Senior Director, Global Head of Clinical Operations Olympus CorpSenior Director, Global Head of Clinical OperationsWestborough, MAThe Sr Director, Global Head of Clinical Operations reports directly to the Global Head of Clinical Research and collaborates closely with the MSA leadership team to provide strategic leadership and direction for the clinical operations team including the oversight of all aspects of clinical studies in support of clinical evidence generation strategies across global business unit portfolios. The individual is a critical member of Clinical Affairs leadership team and collaborates with cross-functional teams including internal and external business stakeholders within MSA, across the global business units, and within the broader Olympus organization, as appropriate.
Lead Ultrasound Tech-$15,000 Sign on Bonus Boston Medical CenterLead Ultrasound Tech-$15,000 Sign on BonusBoston, MA$34.38–$50 / hourLead Ultrasound Tech $15,000 Sign on Bonus 47717 725 Albany Street, Boston, Massachusetts Full Time Add to favorites View favorites POSITION SUMMARY: Under the general guidance of the Operations Manager, the Lead Tech provides administrative and technical leadership for the Antenatal Testing Unit (ATU). Position: Lead Ultrasound Tech Department: Antenatal Testing - M Schedule: Full Time ESSENTIAL RESPONSIBILITIES / DUTIES: Assists the Operations Manager in daily operations relating to the technical workings of the ATU and oversees the work of assigned technical staff and clinic flow coordinator.
NewPathology Tech Boston Children's HospitalPathology TechBoston, MA$26.62–$42.59 / hourPosition Summary/ Department Summary: Independently performs a variety of duties in the Surgical Cutting room, including processing of frozen tissue, dictation of gross descriptions, and surgical cutting of routine specimens. Rotates coverage in general Pathology by accessioning, preparing, documenting, and performing autopsies, storing specimens, and maintaining autopsy room in operating condition.
MRI Technologist, Weekends Brigham and Women's HospitalMRI Technologist, WeekendsChelsea, MA$42.86–$57.41 / hourThe framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. The scope of the MRI technologist includes preparing patients, positioning, setting imaging parameters, acquiring images, performing computer processing, and displaying images.
MRI Technologist, weekends Brigham and Women's HospitalMRI Technologist, weekendsChelsea, MA$31.98–$47.85 / hourThe framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. Demonstrates ability to prepare patient, positions for exam, set imaging parameters per protocol, perform computer processing, and displays images at request for both clinical and research patients.
MRI Technologist Weekends Brigham and Women's HospitalMRI Technologist WeekendsWaltham, MA$42.86–$57.41 / hourThe framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. The scope of the MRI technologist includes preparing patients, positioning, setting imaging parameters, acquiring images, performing computer processing, and displaying images.
NewAnalyst II, Quality Control Molecular Biology The Steely GroupAnalyst II, Quality Control Molecular BiologyWoburn, MAThe QC Analyst II will perform analytical methods including but not limited GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed to support in-process, drug substance and drug product release, stability to support AAV-based gene therapy programs. Routine work includes release and stability testing, critical reagent qualification, method validation and transfer, critical reagent qualification, analyzing data, and authoring technical documents.
Manager, Quality Control Consultant The Steely GroupManager, Quality Control ConsultantHybrid, Waltham, MAThe selected candidate will work collaboratively with Analytical Quality Control leaders to assess laboratory conformance with cGMPs, and with CMC Regulatory Affairs and Quality Assurance to ensure the translational accuracy and integrity of data incorporated into Module 3 sections of CTD regulatory submissions and written responses to regulatory authorities. Contribute to regulatory and technical documentation by reviewing QC data for accuracy, completeness, and traceability; verifying data transcription and data checks supporting regulatory submissions; and ensuring information is ready for inclusion in internal reports, APQRs, Module 3 submission-supporting documents, and responses to regulatory authorities.
Senior Manager, Corporate Quality - R&D Audits Sarepta Therapeutics IncSenior Manager, Corporate Quality - R&D AuditsBedford, MA$136,000–$170,000 / yearManager, Corporate Quality Audits, provides GxP oversight for the vendor management and audit program, with primary responsibility for GPV and GLP/GCLP vendor audits. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Vice Chair for Quality and Safety - Department of Obstetrics and Gynecology Boston Medical CenterVice Chair for Quality and Safety - Department of Obstetrics and GynecologyBrighton, MA$330,993–$380,906 / yearPresent at relevant department and hospital meetings, prepare consequent reports and policies, and craft and implement appropriate change, including, but not limited to: Regular case reviews in inpatient and outpatient obstetrics and gynecology in consultation with the System Chief and the perinatal safety nurse. Serve as a voice for Q&S issues and efforts at department and hospital meetings, including collaboration with the Quality and Patient Safety department, participation in internal QA presentations, communication of department and hospital Q&S efforts and priorities, and participation in graduate medical education priorities related to Q&S.
