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Join Serán BioScience, a dynamic and growing company, as a Quality Assurance Engineer. This is an exciting opportunity to contribute to our expanding team, where you will play a crucial role in ensuring the quality and compliance of our Commercial Manufacturing Facility. As a QA Engineer, you will collaborate with cross-functional teams to review and approve qualification and validation processes related to our facilities, utilities, equipment, processes, cleaning, and computerized systems.
Your expertise will be vital in facilitating effective communication between internal and external teams, ensuring alignment on quality strategies, and addressing any deficiencies while fostering positive relationships. Candidates should possess a solid understanding of current regulations and guidelines, including but not limited to 21 CFR Parts 11, 210, and 211, EudraLex Volume 4, Annex 15, and GAMP 5.
Join Serán BioScience, a dynamic and growing company, as a Quality Assurance Engineer. This is an exciting opportunity to contribute to our expanding team, where you will play a crucial role in ensuring the quality and compliance of our Commercial Manufacturing Facility. As a QA Engineer, you will collaborate with cross-functional teams to review and approve…
Role Overview Serán BioScience seeks a Director of Quality Engineering & Computer System Assurance (CSA) to lead validation, qualification, and computerized systems assurance efforts. This position is based in Bend, Oregon and supports GMP manufacturing, laboratory, and quality systems for both clinical and commercial operations. Main Responsibilities Develop and maintain a risk-based framework for validation and CSA across facilities, utilities, equipment, analytical methods, processes, and computerized systems. Ensure all validation and data integrity activities meet FDA, EU, and international regulatory standards, including cGMP and GAMP guidance. Oversee the full lifecycle of validation for systems and processes, ensuring ongoing compliance and readiness for inspection. Collaborate with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to support compliant, reliable manufacturing. Represent Serán BioScience during regulatory inspections, client audits, and internal quality reviews. Drive continuous improvement in validation lifecycle management, computerized system assurance, and data governance. Collaboration and Leadership This Director role works cross-functionally to ensure validated systems and processes support the company's clinical and commercial product goals. The position acts as a key Quality leader and organizational representative in regulatory and client-facing settings.
Role overview The Director of Commercial Quality Assurance at Seran Bio provides leadership for quality assurance activities in Bend, Oregon. This position ensures that commercial products meet established quality standards and supports the ongoing development of quality management systems. Close collaboration with teams across the company is central to maintaining and improving these systems. What you will do Lead quality assurance programs focused on commercial products Work with cross-functional teams to advance quality initiatives Implement and sustain quality management systems Identify and drive improvements in quality processes Ensure compliance with all relevant regulatory requirements Foster a strong culture of quality throughout Seran Bio
Join Serán BioScience as a Quality Assurance Associate and contribute to our commitment to regulatory compliance in the manufacturing of oral solid dosage drug products. In this pivotal role, you will support the Quality Assurance department's daily activities, ensuring adherence to GMP regulations and internal SOPs throughout the clinical manufacturing process. Key responsibilities include reviewing and approving production records, analytical data, and QA documentation. You will also conduct risk analyses, manage investigations, and participate in audits and inspections. A strong background in GMP Pharmaceutical Manufacturing is essential, and compensation will be commensurate with experience. This position operates on an alternative manufacturing schedule from Monday to Thursday, starting at 2:00 PM and concluding at 1:00 AM. Familiarity with Serán's manufacturing capabilities and the ability to make informed independent decisions in line with Company policies and risk mitigation strategies are crucial for success in this role.
