and experienced Senior Clinical Operations Lead to join our dynamic team in Cambridge. As a pivotal member of our clinical operations team, you will play a critical role in overseeing the planning, execution, and management of clinical trials. Your expertise will ensure adherence to regulatory standards and best practices, while also fostering collaboration across multidisciplinary teams.Your responsibilities will include developing operational strategies, managing budgets, and ensuring timely project delivery. You will also be responsible for mentoring junior staff and facilitating training programs.
Join Harvard University as a Security Manager, reporting to the Director of Safety and Security. In this pivotal role, you will oversee and coordinate security operations, ensuring the safety of staff, visitors, collections, and physical assets at the Harvard Art Museums. As the front-line supervisor, you'll manage security staff during your shifts, applying your expertise with autonomy and sound judgment.Core Responsibilities:Oversee daily security operations at the Harvard Art Museums, managing staffing levels, post coverage, emergency responses, special events, and group visits.Supervise security personnel by scheduling shifts, monitoring performance, providing training, and addressing issues, with a professional approach focused on customer service.Act promptly in emergencies, including medical, fire, and life safety incidents, documenting incidents according to established protocols.Participate in the recruitment and training of new security personnel.Continuously enhance skills to effectively handle a variety of challenges.Optimize resource deployment for efficient operations.Plan daily workflows and support clerical duties, including payroll and timekeeping.Contribute to policy implementation and procedure development for the Security Department, making recommendations to the Director as needed.Assist in creating and applying new security measures to enhance visitor experiences.Utilize Microsoft Office to maintain records, compose communications, and manage statistical databases.Review video footage as needed for investigations and maintain security databases.Support event-related security activities, managing budgets and suggesting operational improvements.
Who is BlueRock?BlueRock Therapeutics LP is a pioneering clinical-stage company focused on advancing cell therapies to develop innovative treatments for individuals affected by neurological and ophthalmic diseases. Our flagship investigational cell therapies, bemdaneprocel (BRT-DA01) aimed at combating Parkinson’s disease and OpCT-001 targeting primary photoreceptor diseases, are at the forefront of clinical research. Established in 2016 through a collaboration between Versant Ventures and Leaps by Bayer, our culture is characterized by a relentless pursuit of excellence, a commitment to transforming medicine, and a strong sense of community and purpose.Our MissionWe leverage foundational scientific principles to facilitate the creation and differentiation of universal pluripotent stem cells into fully functional, authentic cellular therapies capable of addressing a diverse range of diseases. Our capabilities extend to engineering these cells to produce enzymes, antibodies, and various proteins for enhanced therapeutic outcomes.We are dedicated to fulfilling the promise of cellular and gene therapy, revolutionizing the landscape of cellular medicine, and providing new therapeutic options to millions of patients worldwide.We invite collaborative individuals who thrive in a vibrant, dynamic environment and are resolute in their commitment to advancing groundbreaking cellular therapies that profoundly impact patient lives.At BlueRock Therapeutics, we are excited about the ongoing advancements in cellular therapies that can significantly improve the lives of patients across various disease spectra.The Associate Director of Toxicology Operations will play a pivotal role, engaging with both internal and external stakeholders to manage nonclinical study plans that support BlueRock’s development pipeline. This position requires a Program Toxicologist who can effectively utilize their expertise in toxicology to propel the company’s initiatives forward, collaborating closely with program leads and other experts in the field.This role is based in Cambridge, Massachusetts, with a hybrid work arrangement (3 days in the office per week).
