68 matching jobs for “Robotics Product Specialist”

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Johnson & Johnson

Regulatory Affairs Specialist

Markham, Canada

Full time
Regular

Pay posted by employer$61,000–$98,900 CAD

… trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their journey to wellness. Learn more at …

Added Oct 15, 2026

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Johnson & Johnson

Senior Regulatory Affairs Specialist

Warsaw, Indiana, United States of America +2 locations

Full time
Regular

Pay posted by employer$79,000–$127,650

Added Oct 15, 2026

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Johnson & Johnson

Senior Hospital Operations Specialist

West Chester, Pennsylvania, United States +2 locations

Pay posted by employer$79,000–$127,650

Added Oct 18, 2026

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Johnson & Johnson

The Regulatory Affairs Specialist II

Warsaw, Indiana, United States of America +4 locations

Full time
Regular

Pay posted by employer$76,000–$121,900

Added Oct 15, 2026

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Caterpillar

Autonomy Engineering Specialist - MineStar Onboard

Irving, Texas, United States

Pay posted by employer$128,470–$208,770

… to deliver autonomy, productivity and safety capabilities at customer sites. The Autonomy Engineering Specialist sits between Site Solutions, Site Systems and L6 Solutions, breaking site-level system designs down into …

Added Oct 27, 2026

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Johnson & Johnson

Trauma Hospital Operations Specialist

West Chester, Pennsylvania, United States +1 location

Full time
Regular

Pay posted by employer$65,000–$104,650

Added Oct 15, 2026

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KLA

Export Control Classification Specialist

JPN-Japan-Remote-KLA

Full time
Regular

… consists of Service Sales and Marketing, Spares Supply Chain management, Field Operations, Engineering, Product Training, and Technical Support. The KLA Services organization partners with our field teams and customers …

Added Oct 15, 2026

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Caterpillar

Senior Autonomy Systems Engineering Specialist

Irving, Texas, United States +1 location

Pay posted by employer$128,470–$208,770

… the new era of construction autonomy at Caterpillar. Job Summary As a Senior Autonomy Systems Engineering Specialist on the Surface Loading Autonomy team, you will be an integral part of the Caterpillar team developing the …

Added Oct 27, 2026

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GE Aerospace

Regional Lead Customs Specialist

Singapore

Full time
Regular

… across the Asia Pacific region. From automating processes to leveraging smart factory technologies, robotics, and additive manufacturing, GE Aerospace is shaping the future of aviation. Responsible for more than 60% …

Added Oct 27, 2026

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Booz Allen Hamilton

Property Accountability Specialist and Site Lead

Hertford, NC

Pay posted by employer$69,300–$158,000

Property Accountability Specialist and Site Lead The Opportunity: As a Logistics Management Analyst and Site Lead, you’ll bring your …

Added Oct 30, 2026

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Baker Hughes

Manufacturing Specialist (M/F/D)

IT-SO-TALAMONA-VIA ROMA, 32

Full time

… Provide technical support to production teams to troubleshoot issues, reduce downtime, and ensure product quality. Support continuous improvement initiatives and promote best practices across manufacturing …

Added Oct 28, 2026

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Thermo Fisher Scientific

Technical Sales Specialist for Lab Automation

Gangnam-gu, Korea, Republic of

… making sure our food is safe or helping find cures for cancer. Job Description As a Technical Sales Specialist for Lab Automation Solutions at Thermo Fisher Scientific, you will play a critical role in driving business …

Added Oct 16, 2026

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Johnson & Johnson

Lead Specialist, Spine and Sports Education

Raynham, Massachusetts, United States of America

Full time
Regular

Pay posted by employer$94,000–$151,800

Added Oct 15, 2026

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Johnson & Johnson

Sales Specialist Joint Reconstruction| Johnson & Johnson MedTech| Orthopaedics| Nottinghamshire

Nottinghamshire, England, United Kingdom

Full time
Regular

… time and subject to any necessary consultation processes. DePuy Synthes is seeking a highly motivated Sales Specialist — Nottinghamshire & surrounds, Hip & Knee Reconstruction portfolio Overview Lead a nationally important …

Added Oct 15, 2026

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Johnson & Johnson

Regulatory Affairs Specialist I – Spine

Raynham, Massachusetts, United States of America

Pay posted by employer$64,000–$102,350

Added Oct 20, 2026

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Baker Hughes

Manufacturing Experienced Professional - Manuf Eng Specialist (d/f/m)