Turner Townsend is seeking a Quality Assurance Project Manager with a focus on electrical systems for data center construction projects in Bend. This position centers on upholding rigorous quality standards and supporting project delivery from an electrical perspective. Role overview This role involves leading quality assurance activities for electrical installations within data center construction. The Project Manager will monitor compliance with industry standards and client requirements, ensuring that all electrical components are installed and tested to specification. Key responsibilities Oversee and coordinate quality control procedures for electrical systems Track project milestones related to electrical work Work closely with stakeholders to address quality concerns and maintain project alignment Implement safety and service standards throughout the construction process Requirements Experience in quality assurance or project management within electrical or data center construction Strong understanding of industry standards for electrical systems Ability to coordinate with multiple stakeholders and oversee project milestones
Role overview Serán BioScience, LLC is hiring a Vice President of Quality to lead clinical and commercial quality teams at its Bend, Oregon location. This executive role shapes quality operations within a growing Contract Development and Manufacturing Organization (CDMO), guiding the launch and growth of a new facility for commercial manufacturing of advanced medicines. What you will do Develop and execute the company’s Quality Strategy across all stages of clinical and commercial manufacturing. Manage the Quality Management System (QMS) to meet GMP, GXP, FDA, EMA, and other international regulatory standards. Promote a culture of accountability, continuous improvement, and proactive risk management throughout Serán BioScience. Collaborate with executive leadership to embed quality practices from early clinical development through commercial operations. Uphold Serán’s reputation as a reliable partner by maintaining high standards for manufacturing quality and scalability. About Serán BioScience Serán BioScience, LLC is a CDMO offering contract development and manufacturing services for innovative medicines. The company is expanding with a new facility in Bend, Oregon, supporting both clinical and commercial supply.
Veeva Systems is a purpose-driven organization and leader in industry cloud solutions, dedicated to accelerating the delivery of therapies to patients by life sciences companies. As one of the fastest-growing SaaS companies ever, we achieved over $2 billion in revenue in our last fiscal year, with significant growth opportunities on the horizon.At Veeva, our core values guide us: Do the Right Thing, Customer Success, Employee Success, and Speed. We are not just another public company; we made history in 2021 by becoming a public benefit corporation (PBC), committed to balancing the interests of our customers, employees, society, and investors.Join us in transforming the life sciences industry, and making a meaningful impact on our customers, employees, and communities.The RoleWe are seeking a proactive and technically adept Senior Engineering Manager in Test to spearhead our test automation and quality engineering teams for Vault CRM and associated products. This role demands a manager who remains deeply involved in the technical aspects, actively participating in automation design and troubleshooting, while leading by example.You will be responsible for harmonizing leadership responsibilities with hands-on technical engagement, collaborating closely with engineers to conceptualize, assess, and enhance automation solutions while promoting quality initiatives across teams.
About Serán BioScience Serán BioScience provides customized formulation, process development, and clinical manufacturing services for pharmaceutical clients. Our work supports a broad range of projects and partners across the industry. Role Overview: Quality Control Lab Technician The Quality Control Department seeks a Laboratory Technician to support ongoing sample testing. This role plays a key part in maintaining compliance with good manufacturing practices (GMP) and supporting customer satisfaction. Lab Technicians work closely with team members to ensure all testing meets our quality standards. What You Will Do Perform sample testing and documentation according to GMP guidelines Support daily lab operations and maintain accurate records Work collaboratively with colleagues to meet departmental goals Communicate proactively to address issues and share updates What We Look For Attention to detail in all laboratory tasks Ability to work well in a busy setting Strong teamwork and clear communication skills Self-discipline and reliability Lab experience is welcome, but not required Location This position is based in Bend, Oregon.
We are seeking a dedicated and proactive Manufacturing Engineer to join our dynamic team at The Wonderful Company. In this role, you will play a crucial part in improving our manufacturing processes to enhance efficiency and product quality. Your expertise will help us innovate and implement advanced manufacturing techniques.This position offers an exciting opportunity to work in a collaborative environment where your ideas and contributions will be valued. You will work closely with cross-functional teams to analyze production data, troubleshoot issues, and optimize workflows.