Who is BlueRock?BlueRock Therapeutics LP is an innovative clinical-stage biotechnology company specializing in cell therapy. Our mission is to develop groundbreaking medicines for individuals affected by neurological and ophthalmic disorders. Our lead investigational therapies, bemdaneprocel (BRT-DA01) for Parkinson’s disease and OpCT-001 for primary photoreceptor diseases, exemplify our commitment to transforming patient care. Founded in 2016 as a collaboration between Versant Ventures and Leaps by Bayer, our culture is characterized by resilience in the face of challenges, a sense of urgency in advancing medicine, integrity in our mission, and a strong community focus.What Are We Doing?At BlueRock, we leverage cutting-edge science to convert universal pluripotent stem cells into authentic, functional cells for allogeneic therapies targeting a wide range of diseases. Additionally, our engineering capabilities allow these cells to produce therapeutic proteins, enhancing treatment outcomes. Our dedication to cellular and gene therapy is unwavering, and we aim to deliver innovative solutions to millions of patients.We are looking for collaborative individuals who thrive in a vibrant and dynamic work environment, committed to advancing state-of-the-art cellular therapies that will improve patients' lives.The Associate Director of Vendor Management will play a pivotal role in managing and optimizing BlueRock’s essential Development vendor relationships, which are critical for the successful execution of our key clinical initiatives. This position is responsible for ensuring vendor performance, governance, and the overall health of relationships across key outsourced services such as CROs, central labs, imaging, and recruitment vendors.This role sits at the intersection of strategic leadership and operational execution, partnering closely with Clinical Operations, Finance, Procurement, and other functional leaders to ensure that vendors meet their contractual obligations, adapt to evolving program needs, and align with BlueRock’s overarching development strategy. The Associate Director will also be instrumental in establishing scalable, data-driven governance for vendors across Development.
Note: This is a vacation relief position, required to cover vacations and other absences.As a skilled Chiller Operator, you will expertly operate and service chilled water generation and distribution systems as well as associated equipment and components.You will be responsible for maintaining a thorough understanding of these systems, identifying and resolving issues in accordance with industry standards, codes, and university guidelines.Your duties will also include performing various trade skills and responsibilities related to the operation and maintenance of steam equipment, water distribution systems, and other related infrastructure.It is essential to maintain your work area, tools, and equipment according to university standards.You will work independently and collaboratively under the guidance of the Associate Manager or Working Foreman.Job-Specific Responsibilities:Operate the central chilled water plant under varying load conditions.Manage additional plant equipment including water treatment systems and compressed air systems.Collaborate with trades personnel and management to ensure continuous plant operations.Record and analyze critical plant readings essential for operational efficiency and billing (e.g., pressures, temperatures, flows).Complete daily logs, prepare necessary reports, and enter daily information into the computer system.Oversee the chemical treatment program and maintain accurate records.Conduct cleaning and maintenance of plant facilities and assigned boiler areas.Perform inspections and preventive maintenance on various equipment as directed.Operate and maintain various plant systems (including HVAC) to meet operational requirements.Work alongside utility mechanics and carry out other duties as directed.Maintain an organized and clean work environment with tools and equipment.Physical Requirements:Must be able to bend, reach, and maintain awkward postures for extended periods.Capable of lifting up to 75 pounds and assisting with equipment and tool transportation exceeding 300 pounds.Able to push and pull heavy loads as required.Must be comfortable working from ladders, in high places, confined spaces, and on scaffolding.Requires significant walking, climbing, bending, and stooping throughout the workday.
We are seeking a dedicated and knowledgeable Senior Associate in Operational Excellence & Compliance to join our dynamic team at Integrated Resources Inc. In this pivotal role, you will contribute to enhancing our operational processes and ensuring compliance with industry regulations. You will collaborate with cross-functional teams to identify opportunities for improvement and implement best practices that drive operational efficiency.
Full-time|$68K/yr - $78K/yr|On-site|Cambridge, MA USA
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.
Gopuff seeks full-time Operations Associates to join the Cambridge operations team. This position reports to a Site Leader and supports daily warehouse activities that keep the business moving. Role overview Operations Associates play a hands-on role in the warehouse, handling tasks such as picking and packing orders, receiving new inventory, and working closely with delivery riders. Each day brings a mix of responsibilities that help ensure customers receive their essentials quickly and reliably. What we look for Determination and a positive attitude Enjoyment in tackling challenges and solving problems Ability to work collaboratively with team members Creativity and willingness to try new approaches A genuine interest in snacks is a plus About Gopuff Gopuff delivers everyday essentials to customers at any hour, no matter the weather. The company values reliability, innovation, and a drive to reshape retail. Operations Associates are key to making this possible in Cambridge.