Quality Systems Specialist II - Training processes and Learning Management System (LMS) Integrated Resources, IncQuality Systems Specialist II - Training processes and Learning Management System (LMS)Mansfield, MassachusettsContractorQuality Systems Specialist II - Training Processes And Learning Management System (LMS)Implementation of the training process and Learning Management System (LMS)POSITION RESPONSIBILITIES: • Monitor and support consistent execution of Client's training process and quality training programs. • Consults with Client's leaders, process owner, and managers to ensure that the correct training is assigned to Client's employees.
Senior Engineer/Manager, Process Validation Stoke Therapeutics IncSenior Engineer/Manager, Process ValidationBedford, MA$140,000–$161,000 / yearCollaborate with internal and external partners to develop and define key product lifecycle documentation, including quality attribute and process risk assessments (FMEAs), process control strategy documents, continued process verification control plans, etc. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels.
Director, CMC Lead Stoke Therapeutics IncDirector, CMC LeadBedford, MA$225,000–$250,000 / yearSet the strategic direction for primary container closure and delivery device selection (e.g., pre-filled syringe), guiding cross-functional risk assessments on drug-device compatibility, stability, and long-term performance to protect product quality and patient safety. Position Purpose: The Stoke Therapeutics team is seeking an experienced and driven Director, CMC Lead to lead cross-functional teams that are accountable for chemistry, manufacturing, and controls (CMC) product lifecycle management.
Technical Sanitation Specialist (Hybrid/Regional Travel) HP HoodTechnical Sanitation Specialist (Hybrid/Regional Travel)Boston, MA$75,000–$93,000 / yearProvide technical leadership and guidance to Operations Quality, R&D, and manufacturing facilities in the areas of sanitation, pathogen/environmental control, integrated pest control, new equipment design, installation or construction and other food safety or quality initiatives related to sanitation processes. Manager, Strategic Sanitation Programs to establish long term strategic business plans, monitor corporate sanitation policies and help foster an environment of proactive sanitation across multiple departments and divisions.
Physician Assistant, Orthopedics Brigham and Women's HospitalPhysician Assistant, OrthopedicsNewton, MA$59.04–$83.59 / hourSchedules are finalized several months in advance, allowing providers to select from a wide variety of shifts, including weekend days, evenings, nights, and holidays. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success.
Senior/Staff System Test Engineer Flok Health LtdSenior/Staff System Test EngineerCambridge, MAYou'll collaborate closely with the rest of the engineering team (who will continue to also write tests) and all Flok employees (who will continue to help QA the product internally), but you'll be the go-to expert dedicated to test strategy and quality ownership. Our team has deep expertise across clinical, engineering and machine learning, has a track record of healthtech innovation, and is backed by top-tier VCs and multiple unicorn founder angels.
Post Market Surveillance Specialist Katalyst Healthcares & Life SciencesPost Market Surveillance SpecialistCambridge, MAServes as a liaison between Medical Affairs, Clinical Affairs, Research & Development, Services, and Complaint Handling to ensure Post Market Surveillance (PMS) and Risk Management (RM) processes are executed end-to-end (E2E). Minimum of 4-5 years' experience in Post Market Surveillance within FDA/EU-MDR regulated Medical Device environments with a focus on post-market surveillance plans/reports and post market risk assessment.
Post Market Surveillance (PMS) Specialist Katalyst Healthcares & Life SciencesPost Market Surveillance (PMS) SpecialistCambridge, MAServes as a liaison between Medical Affairs, Clinical Affairs, Research & Development, Services, and Complaint Handling to ensure Post Market Surveillance (PMS) and Risk Management (RM) processes are executed end-to-end (E2E). Minimum of 4-5 years' experience in Post Market Surveillance within FDA/EU-MDR regulated Medical Device environments with a focus on post-market surveillance plans/reports and post market risk assessment.
NP or PA Manager, Nuclear Cardiology- MGH Brigham and Women's HospitalNP or PA Manager, Nuclear Cardiology- MGHBoston, MA$130,249.60–$190,278.40 / yearNo Licenses and Credentials Physician Assistant [State License] - Generic - HR Only required Experience Experience as a licensed Physician Assistant 5-7 years required Knowledge, Skills and Abilities - Strong clinical knowledge as a Physician Assistant. Provides direct management to typically a small to medium-sized team of advanced practice providers or other allied health professionals while continuing to spend the majority of time providing direct patient care as a Physician Assistant.
Senior Engineer, Test Automation Care AccessSenior Engineer, Test AutomationBoston, MARemote$130,000–$180,000 / yearWith programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. You will bring deep technical expertise in Playwright-based automation and hands-on experience with GxP validation, while also exploring how AI-augmented testing approaches can scale coverage and reduce manual toil.