Project Engineer Join Western Partitions, Inc. (WPI), a leading and highly respected contractor specializing in interior and exterior construction across the United States. We are dedicated to delivering exceptional contracting services in drywall, prefabrication, metal studs, acoustical systems, wall panels, fireproofing, firestopping, stucco, claddings, painting, windows, doors/frames/hardware, and more. Since our establishment in 1972, we have built a legacy of award-winning construction that prioritizes integrity, safety, and efficiency. Our commitment to our clients is reflected in the high percentage of repeat business we receive. Our service-oriented, fast-track approach, along with meticulous attention to detail, has earned us a stellar reputation in the industry. We strive every day to uphold the trust and confidence of our customers. Our history is defined by our commitment to our employees and the quality of work we produce. A significant source of our pride comes from completing each job with excellence. Our team is motivated to get it right the first time, and our clients choose WPI because of our emphasis on communication, trust, and respect. Job Description The Project Engineer will work closely with the Project Manager to set up, manage, and close out projects at either the Regional office or job site. This role is crucial for achieving project objectives through effective planning, scheduling, and execution of project activities from inception to completion. This is an entry-level construction management position. Adhere to all WPI policies, procedures, and corporate safety programs. Actively engage in safety protocols and measures on assigned projects. Review contract terms, scope of work, and special provisions; ensure project team members are informed. Assist with procurement and buyout processes for materials, subcontractor services, and engineering quotes. Prepare Requests for Information (RFIs), submittals, and shop drawings. Support and visit assigned job sites while participating in necessary job meetings. Evaluate change requests and update project budgets accordingly. Compile, review, and report weekly production metrics. Discuss weekly job cost reports with the project Foreman and team. Prepare billing documentation and approve invoices for payment. Monitor project progress and financial expenditures to ensure timely and budget-compliant completion. Assist in the implementation of project schedules. Coordinate warranties, operation and maintenance manuals, and project closeout documentation.
Seran Bio seeks a Process Engineer based in Bend, Oregon. The position centers on refining production processes to strengthen efficiency and maintain high quality throughout manufacturing. Key responsibilities Collaborate with cross-functional teams to spot and carry out process improvements Contribute to projects aimed at raising operational efficiency and product quality Assist in making sure manufacturing systems meet company standards Location This role is located in Bend, Oregon.
Join Serán BioScience as a Senior Validation Engineer and contribute to the establishment of a cutting-edge commercial manufacturing facility. This pivotal role involves collaborating with a dynamic cross-functional team to spearhead commissioning and qualification (CQ) projects for equipment and critical utilities, facilitate tech transfers from clinical to commercial manufacturing, and oversee validation processes for production, cleaning, and computerized systems for non-sterile pharmaceutical products. The ideal candidate will possess extensive experience, ideally exceeding 8 years, in Oral Solid Dosage forms, coupled with a passion for team leadership. However, we encourage applicants with a range of experiences to apply. As a key member of the Commercial Steering Committee, you will take charge of planning and executing CQ and validation initiatives. A comprehensive understanding of manufacturing processes, applicable regulations, and effective communication strategies is essential for success in this role. You will play a crucial role in liaising with both internal and external teams to align strategies, mitigate risks, and foster strong working relationships.
Join Speechify, a leading innovator in the text-to-speech technology space, as a Software Engineer specializing in platform development. You will play a critical role in enhancing our platform's performance, scalability, and user experience. Collaborate with cross-functional teams to design, develop, and maintain high-quality software solutions that empower our users.
Join our dynamic team at The Wonderful Company as a Process Engineer specializing in Chemical Operations, where you will play a pivotal role in optimizing our production processes. This is an exciting opportunity to utilize your engineering skills to improve efficiency, enhance safety, and contribute to our commitment to sustainability.
Seranbio seeks an Engineering Associate to join the team in Bend, Oregon. This position plays a key part in supporting projects that drive the company’s mission forward. The focus is on developing and applying technical solutions that improve how daily operations run. Responsibilities Apply technical knowledge to support current projects Assist in creating and implementing solutions that enhance operational processes Location This position is based onsite in Bend, Oregon.
Join The Wonderful Company as a Product Development Engineer where you will play a crucial role in bringing innovative products to market. This position is perfect for those looking to leverage their engineering skills to drive product success from concept to commercialization.