Overview: Gopuff is seeking dedicated full-time Operations Associates (OAs) to join our dynamic operations team in Cambridge. Reporting directly to a Site Leader, OAs are vital to our mission and embody qualities such as drive, resilience, positivity, and enthusiasm for overcoming challenges. Your role will encompass various warehouse duties including picking, packing, receiving products, and collaborating with our delivery riders.At Gopuff, we are committed to delivering everyday essentials to our customers—day or night, rain or shine. We are building a team of innovative thinkers, ambitious dreamers, and adventurous risk-takers who are eager to revolutionize the retail landscape at an unprecedented pace. And yes, a love for snacks is a bonus!
Harvard University’s Campus Services - Engineering & Utilities department seeks an Operations and Maintenance Analyst to join the team in Cambridge. This full-time position centers on reviewing and refining operational processes that help ensure reliable and efficient campus services. Key Responsibilities Examine current operations and maintenance procedures to understand existing workflows. Pinpoint opportunities for process improvement and greater efficiency. Contribute to efforts that maintain dependable campus services. Work Environment This Cambridge-based role offers the opportunity to support Harvard’s mission and develop professional skills while working alongside a collaborative team.
As the Director of Accounting Operations at Scholar Rock, you will be at the forefront of our financial strategies, leading a dynamic team to enhance our accounting practices. Your expertise will drive the efficiency and accuracy of our financial operations, ensuring compliance with regulations and supporting our growth objectives. You will collaborate with …
Integrated Resources Inc. is seeking an experienced Clinical Operations Lead to join our dynamic team in Cambridge, Massachusetts. This pivotal role involves overseeing clinical trial operations, ensuring compliance with regulatory standards, and leading cross-functional teams to achieve project milestones. The ideal candidate will have a strong background in clinical research and a passion for advancing healthcare solutions.
Full-time|$160K/yr - $190K/yr|On-site|Cambridge, MA or New York City, NY
Iterative Health is at the forefront of healthcare technology and services, driving the evolution of clinical research to enhance patient outcomes. Our Site Network features over 70 premier clinical research sites across both the US and Europe, facilitating the rapid development of innovative gastrointestinal (GI) and hepatology therapies. We are dedicated to the success and expansion of our partner sites through the provision of tech-enabled services. By merging extensive clinical trial expertise with state-of-the-art AI technology, we empower research teams and study sponsors to broaden and accelerate access to transformative therapeutics for patients in need.About the RoleWe are on the lookout for a dynamic and driven Director of Operational Finance & Analytics to become an integral part of our expanding team. In this pivotal role, you will collaborate closely with executive leadership, finance, and operational teams to oversee the operational finance aspects of our growing network of research sites and enhance the company’s enterprise analytics capabilities, ensuring precision, consistency, and governance of critical metrics for a reliable single source of truth.Your contributions will be vital in constructing and scaling our Enterprise Data Warehouse (EDW) and executing Adaptive Insights, utilizing these essential systems to provide dependable reporting and forecasting that supports operational decision-making. This hands-on leadership position offers a unique opportunity to make a significant impact as the company evolves.
We are seeking a highly skilled and motivated Contract Clinical Operations Lead to join our dynamic team. In this pivotal role, you will oversee clinical trial operations, ensuring adherence to regulatory requirements and best practices. Your expertise will guide project management, resource allocation, and team coordination, driving the successful execution of clinical studies.
We are seeking an enthusiastic and detail-oriented Accounts Payable Operations Specialist to join our dynamic finance team. In this role, you will be responsible for managing the accounts payable process, ensuring timely and accurate payments to our vendors while maintaining strong relationships with them. You will play a crucial part in supporting the financial operations of our organization.
Join our dynamic team as a Compound Hub Operator at Artech Information Systems LLC in Cambridge, MA. This exciting entry-level position offers a unique opportunity to start your career in a fast-paced environment. As a Compound Hub Operator, you will be responsible for assisting in the operations of our compound hub, ensuring that processes run smoothly and efficiently.
Join Integrated Resources Inc. as a Clinical Operations Lead, where you will play a pivotal role in overseeing clinical trials and operations. You will be responsible for ensuring compliance, managing timelines, and leading a team of professionals dedicated to advancing healthcare solutions. Your expertise will help streamline processes and improve patient outcomes.
