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Medical Device Toxicologist I Jobs

Medical Device Tester Jobs
By Peritus Inc At St Paul, MN, United States

Experience in verification/testing is preferred.

medical device domain or related industry

Medical Device Quality Systems Coordinator
By Akkodis At Mount Prospect, IL, United States
Medical Device Quality Systems Coordinator job responsibilities include:
• Three plus years experience in the Medical Device Industry.
• Solid experience working in a Class I and Class II Medical Device environment.
• Extensive knowledge of medical device regulations/standards including 21 CFR 820 (QSR) and ISO - 13485:2016.
Pay/Salary Range: $40.00 and $45.00 per hour.
• MasterControl Maintenance - New employee set-up, Employee terminations, Password resets, Administrative back-up.
Medical Device Tester Jobs
By Abbott At Irving, TX, United States
Some laboratory or diagnostics experience desired.
Ability to demonstrate competency of computer skills.
B.S. in Computer Science or similar engineering discipline including Software Engineering, Biomedical Engineering, or Laboratory Science desired.
Title- Medical Device Tester I
Timings- 8am to 5 pm
Specialist I, Regulatory Affairs - Medical Device
By Werfen At , San Diego, 92121 $75,000 - $85,000 a year
Assist in interactions regarding regulatory affairs with all functional areas of the company as required including senior management.
Must possess a strong willingness to comply with regulations and procedures and provide transparency to management regarding all work related issues.
Experience and knowledge regarding global premarket clearance activities preferred.
Experience and knowledge regarding global post market activities preferred.
Responsibilities may include pre-market and/or post-market as defined by the company.
Assist in tracking standards, regulations and all applicable requirements.
Medical Specialist I Jobs
By Regeneron At , Tarrytown
Experience with in-servicing and training office staff, nurses and office managers
Demonstrate advanced clinically based selling skills
Develop strategy and execute tactics within key accounts in the Dermatology therapeutic area to generate product utilization.
Results oriented with a proven track record of success with product launches
A Typical Day Might Look Like This:
This Position Might be for You if:
Medical Device Repair Technician I
By STERIS At , Fort Lauderdale, 33330
What skills, experience, and abilities will make you successful in this role?
Generally, successful candidates and employes have the following general skills, experience, and
Minimum 1 year of overall work experience
Comfortable with and have general computer use skills.
Experience in a similar role or environment using similar tools/equipment.
Excellent healthcare, dental, and vision benefits with low
Specialist I, Regulatory Affairs - Medical Device
By Werfen At , San Diego, 92121, Ca $75,000 - $85,000 a year
Assist in interactions regarding regulatory affairs with all functional areas of the company as required including senior management.
Must possess a strong willingness to comply with regulations and procedures and provide transparency to management regarding all work related issues.
Experience and knowledge regarding global premarket clearance activities preferred.
Experience and knowledge regarding global post market activities preferred.
Responsibilities may include pre-market and/or post-market as defined by the company.
Assist in tracking standards, regulations and all applicable requirements.
Remote: Qa Medical Device Contractor (233511)
By Black Diamond Networks At United States
Knowledge of ISO 9001 and ISO 13485
General knowledge of QA and RA compliance for Class I Med Devices
Experience mentoring younger staff is a plus (+)
8-10 Years working in FDA regulated Medical Device Industry
Working with Salesforce and D365 is preferred
Qa Medical Device Contractor (233511)
By Black Diamond Networks At United States
Knowledge of ISO 9001 and ISO 13485
General knowledge of QA and RA compliance for Class I Med Devices
Experience mentoring younger staff is a plus (+)
8-10 Years working in FDA regulated Medical Device Industry
Working with Salesforce and D365 is preferred
Degree: Not needed but preferred
Project Coordinator (Medical Device)
By Select Source International At United States
• 4 years of administrative/project support experience
5+ years of work experience as a project coordinator/administrative assistant
• Capable of working on multiple projects in a deadline driven environment - demonstrated skill under pressure
• Excellent written and verbal communication, and interpersonal skills
• Strong prioritization and organizational skills
• High School Diploma or equivalent
Nonclinical Toxicologist - Remote
By Proclinical Staffing At Boston, MA, United States
Maintain study files and records using electronic document management systems (eDMS).
Work with internal contract managers to implement study contracts.
Be familiar with requirements of regulatory authorities for toxicology studies to support IND and NDA (e.g., ICH and OECD guidelines).