Join Veeva, a trailblazer in the industry cloud and one of the fastest-growing enterprise SaaS firms, dedicated to expediting the delivery of life-saving therapies to patients across the globe. As a public benefit corporation (PBC), we are committed to harmonizing the needs of our customers, employees, society, and investors, presenting a unique opportunity to create solutions that significantly improve global health.The Opportunity: As a Principal Software Engineer at Veeva, you will play a key role in the design and development of robust, scalable enterprise applications that enable our customers to operate efficiently and safely. Your leadership will be crucial in guiding our technological advancements. You will mentor junior engineers, steer essential technical decisions, and consistently produce high-quality code that drives our technology forward.Thrive in Our Work Anywhere Environment: We empower you to work from wherever you thrive—be it from home or in the office across Canada or the US—ensuring seamless collaboration within your team's time zone.Join Veeva and be an integral part of transforming the life sciences industry, making a genuine impact on global health.
Veeva Systems is a pioneering, mission-driven organization at the forefront of industry cloud solutions, dedicated to accelerating the delivery of therapies to patients in the life sciences sector. Recognized as one of the fastest-growing SaaS companies, we achieved over $2 billion in revenue last fiscal year, with extensive growth opportunities on the horizon.At Veeva, our core values are rooted in integrity: Do the Right Thing, Customer Success, Employee Success, and Speed. We made a historic leap in 2021 by becoming a public benefit corporation (PBC), committed to balancing our responsibilities to customers, employees, society, and investors.As a Work Anywhere company, we offer the flexibility to work from home or in the office, empowering you to excel in your preferred environment.Join us in transforming the life sciences industry and making a meaningful impact on our customers, employees, and communities.The RoleAs a Principal Full Stack Engineer, you will leverage your extensive experience to create scalable cloud software that accelerates the innovation and delivery of essential treatments and medicines globally. This senior position grants you the autonomy to influence project direction, advise product leadership, and mentor emerging software engineers.
Serán Bioscience is actively seeking a highly skilled Senior Process Engineer specializing in spray drying technology to contribute to the commercial scaling of innovative drug products. In this pivotal role, you will be the technical steward of commercial spray drying systems, ensuring optimal, compliant, and efficient operations across various unit processes including solution preparation, spray drying, and secondary drying. This position uniquely blends hands-on expertise with long-term system management, focusing on continuous enhancement, equipment reliability, and product excellence. As the appointed system owner, you will be responsible for the generation and updating of equipment documentation packages, facilitating regulatory and client audits, and ensuring compliance with current Good Manufacturing Practices (cGMP). You will maintain a robust, data-driven understanding of equipment performance, analyze trends to preemptively address issues, and drive initiatives that improve reliability, yield, and product quality. This role necessitates close collaboration with Maintenance, Quality, Validation, and Manufacturing teams to synchronize spare parts strategies, preventative maintenance, calibration schedules, and the implementation of clean-in-place systems. Within a Contract Development and Manufacturing Organization (CDMO) framework, you will also work alongside clients and internal teams to support technology transfers, scale-up initiatives, and lifecycle management of spray drying processes.
Veeva Systems is a mission-driven pioneer in the industry cloud space, dedicated to assisting life sciences companies in delivering therapies to patients in a more efficient manner. As one of the fastest-growing SaaS companies in history, we achieved over $2 billion in revenue in our most recent fiscal year, with tremendous growth opportunities on the horizon.Our core values at Veeva include: Do the Right Thing, Customer Success, Employee Success, and Speed. We are not just another public company; we made history in 2021 by becoming a public benefit corporation (PBC), which means we are legally committed to balancing the interests of our customers, employees, society, and investors.As a Work Anywhere organization, we encourage flexible work arrangements, allowing you to operate from home or in the office, fostering an environment where you can thrive.Join us in transforming the life sciences industry and making a positive impact on our customers, employees, and communities.The RoleAre you enthusiastic about exploring new technologies and understanding their functionalities? Do you want to collaborate with a dynamic team to elevate our products? We are seeking a skilled and innovative Senior Performance Engineer to concentrate on the scalability and performance of our products while establishing meaningful benchmarks that reflect customer use cases.At Veeva, we rigorously evaluate each software release to ensure it meets our customers' demands. As a Senior Performance Engineer, you will play a critical role in our product success. Collaborating with developers, you will test and optimize Veeva's applications before their release, and monitor and resolve performance issues in production. You will work closely with product management, gaining direct insight into the usage patterns we aim to address. This role is technical and hands-on, ideal for someone skilled in gathering and analyzing performance data to identify the root causes of performance bottlenecks.