Nuvalent seeks an Associate Director of Clinical Operations to join the team in Cambridge, MA or work remotely. This leadership role guides the execution of clinical trials, ensuring every step aligns with regulatory standards and internal protocols. The position partners with cross-functional teams to develop and deliver on clinical strategies, overseeing studies from planning through closeout. What you will do Direct clinical trial operations for multiple concurrent studies Maintain compliance with all regulatory requirements and company procedures Work closely with colleagues across departments to create and implement clinical strategies Supervise all aspects of study management, from initiation to completion Oversee budgets, timelines, and resource planning for clinical programs Mentor and guide junior staff within clinical operations Requirements Significant experience in clinical operations and project management Background working in pharmaceutical or biotechnology organizations Demonstrated ability to manage budgets and timelines Experience mentoring or managing team members
About the Role Plants & Goodwin Inc. is hiring a Heavy Equipment Operator for construction projects in Cambridge. This position plays a key part in running heavy machinery to support ongoing site work. Main Responsibilities Operate equipment such as excavators, bulldozers, and cranes on active construction sites Follow all safety protocols and company procedures while on the job Support project teams by moving materials and preparing work areas as needed What Matters Here Commitment to safe equipment operation Attention to detail when following company standards Ability to work as part of a construction crew
Full-time|$220K/yr - $269.5K/yr|On-site|Cambridge, MA USA
Operating Principal – Summit PBU THE ROLE Join Summit, an innovative Business Unit within Flagship Pioneering, as an Operating Principal dedicated to launching and scaling our NewCos. In this pivotal role, you will oversee operations and strategy across multiple companies, spearhead corporate development efforts, and collaborate closely with scientific leaders to transform groundbreaking ideas into tangible outcomes. This position is perfectly suited for an entrepreneurial leader who excels in uncertain environments, effortlessly navigates between scientific and business realms, and is passionate about building organizations from the ground up to achieve significant growth. KEY RESPONSIBILITIES Lead the strategic and operational planning for one or more NewCos. Drive corporate development initiatives, including partnerships, financing, and strategic alliances, while engaging with the Board of Directors and other key stakeholders. Work directly with scientists and company leaders to align technical advancements with operational objectives. Recruit, mentor, and manage high-performing teams across various functions. Collaborate with Flagship's central teams (Finance, Talent, Legal/IP, HR) to implement best-in-class infrastructure for each company. Develop and execute operational and long-range plans, ensuring timely and budget-compliant achievement of milestones. Establish and maintain strong relationships with investors, partners, and key opinion leaders. PROFESSIONAL EXPERIENCE & QUALIFICATIONS Who you are: You are a dynamic operator and strategist who blends business leadership with scientific insight. You thrive in fast-paced, entrepreneurial settings and are driven by the mission of building organizations that leverage innovative science. Qualifications: 10+ years of experience in biotech, pharmaceuticals, or life sciences strategy/operations; prior management consulting experience is advantageous. Demonstrated success in strategic, operational, or corporate development roles, preferably in early-stage biotech. Strong scientific acumen; ability to rapidly comprehend novel scientific concepts and translate them into actionable plans. Proven track record in assembling and inspiring high-performing teams. Exceptional communication skills, capable of influencing and motivating investors, partners, and internal teams. Proficient problem solver; adept at bringing order to chaos and quickly iterating to find effective solutions. Entrepreneurial, resilient, and hands-on; able to adapt and execute with urgency, unafraid to roll up sleeves and get involved.
We are seeking a highly skilled and experienced Senior Clinical Operations Lead to join our dynamic team in Cambridge. As a pivotal member of our clinical operations team, you will play a critical role in overseeing the planning, execution, and management of clinical trials. Your expertise will ensure adherence to regulatory standards and best practices, while also fostering collaboration across multidisciplinary teams.Your responsibilities will include developing operational strategies, managing budgets, and ensuring timely project delivery. You will also be responsible for mentoring junior staff and facilitating training programs.