Minimum of 5 years of experience in conducting/monitoring nonclinical toxicology studies
Single point of Toxicology contact between pharma and CROs.
Provide Toxicological expertise to support the development of nonclinical toxicology study protocols and data interpretation.
Toxicologist Jobs
By Battelle At Columbus, OH, United States
Effective verbal and written communication skills including correct grammar, spelling, and punctuation. Prior presentation experience.
Observes appropriate safety and study requirements by reading, understanding, and following SOP’s, GLP regulations, and study protocols.
Manages studies within time and budget constraints.
Oversees the building of new capabilities to bring in new technologies and services.
Demonstrated competency in regulated environment including prior experience working in a GLP or similarly regulated environment.
Advance your education: Tuition assistance is available to pursue higher education.
Medical Device Warehouse Associate: Starting Rate $24.50/Hr.
By Stryker At , Sacramento, 95834, Ca $24.50 an hour
2+ years of experience required; Warehouse/Inventory Control experience in a demanding and fast-paced environment -preferred
Compile and inspect incoming/outgoing KIT(s) for compliance with specifications and usage
Examine and inspect stock items for wear or defects, reporting any damage to supervisors
Confer with distribution, sales, shipping, warehouse, or common carrier personnel in order to expedite or trace deliveries
Set up and organize the warehouse for incoming and outgoing surgery shipments
Clean and maintain supplies, tools, equipment, and storage areas in order to ensure compliance with safety regulations
Medical Device Warehouse Associate: Starting Rate $22.25/Hr.
By Stryker At , Pittsburgh, Pa $22.25 an hour
2+ years of experience required
Compile and inspect incoming/outgoing kits for compliance with specifications and usage
Examine and inspect stock items for wear or defects, reporting any damage to supervisors
Confer with distribution, sales, shipping, warehouse, or common carrier personnel in order to expedite or trace deliveries
Set up and organize the warehouse for incoming and outgoing surgery shipments
Clean and maintain supplies, tools, equipment, and storage areas in order to ensure compliance with safety regulations
Clinical Medical Device Guru
By Greenlight Guru At United States
Accurately manage and forecast churn, renewals, and upsells
Experience from the clinical trials area of the MedTech or life science industry.
Great team player who can work well within the team and collaborate cross-functionally, especially in a remote environment
Ability to wear multiple hats and gracefully juggle varying customer needs and responsibilities
Assist in addressing and resolving customer support requests reported through Greenlight Guru Clinical’s help desk and other channels
Assist with other customer success tasks that come up from time to time, such as study and dashboard set up.
Medical Device Quality Assurance
By Pfizer At , San Jose, Ca $113,900 - $189,700 a year
Experience in post-market change management of medical devices and combination products
Prior experience in management of quality technical resources
Prior experience in management of external vendors and suppliers
Act as the medical device quality support for the lifecycle management site /sustaining engineering and ensuring QMS execution and continuous improvement.
Provide Quality Assurance support and direction to project teams accountable for IVD change projects, complaint investigations and change management.
Ensure risk management activities are developed in accordance with ISO 14971 and local procedures.
Intern, Medical Device Jobs
By Curia At , Lebanon, 08833, Nj
Interpret and communicate test results to senior management
Participate in routine testing, method develop and validation as per ISO and ASTM and/or client requirements
Develop a working knowledge of the test methods being used to analyze samples
Good written, math and verbal skills, highly organized and decision-making ability focused around details
Operate test equipment for integrity and functional testing
Ability to work independently, take initiative and handle multiple tasks within defined timelines
Forensic Toxicologist Iii, Medical Examiner
By Tarrant County, TX At , , Tx $5,559 - $6,115 a month
Tarrant County employees enjoy superior health, retirement, and insurance benefits &
Four (4) full-time years of work experience in a forensic toxicology laboratory or other applicable laboratory experience
Physical Demands and Work Environment & Other Requirements
Performs accessioning, analysis, and evaluation of evidence utilizing standardized and industry acceptable techniques.
Analyzes evidence (biological or other) for the presence of drugs, alcohol, and other analytes and reports results.
Performs routine preventive maintenance on equipment and quality control procedures.
Medical Device Assembler Jobs
By Reincarnate GP At United States

