Medical Device Toxicologist III
$78.3kBoston Scientific
Additional Location(s): US-MN-Arden Hills; US-MA-Marlborough Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. About The Role The Medical Device Toxicologist III at Boston Scientific provides technical support for toxicology and biocompatibility processes to meet global business objectives. This position contributes to the biological evaluation of medical device products, including toxicological risk assessments based on data from extractables and leachables studies, in support of new product development, sustaining activities and global regulatory submissions. The role applies established standards, procedures and risk-based approaches to help ensure patient safety and product quality while enabling timely product development and regulatory decisions. Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. Work model, sponsorship, relocation At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time. Your Responsibilities Will Include Support biocompatibility and toxicology processes initiated by department management and help ensure related information and data are accurate, reliable and aligned with Global Preclinical objectives and Quality Management System requirements. Demonstrate a primary commitment to patient safety and product quality. Author biocompatibility and chemical characterization test plans, biocompatibility assessments and reports, and assess test data and reports as assigned to support business objectives. Author toxicological risk assessments as assigned to support divisional objectives, applying established procedures, precedents and scientific judgment. Provide informal guidance to new or less-experienced team members on established biocompatibility and chemical characterization processes, as appropriate. Maintain communication with internal customers on biocompatibility and toxicology topics and support the resolution of straightforward to moderately complex issues related to biological evaluation, chemical characterization and toxicological risk assessment. Support biocompatibility, chemistry and toxicology testing strategies for assigned investigational and device development programs during technology and product development programs (TDP/PDP). Apply working knowledge of regulatory requirements and internal procedures to support medical device submissions for assigned projects and divisions, with guidance on complex or unprecedented issues. Participate, as assigned, in biocompatibility training for device development teams based on applicable standards, procedures and regulatory requirements. Serve as a resource for factual biocompatibility and toxicology information for medical devices and pharmaceutical materials, which may include materials of animal origin, color additives, chemical exposure assessments and other chemical toxicities. Apply established procedures, techniques, concepts and approaches to assigned biocompatibility and toxicology programs; identify issues and escalated complex or unprecedented matters as appropriate. Qualifications Required qualifications Bachelor's degree in toxicology or a closely related field, such as biology, chemistry, biochemistry or biomedical engineering. Minimum of 3 years' experience in a related field. Knowledge of the biological evaluation of medical devices and/or drug-device combination products. Preferred Qualifications Master's degree in toxicology or a closely related field, such as biology, chemistry, biochemistry or biomedical engineering. Candidates with a master's degree and a minimum of 1 year's related experience will be considered. Doctoral degree in toxicology or a related field, such as biology, chemistry, biochemistry or biomedical engineering. Solid knowledge and practical application of toxicology principles and best practices. Working knowledge of risk assessment methodologies, including the toxicological evaluation of medical device materials. Working knowledge of regulatory standards and global regulatory requirements for medical devices and combination products. Experience supporting GLP and non-GLP studies. Excellent written and verbal communication skills. Results-oriented and detail-oriented approach. Ability to manage multiple assignments and priorities while meeting project timelines. Ability to work effectively in a dynamic environment with a moderate level of guidance, independently on assigned work and collaboratively as part of a team. Requisition ID: 633532 Minimum Salary: $ 78300 Maximum Salary: $ 148800 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). For MA positions It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at follow us onLinkedIn. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination. Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law. #J-18808-Ljbffr Boston Scientific
- ...Boston Scientific is seeking an AI Platform System Administrator III to operate, secure and support enterprise AI platform... ...related technologies.Experience in health care, life sciences, medical devices or a large global enterprise.Requisition ID: 633651Minimum Salary...Medical deviceHourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- ...ability to travel up to 40%, including internationallyProven track record of successful commercialization and product launches in medical device industryGlobal downstream experience (i.e. product management, sales engagement and campaign)Ability to work effectively in a...Medical deviceHourly payWork at officeLocal areaRelocation packageShift work3 days per week
- Acara Solutions is recruiting for a Manufacturing Team Member in Hudson, MA. This temporary role involves basic assembly and inspection work following written procedures to meet quality and production standards. The position supports a wire rack and coatings workflow, with...Medical deviceTemporary work
- ...seeking a Design Assurance Engineer to join a leading global technology company. The role focuses on Class II electro-mechanical medical devices across the full development lifecycle, from design and risk assessment to verification, validation, and regulatory submissions....Medical device
- ...Technical seeks a Mechanical Engineer in Marlborough, MA for a hybrid contract role with remote onsite balance. You will support medical device development, design verification, and quality documentation within a fast-paced engineering environment. Responsibilities...Medical deviceContract workRemote work
- ...role focuses on design controls, risk management, verification/validation, and regulatory compliance across electro-mechanical medical devices. The ideal candidate has 3-5 years of Class II medical device experience, with exposure to FDA/CE submissions and external testing...Medical deviceFull time
- ...Marlborough, MA is seeking a design engineering professional to lead development and validation of Class II electro-mechanical medical devices. You will design controls, support risk management, and collaborate with regulatory teams. This exempt role requires a Bachelor...Medical device