Join Harvard University as a Security Manager, reporting to the Director of Safety and Security. In this pivotal role, you will oversee and coordinate security operations, ensuring the safety of staff, visitors, collections, and physical assets at the Harvard Art Museums. As the front-line supervisor, you'll manage security staff during your shifts, applying your expertise with autonomy and sound judgment.Core Responsibilities:Oversee daily security operations at the Harvard Art Museums, managing staffing levels, post coverage, emergency responses, special events, and group visits.Supervise security personnel by scheduling shifts, monitoring performance, providing training, and addressing issues, with a professional approach focused on customer service.Act promptly in emergencies, including medical, fire, and life safety incidents, documenting incidents according to established protocols.Participate in the recruitment and training of new security personnel.Continuously enhance skills to effectively handle a variety of challenges.Optimize resource deployment for efficient operations.Plan daily workflows and support clerical duties, including payroll and timekeeping.Contribute to policy implementation and procedure development for the Security Department, making recommendations to the Director as needed.Assist in creating and applying new security measures to enhance visitor experiences.Utilize Microsoft Office to maintain records, compose communications, and manage statistical databases.Review video footage as needed for investigations and maintain security databases.Support event-related security activities, managing budgets and suggesting operational improvements.
Who is BlueRock?BlueRock Therapeutics LP is a pioneering clinical-stage company focused on advancing cell therapies to develop innovative treatments for individuals affected by neurological and ophthalmic diseases. Our flagship investigational cell therapies, bemdaneprocel (BRT-DA01) aimed at combating Parkinson’s disease and OpCT-001 targeting primary photoreceptor diseases, are at the forefront of clinical research. Established in 2016 through a collaboration between Versant Ventures and Leaps by Bayer, our culture is characterized by a relentless pursuit of excellence, a commitment to transforming medicine, and a strong sense of community and purpose.Our MissionWe leverage foundational scientific principles to facilitate the creation and differentiation of universal pluripotent stem cells into fully functional, authentic cellular therapies capable of addressing a diverse range of diseases. Our capabilities extend to engineering these cells to produce enzymes, antibodies, and various proteins for enhanced therapeutic outcomes.We are dedicated to fulfilling the promise of cellular and gene therapy, revolutionizing the landscape of cellular medicine, and providing new therapeutic options to millions of patients worldwide.We invite collaborative individuals who thrive in a vibrant, dynamic environment and are resolute in their commitment to advancing groundbreaking cellular therapies that profoundly impact patient lives.At BlueRock Therapeutics, we are excited about the ongoing advancements in cellular therapies that can significantly improve the lives of patients across various disease spectra.The Associate Director of Toxicology Operations will play a pivotal role, engaging with both internal and external stakeholders to manage nonclinical study plans that support BlueRock’s development pipeline. This position requires a Program Toxicologist who can effectively utilize their expertise in toxicology to propel the company’s initiatives forward, collaborating closely with program leads and other experts in the field.This role is based in Cambridge, Massachusetts, with a hybrid work arrangement (3 days in the office per week).
Who is BlueRock?BlueRock Therapeutics LP is an innovative clinical-stage biotechnology company specializing in cell therapy. Our mission is to develop groundbreaking medicines for individuals affected by neurological and ophthalmic disorders. Our lead investigational therapies, bemdaneprocel (BRT-DA01) for Parkinson’s disease and OpCT-001 for primary photoreceptor diseases, exemplify our commitment to transforming patient care. Founded in 2016 as a collaboration between Versant Ventures and Leaps by Bayer, our culture is characterized by resilience in the face of challenges, a sense of urgency in advancing medicine, integrity in our mission, and a strong community focus.What Are We Doing?At BlueRock, we leverage cutting-edge science to convert universal pluripotent stem cells into authentic, functional cells for allogeneic therapies targeting a wide range of diseases. Additionally, our engineering capabilities allow these cells to produce therapeutic proteins, enhancing treatment outcomes. Our dedication to cellular and gene therapy is unwavering, and we aim to deliver innovative solutions to millions of patients.We are looking for collaborative individuals who thrive in a vibrant and dynamic work environment, committed to advancing state-of-the-art cellular therapies that will improve patients' lives.The Associate Director of Vendor Management will play a pivotal role in managing and optimizing BlueRock’s essential Development vendor relationships, which are critical for the successful execution of our key clinical initiatives. This position is responsible for ensuring vendor performance, governance, and the overall health of relationships across key outsourced services such as CROs, central labs, imaging, and recruitment vendors.This role sits at the intersection of strategic leadership and operational execution, partnering closely with Clinical Operations, Finance, Procurement, and other functional leaders to ensure that vendors meet their contractual obligations, adapt to evolving program needs, and align with BlueRock’s overarching development strategy. The Associate Director will also be instrumental in establishing scalable, data-driven governance for vendors across Development.