Join Serán BioScience, a dynamic and growing company, as a Quality Assurance Engineer. This is an exciting opportunity to contribute to our expanding team, where you will play a crucial role in ensuring the quality and compliance of our Commercial Manufacturing Facility. As a QA Engineer, you will collaborate with cross-functional teams to review and approve…
Role Overview Serán BioScience seeks a Director of Quality Engineering & Computer System Assurance (CSA) to lead validation, qualification, and computerized systems assurance efforts. This position is based in Bend, Oregon and supports GMP manufacturing, laboratory, and quality systems for both clinical and commercial operations. Main Responsibilities Develop and maintain a risk-based framework for validation and CSA across facilities, utilities, equipment, analytical methods, processes, and computerized systems. Ensure all validation and data integrity activities meet FDA, EU, and international regulatory standards, including cGMP and GAMP guidance. Oversee the full lifecycle of validation for systems and processes, ensuring ongoing compliance and readiness for inspection. Collaborate with Engineering, Manufacturing, Quality Control, IT, Regulatory Affairs, and Technical Operations to support compliant, reliable manufacturing. Represent Serán BioScience during regulatory inspections, client audits, and internal quality reviews. Drive continuous improvement in validation lifecycle management, computerized system assurance, and data governance. Collaboration and Leadership This Director role works cross-functionally to ensure validated systems and processes support the company's clinical and commercial product goals. The position acts as a key Quality leader and organizational representative in regulatory and client-facing settings.
Role overview The Director of Commercial Quality Assurance at Seran Bio provides leadership for quality assurance activities in Bend, Oregon. This position ensures that commercial products meet established quality standards and supports the ongoing development of quality management systems. Close collaboration with teams across the company is central to maintaining and improving these systems. What you will do Lead quality assurance programs focused on commercial products Work with cross-functional teams to advance quality initiatives Implement and sustain quality management systems Identify and drive improvements in quality processes Ensure compliance with all relevant regulatory requirements Foster a strong culture of quality throughout Seran Bio
Join Serán BioScience as a Quality Assurance Associate and contribute to our commitment to regulatory compliance in the manufacturing of oral solid dosage drug products. In this pivotal role, you will support the Quality Assurance department's daily activities, ensuring adherence to GMP regulations and internal SOPs throughout the clinical manufacturing process. Key responsibilities include reviewing and approving production records, analytical data, and QA documentation. You will also conduct risk analyses, manage investigations, and participate in audits and inspections. A strong background in GMP Pharmaceutical Manufacturing is essential, and compensation will be commensurate with experience. This position operates on an alternative manufacturing schedule from Monday to Thursday, starting at 2:00 PM and concluding at 1:00 AM. Familiarity with Serán's manufacturing capabilities and the ability to make informed independent decisions in line with Company policies and risk mitigation strategies are crucial for success in this role.
Turner Townsend is seeking a Quality Assurance Project Manager with a focus on electrical systems for data center construction projects in Bend. This position centers on upholding rigorous quality standards and supporting project delivery from an electrical perspective. Role overview This role involves leading quality assurance activities for electrical installations within data center construction. The Project Manager will monitor compliance with industry standards and client requirements, ensuring that all electrical components are installed and tested to specification. Key responsibilities Oversee and coordinate quality control procedures for electrical systems Track project milestones related to electrical work Work closely with stakeholders to address quality concerns and maintain project alignment Implement safety and service standards throughout the construction process Requirements Experience in quality assurance or project management within electrical or data center construction Strong understanding of industry standards for electrical systems Ability to coordinate with multiple stakeholders and oversee project milestones
Role overview Serán BioScience, LLC is hiring a Vice President of Quality to lead clinical and commercial quality teams at its Bend, Oregon location. This executive role shapes quality operations within a growing Contract Development and Manufacturing Organization (CDMO), guiding the launch and growth of a new facility for commercial manufacturing of advanced medicines. What you will do Develop and execute the company’s Quality Strategy across all stages of clinical and commercial manufacturing. Manage the Quality Management System (QMS) to meet GMP, GXP, FDA, EMA, and other international regulatory standards. Promote a culture of accountability, continuous improvement, and proactive risk management throughout Serán BioScience. Collaborate with executive leadership to embed quality practices from early clinical development through commercial operations. Uphold Serán’s reputation as a reliable partner by maintaining high standards for manufacturing quality and scalability. About Serán BioScience Serán BioScience, LLC is a CDMO offering contract development and manufacturing services for innovative medicines. The company is expanding with a new facility in Bend, Oregon, supporting both clinical and commercial supply.