On time arrival to work, regular attendance without excessive absenteeism, and working a full 8 hour or longer work period

Medical Device Sanitization Manager
By TriMedx At , Columbia, Sc
Knowledge of the healthcare industry, including an understanding or experience with hospital medical equipment preferred.
Comprehensive benefits package including medical, dental, vision, 401K
Bachelor’s degree preferred or equivalent work experience.
At least 3 years of customer excellence experience.
Efficient computer skills and the willingness to learn new computer applications to complete required job functions
Valid driver's license required; variable travel requirements depending on primary site that may require use of personal vehicle

Are you looking for a challenging and rewarding career in medical device toxicology? We are looking for a highly motivated and experienced Medical Device Toxicologist to join our team. You will be responsible for evaluating the safety and efficacy of medical devices, assessing potential risks, and developing strategies to mitigate those risks. You will also be responsible for developing and implementing testing protocols and providing technical support to regulatory agencies. If you are passionate about medical device safety and have the skills and experience to make a difference, this could be the perfect opportunity for you!

Overview Medical Device Toxicologist I is responsible for assessing the safety of medical devices and their components. They must be knowledgeable in the principles of toxicology and have a thorough understanding of the regulatory requirements for medical device safety. They must be able to interpret and evaluate toxicological data and provide recommendations to ensure the safety of medical devices. Detailed Job Description The Medical Device Toxicologist I is responsible for assessing the safety of medical devices and their components. This includes evaluating the safety of materials used in the manufacture of medical devices, assessing the potential for adverse effects from exposure to medical devices, and providing recommendations to ensure the safety of medical devices. The Medical Device Toxicologist I must be knowledgeable in the principles of toxicology and have a thorough understanding of the regulatory requirements for medical device safety. They must be able to interpret and evaluate toxicological data and provide recommendations to ensure the safety of medical devices. Job Skills Required
• Knowledge of the principles of toxicology
• Knowledge of medical device safety regulations
• Ability to interpret and evaluate toxicological data
• Ability to provide recommendations to ensure the safety of medical devices
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
Job Qualifications
• Bachelor’s degree in toxicology, biology, chemistry, or a related field
• At least two years of experience in a toxicology-related field
• Knowledge of medical device safety regulations
• Ability to interpret and evaluate toxicological data
• Excellent communication and interpersonal skills
Job Knowledge
• Knowledge of the principles of toxicology
• Knowledge of medical device safety regulations
• Ability to interpret and evaluate toxicological data
• Knowledge of medical device manufacturing processes
Job Experience
• At least two years of experience in a toxicology-related field
• Experience in medical device safety assessment
• Experience in medical device manufacturing processes
Job Responsibilities
• Assess the safety of medical devices and their components
• Evaluate the safety of materials used in the manufacture of medical devices
• Assess the potential for adverse effects from exposure to medical devices
• Interpret and evaluate toxicological data
• Provide recommendations to ensure the safety of medical devices
• Monitor and report on the safety of medical devices
• Maintain knowledge of medical device safety regulations