Note: This is a vacation relief position, required to cover vacations and other absences.As a skilled Chiller Operator, you will expertly operate and service chilled water generation and distribution systems as well as associated equipment and components.You will be responsible for maintaining a thorough understanding of these systems, identifying and resolving issues in accordance with industry standards, codes, and university guidelines.Your duties will also include performing various trade skills and responsibilities related to the operation and maintenance of steam equipment, water distribution systems, and other related infrastructure.It is essential to maintain your work area, tools, and equipment according to university standards.You will work independently and collaboratively under the guidance of the Associate Manager or Working Foreman.Job-Specific Responsibilities:Operate the central chilled water plant under varying load conditions.Manage additional plant equipment including water treatment systems and compressed air systems.Collaborate with trades personnel and management to ensure continuous plant operations.Record and analyze critical plant readings essential for operational efficiency and billing (e.g., pressures, temperatures, flows).Complete daily logs, prepare necessary reports, and enter daily information into the computer system.Oversee the chemical treatment program and maintain accurate records.Conduct cleaning and maintenance of plant facilities and assigned boiler areas.Perform inspections and preventive maintenance on various equipment as directed.Operate and maintain various plant systems (including HVAC) to meet operational requirements.Work alongside utility mechanics and carry out other duties as directed.Maintain an organized and clean work environment with tools and equipment.Physical Requirements:Must be able to bend, reach, and maintain awkward postures for extended periods.Capable of lifting up to 75 pounds and assisting with equipment and tool transportation exceeding 300 pounds.Able to push and pull heavy loads as required.Must be comfortable working from ladders, in high places, confined spaces, and on scaffolding.Requires significant walking, climbing, bending, and stooping throughout the workday.
We are seeking a dedicated and knowledgeable Senior Associate in Operational Excellence & Compliance to join our dynamic team at Integrated Resources Inc. In this pivotal role, you will contribute to enhancing our operational processes and ensuring compliance with industry regulations. You will collaborate with cross-functional teams to identify opportunities for improvement and implement best practices that drive operational efficiency.
Full-time|$68K/yr - $78K/yr|On-site|Cambridge, MA USA
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.
Gopuff seeks full-time Operations Associates to join the Cambridge operations team. This position reports to a Site Leader and supports daily warehouse activities that keep the business moving. Role overview Operations Associates play a hands-on role in the warehouse, handling tasks such as picking and packing orders, receiving new inventory, and working closely with delivery riders. Each day brings a mix of responsibilities that help ensure customers receive their essentials quickly and reliably. What we look for Determination and a positive attitude Enjoyment in tackling challenges and solving problems Ability to work collaboratively with team members Creativity and willingness to try new approaches A genuine interest in snacks is a plus About Gopuff Gopuff delivers everyday essentials to customers at any hour, no matter the weather. The company values reliability, innovation, and a drive to reshape retail. Operations Associates are key to making this possible in Cambridge.
Overview: Gopuff is seeking dedicated full-time Operations Associates (OAs) to join our dynamic operations team in Cambridge. Reporting directly to a Site Leader, OAs are vital to our mission and embody qualities such as drive, resilience, positivity, and enthusiasm for overcoming challenges. Your role will encompass various warehouse duties including picking, packing, receiving products, and collaborating with our delivery riders.At Gopuff, we are committed to delivering everyday essentials to our customers—day or night, rain or shine. We are building a team of innovative thinkers, ambitious dreamers, and adventurous risk-takers who are eager to revolutionize the retail landscape at an unprecedented pace. And yes, a love for snacks is a bonus!
Harvard University’s Campus Services - Engineering & Utilities department seeks an Operations and Maintenance Analyst to join the team in Cambridge. This full-time position centers on reviewing and refining operational processes that help ensure reliable and efficient campus services. Key Responsibilities Examine current operations and maintenance procedures to understand existing workflows. Pinpoint opportunities for process improvement and greater efficiency. Contribute to efforts that maintain dependable campus services. Work Environment This Cambridge-based role offers the opportunity to support Harvard’s mission and develop professional skills while working alongside a collaborative team.