Veeva Systems is a purpose-driven organization and leader in industry cloud solutions, dedicated to accelerating the delivery of therapies to patients by life sciences companies. As one of the fastest-growing SaaS companies ever, we achieved over $2 billion in revenue in our last fiscal year, with significant growth opportunities on the horizon.At Veeva, our core values guide us: Do the Right Thing, Customer Success, Employee Success, and Speed. We are not just another public company; we made history in 2021 by becoming a public benefit corporation (PBC), committed to balancing the interests of our customers, employees, society, and investors.Join us in transforming the life sciences industry, and making a meaningful impact on our customers, employees, and communities.The RoleWe are seeking a proactive and technically adept Senior Engineering Manager in Test to spearhead our test automation and quality engineering teams for Vault CRM and associated products. This role demands a manager who remains deeply involved in the technical aspects, actively participating in automation design and troubleshooting, while leading by example.You will be responsible for harmonizing leadership responsibilities with hands-on technical engagement, collaborating closely with engineers to conceptualize, assess, and enhance automation solutions while promoting quality initiatives across teams.
About Serán BioScience Serán BioScience provides customized formulation, process development, and clinical manufacturing services for pharmaceutical clients. Our work supports a broad range of projects and partners across the industry. Role Overview: Quality Control Lab Technician The Quality Control Department seeks a Laboratory Technician to support ongoing sample testing. This role plays a key part in maintaining compliance with good manufacturing practices (GMP) and supporting customer satisfaction. Lab Technicians work closely with team members to ensure all testing meets our quality standards. What You Will Do Perform sample testing and documentation according to GMP guidelines Support daily lab operations and maintain accurate records Work collaboratively with colleagues to meet departmental goals Communicate proactively to address issues and share updates What We Look For Attention to detail in all laboratory tasks Ability to work well in a busy setting Strong teamwork and clear communication skills Self-discipline and reliability Lab experience is welcome, but not required Location This position is based in Bend, Oregon.
We are seeking a dedicated and proactive Manufacturing Engineer to join our dynamic team at The Wonderful Company. In this role, you will play a crucial part in improving our manufacturing processes to enhance efficiency and product quality. Your expertise will help us innovate and implement advanced manufacturing techniques.This position offers an exciting opportunity to work in a collaborative environment where your ideas and contributions will be valued. You will work closely with cross-functional teams to analyze production data, troubleshoot issues, and optimize workflows.