- Hologic, Inc. in Marlborough, MA is seeking a Senior Product Development Engineer to lead new product development from concept to production, applying customer-centric design and strong technical judgment. You will mentor junior engineers, manage subsystems, run technical...Medical device
- ...a Design Assurance Engineer to join its team in Marlborough, MA. This is a great opportunity for an engineer with 3-5 years of medical device experience who wants to take on meaningful work across the full product development lifecycle. You’ll help develop and improve...Medical deviceFull time
- ...documentation for improving the manufacturing of new and existing devices. Support R&D team in developing supplier quality plans,... ...disposable kit products for a regulated industry (e.g. medical device, class II and/or class III). Experience in verification activities related to...Medical deviceContract work
- ...frequent domestic travel. Qualifications Bachelor's Degree. Minimum of 10 years of professional experience within the healthcare/medical device industry. Minimum of 5 years of downstream marketing experience + 5 years of sales experience. Direct experience supporting or...Medical deviceContract work
$140k - $160k
...communication across US Sales Channels.Required Qualifications:Bachelor’s DegreeMinimum of 8 years of experience within healthcare/medical device industry in a commercial role (i.e downstream marketing or sales)Understanding of: Healthcare contracting structures (tiers,...Medical deviceFull timeContract workRelocation package- ...out of various locations in the US, Canada and IndiaQualifications--Additional InformationWe are looking candidate who has some medical device, bio/pharm or similar environment/ background, experience or knowledge. SummaryType: ContractFunction: Health Care...Medical device
- ...supporting our rapidly growing active implantable device portfolio. This role will be responsible... ...filings for new and modified Class III products Provides technical reviews of... ...Regulatory Affairs experience in the medical industry Prior experience with 510(k) submissions...Medical deviceHourly payWork at officeLocal areaRelocationShift work3 days per week
- Hologic, Inc. is seeking a Diagnostic Specialist to drive sales of the APTIMA product line, ThinPrep Pap Test and adjunctive testing within a defined territory. You will develop sales strategies, forecast performance and maintain strong relationships with clinicians and...Medical device
- A medical device company is seeking an Anaplan Model Builder in Marlborough, MA. This hybrid position involves optimizing Anaplan solutions for Sales Compensation, supporting existing models, and collaborating across departments. Candidates should have significant experience...Medical device
- ...IPG Medical Corporation Job OpportunityIPG Medical Corporation is focused on developing next-generation medical products based on its... ...that improve life.Our mission is to develop innovative medical device laser solutions that make the world a better place. To accomplish...Medical device
- Integer Holdings is a global organization providing innovative technologies and manufacturing to Medical Device OEMs to enhance lives, with a focused culture on EHSS excellence. This EHSS Engineer role supports systems and drives programs to maintain a safe workplace and...Medical device
- ...Job Description Job Description D&R Products, a medical device manufacturing company in Hudson, MA, is looking for dependable Assembly / Machine Operators to join our production team. This is a hands-on manufacturing position that involves operating production...Medical deviceFull time
- ...of the Sr. Program Manager will be to work directly with a cross-functional team who is responsible for the development of new medical devices and systems in the Surgical Division to:Lead small and large NPD projects from start to finish, coordinate Design History File...Medical device
- ...of Global Toxicology and Biocompatibility to lead the development and oversight of biocompatibility and toxicology programs for medical devices. You will guide testing strategies, ensure regulatory readiness, and align activities with corporate goals to support safe,...Medical device
$140k - $175k
...security-related issues across networked systems, applications, and devices* Collaborate with cross-functional teams to improve product... ...are preferred* Experience in regulated industries, healthcare, medical devices, or compliance-focused environments is a plusJob...Medical device- ...of senior-level facilities or site operations experience , preferably within the pharmaceutical, biotech, life sciences, or medical device industry , with experience supporting laboratory environments. Key Responsibilities Lead day-to-day property management...Medical deviceWork at office
- ...team members, contribute to 5S practices, manage Kanban levels, and help identify waste while ensuring safety and quality in a medical device manufacturing environment. The role emphasizes flexibility, cross-training, and continuous improvement through Lean methods and...Medical device
$129.5k - $203.5k
...producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around... ...and organization skillsPreferred ExperienceCardiovascular or medical device market experienceGlobal / cross-cultural...Medical deviceRemote work- Candela Medical is seeking a Director of Regulatory Affairs based in Marlborough, Massachusetts. This senior position is responsible for... ...and executing global regulatory strategies for medical devices, managing complex regulatory challenges, and ensuring compliance...Medical device
- Boston Scientific seeks a Line Maintenance Technician in Marlboro, MA. The role involves working with project teams, R&D technicians, engineers, and scientists on equipment release and preventative maintenance. The position is onsite five days a week and requires coordinating...Medical device
- ...Requirements:Bachelors degree in Engineering or related discipline.Experience in verification validation testing| preferably in medical devices or other regulated industries.Familiarity with automated test systems and documentation best practices.Strong analytical|...Medical device
- Are you passionate about ensuring the safety and reliability of life-saving medical devices? At Hologic, we are seeking a Quality Assurance Engineer - Product Quality to play a critical role in managing product holds, stop ships, corrections, and field actions. In this...Medical device
- ...reporting, UDI governance, and regulatory database management, ensuring compliant and scalable processes while supporting a growing medical device portfolio. The incumbent directs the regulatory team, collaborates with R&D, Quality, Clinical and Manufacturing, and...Medical device
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Medical Device Toxicologist III. Be the first to apply!