Project Engineer Join Western Partitions, Inc. (WPI), a leading and highly respected contractor specializing in interior and exterior construction across the United States. We are dedicated to delivering exceptional contracting services in drywall, prefabrication, metal studs, acoustical systems, wall panels, fireproofing, firestopping, stucco, claddings, painting, windows, doors/frames/hardware, and more. Since our establishment in 1972, we have built a legacy of award-winning construction that prioritizes integrity, safety, and efficiency. Our commitment to our clients is reflected in the high percentage of repeat business we receive. Our service-oriented, fast-track approach, along with meticulous attention to detail, has earned us a stellar reputation in the industry. We strive every day to uphold the trust and confidence of our customers. Our history is defined by our commitment to our employees and the quality of work we produce. A significant source of our pride comes from completing each job with excellence. Our team is motivated to get it right the first time, and our clients choose WPI because of our emphasis on communication, trust, and respect. Job Description The Project Engineer will work closely with the Project Manager to set up, manage, and close out projects at either the Regional office or job site. This role is crucial for achieving project objectives through effective planning, scheduling, and execution of project activities from inception to completion. This is an entry-level construction management position. Adhere to all WPI policies, procedures, and corporate safety programs. Actively engage in safety protocols and measures on assigned projects. Review contract terms, scope of work, and special provisions; ensure project team members are informed. Assist with procurement and buyout processes for materials, subcontractor services, and engineering quotes. Prepare Requests for Information (RFIs), submittals, and shop drawings. Support and visit assigned job sites while participating in necessary job meetings. Evaluate change requests and update project budgets accordingly. Compile, review, and report weekly production metrics. Discuss weekly job cost reports with the project Foreman and team. Prepare billing documentation and approve invoices for payment. Monitor project progress and financial expenditures to ensure timely and budget-compliant completion. Assist in the implementation of project schedules. Coordinate warranties, operation and maintenance manuals, and project closeout documentation.
Seran Bio seeks a Process Engineer based in Bend, Oregon. The position centers on refining production processes to strengthen efficiency and maintain high quality throughout manufacturing. Key responsibilities Collaborate with cross-functional teams to spot and carry out process improvements Contribute to projects aimed at raising operational efficiency and product quality Assist in making sure manufacturing systems meet company standards Location This role is located in Bend, Oregon.
Join Serán BioScience as a Senior Validation Engineer and contribute to the establishment of a cutting-edge commercial manufacturing facility. This pivotal role involves collaborating with a dynamic cross-functional team to spearhead commissioning and qualification (CQ) projects for equipment and critical utilities, facilitate tech transfers from clinical to commercial manufacturing, and oversee validation processes for production, cleaning, and computerized systems for non-sterile pharmaceutical products. The ideal candidate will possess extensive experience, ideally exceeding 8 years, in Oral Solid Dosage forms, coupled with a passion for team leadership. However, we encourage applicants with a range of experiences to apply. As a key member of the Commercial Steering Committee, you will take charge of planning and executing CQ and validation initiatives. A comprehensive understanding of manufacturing processes, applicable regulations, and effective communication strategies is essential for success in this role. You will play a crucial role in liaising with both internal and external teams to align strategies, mitigate risks, and foster strong working relationships.
Join Speechify, a leading innovator in the text-to-speech technology space, as a Software Engineer specializing in platform development. You will play a critical role in enhancing our platform's performance, scalability, and user experience. Collaborate with cross-functional teams to design, develop, and maintain high-quality software solutions that empower our users.
Join our dynamic team at The Wonderful Company as a Process Engineer specializing in Chemical Operations, where you will play a pivotal role in optimizing our production processes. This is an exciting opportunity to utilize your engineering skills to improve efficiency, enhance safety, and contribute to our commitment to sustainability.
Seranbio seeks an Engineering Associate to join the team in Bend, Oregon. This position plays a key part in supporting projects that drive the company’s mission forward. The focus is on developing and applying technical solutions that improve how daily operations run. Responsibilities Apply technical knowledge to support current projects Assist in creating and implementing solutions that enhance operational processes Location This position is based onsite in Bend, Oregon.
Join The Wonderful Company as a Product Development Engineer where you will play a crucial role in bringing innovative products to market. This position is perfect for those looking to leverage their engineering skills to drive product success from concept to commercialization.
Join Veeva, a trailblazer in the industry cloud and one of the fastest-growing enterprise SaaS firms, dedicated to expediting the delivery of life-saving therapies to patients across the globe. As a public benefit corporation (PBC), we are committed to harmonizing the needs of our customers, employees, society, and investors, presenting a unique opportunity to create solutions that significantly improve global health.The Opportunity: As a Principal Software Engineer at Veeva, you will play a key role in the design and development of robust, scalable enterprise applications that enable our customers to operate efficiently and safely. Your leadership will be crucial in guiding our technological advancements. You will mentor junior engineers, steer essential technical decisions, and consistently produce high-quality code that drives our technology forward.Thrive in Our Work Anywhere Environment: We empower you to work from wherever you thrive—be it from home or in the office across Canada or the US—ensuring seamless collaboration within your team's time zone.Join Veeva and be an integral part of transforming the life sciences industry, making a genuine impact on global health.
Veeva Systems is a pioneering, mission-driven organization at the forefront of industry cloud solutions, dedicated to accelerating the delivery of therapies to patients in the life sciences sector. Recognized as one of the fastest-growing SaaS companies, we achieved over $2 billion in revenue last fiscal year, with extensive growth opportunities on the horizon.At Veeva, our core values are rooted in integrity: Do the Right Thing, Customer Success, Employee Success, and Speed. We made a historic leap in 2021 by becoming a public benefit corporation (PBC), committed to balancing our responsibilities to customers, employees, society, and investors.As a Work Anywhere company, we offer the flexibility to work from home or in the office, empowering you to excel in your preferred environment.Join us in transforming the life sciences industry and making a meaningful impact on our customers, employees, and communities.The RoleAs a Principal Full Stack Engineer, you will leverage your extensive experience to create scalable cloud software that accelerates the innovation and delivery of essential treatments and medicines globally. This senior position grants you the autonomy to influence project direction, advise product leadership, and mentor emerging software engineers.
Serán Bioscience is actively seeking a highly skilled Senior Process Engineer specializing in spray drying technology to contribute to the commercial scaling of innovative drug products. In this pivotal role, you will be the technical steward of commercial spray drying systems, ensuring optimal, compliant, and efficient operations across various unit processes including solution preparation, spray drying, and secondary drying. This position uniquely blends hands-on expertise with long-term system management, focusing on continuous enhancement, equipment reliability, and product excellence. As the appointed system owner, you will be responsible for the generation and updating of equipment documentation packages, facilitating regulatory and client audits, and ensuring compliance with current Good Manufacturing Practices (cGMP). You will maintain a robust, data-driven understanding of equipment performance, analyze trends to preemptively address issues, and drive initiatives that improve reliability, yield, and product quality. This role necessitates close collaboration with Maintenance, Quality, Validation, and Manufacturing teams to synchronize spare parts strategies, preventative maintenance, calibration schedules, and the implementation of clean-in-place systems. Within a Contract Development and Manufacturing Organization (CDMO) framework, you will also work alongside clients and internal teams to support technology transfers, scale-up initiatives, and lifecycle management of spray drying processes.
Veeva Systems is a mission-driven pioneer in the industry cloud space, dedicated to assisting life sciences companies in delivering therapies to patients in a more efficient manner. As one of the fastest-growing SaaS companies in history, we achieved over $2 billion in revenue in our most recent fiscal year, with tremendous growth opportunities on the horizon.Our core values at Veeva include: Do the Right Thing, Customer Success, Employee Success, and Speed. We are not just another public company; we made history in 2021 by becoming a public benefit corporation (PBC), which means we are legally committed to balancing the interests of our customers, employees, society, and investors.As a Work Anywhere organization, we encourage flexible work arrangements, allowing you to operate from home or in the office, fostering an environment where you can thrive.Join us in transforming the life sciences industry and making a positive impact on our customers, employees, and communities.The RoleAre you enthusiastic about exploring new technologies and understanding their functionalities? Do you want to collaborate with a dynamic team to elevate our products? We are seeking a skilled and innovative Senior Performance Engineer to concentrate on the scalability and performance of our products while establishing meaningful benchmarks that reflect customer use cases.At Veeva, we rigorously evaluate each software release to ensure it meets our customers' demands. As a Senior Performance Engineer, you will play a critical role in our product success. Collaborating with developers, you will test and optimize Veeva's applications before their release, and monitor and resolve performance issues in production. You will work closely with product management, gaining direct insight into the usage patterns we aim to address. This role is technical and hands-on, ideal for someone skilled in gathering and analyzing performance data to identify the root causes of performance bottlenecks.