IT-SO-TALAMONA-VIA ROMA, 32

Full time

Added Oct 27, 2026

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Johnson & Johnson

Specialist, Field Education & Sales Enablement (Spine) – Core & Enabling Technologies

Raynham, Massachusetts, United States of America

Full time
Regular

Pay posted by employer$94,000–$149,500

DePuy Synthes is recruiting for a Specialist, Field Education and Sales Enablement (Spine) – Core and Enabling Technologies in Raynham, MA, USA. The …

Added Oct 16, 2026

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Johnson & Johnson

Regional Clinical Sales Specialist - Scottsdale, AZ - Johnson & Johnson MedTech - Orthopaedics

Scottsdale, Arizona, United States

Full time
Regular

We are searching for the best talent for Regional Clinical Sales Specialist to support clients in Scottsdale, AZ territory. About Orthopaedics Fueled by innovation at the intersection …

Added Oct 16, 2026

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Johnson & Johnson

Clinical Sales Specialist, Sports – Houston, TX – Johnson & Johnson MedTech - Orthopaedics

Houston, Texas, United States

Full time
Regular

We are searching for the best talent for a Clinical Sales Specialist to support the Houston, TX territory. About Orthopaedics Fueled by innovation at the intersection of …

Added Oct 15, 2026

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Johnson & Johnson

Clinical Sales Specialist (Chattanooga, TN) – Johnson & Johnson MedTech, Orthopaedics - Spine

Chattanooga, Tennessee, United States

Full time
Regular

We are searching for the best talent for Clinical Sales Specialist to support clients in Chattanooga, TN territory. About Orthopaedics Fueled by innovation at the …

Added Oct 15, 2026

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Johnson & Johnson

Regulatory Affairs Specialist

Markham, Canada

Full time
Regular

Pay posted by employer$61,000–$98,900 CAD

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Required Skills · employer excerpt

Analytical Reasoning, Business Writing, Collaborating, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Environment, Regulatory Reporting,…
The expected base pay range for this position is $61,000.00 to $98,900.00 CAD.
Under current guidelines, this position is eligible for a discretionary performance bonus.
AI Usage Disclosure
The Company uses Artificial Intelligence in its assessment of applicants.

4 more in the full description below.

About this opportunity

Original employer description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

Professional

All Job Posting Locations:

Markham, Ontario, Canada

Job Description:

About Orthopaedics

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems.

Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

We are searching for the best talent for the Regulatory Affairs Specialist in

Markham, Ontario, Canada.

You will be responsible for:

Develop and execute Canadian Regulatory strategies for complex Class III and Class IV medical devices, including combination products, to achieve and exceed business objectives.

Manage all Regulatory aspects of the product lifecycle from pre-market to post-marketing phase including reviewing and approving promotional material in alignment with corporate and Health Canada requirements.

Provide Regulatory consultation for business partners and provide expert Regulatory guidance to all internal stakeholders.

Establish and maintain strong relationships with Health Canada and business partners, driving collaboration on submission strategies, Regulatory pathways, submission status updates, recalls, and special access processes.

Maintain and continuously improve the Quality Management System (QMS) at DePuy Synthes in accordance with Health Canada regulations and corporate requirements, covering critical Regulatory and quality processes (i.e. submission management, renewal, special access, distribution, CAPA, change controls, document/records management) to enhance efficiency, compliance and overall performance.

Participate and support preparation and execution of internal and external audits, including Health Canada and MDSAP inspections.

Maintain awareness of new industry issues, trends and changes in regulation and policy and effectively communicate issues to key internal and external business partners. Coordinate comments on proposed regulations and policies.

Qualifications / Requirements:

University/Bachelor’s or equivalent degree in a Life Science, Engineering, or Physical Science is required.

Completion of post-graduate program in Quality/Regulatory Affairs is preferred.

3 - 5 years of experience in Medical Device and/or Pharmaceutical / Biologics Regulatory Affairs is preferred.

Sound knowledge of Food and Drugs Act and Regulations and relevant policies and guidelines is required.

Experience in managing regulatory submission activities is required.

Excellent skills in verbal and written communication are required.

Ability to develop and maintain strong working relationships with business partners and key stakeholders is required.

Demonstrated leadership skills is required.

Proven experience in successfully collaborating across functions and delivering business results is required.

Strong documentation skills and technical writing capability is required.

Detail-oriented and ability to align with business objectives is required.

Experience in supporting health authority and or Notified Body inspections is an asset.

Proven ability to execute Regulatory submission strategies that align with business objectives and ensure compliance with applicable regulations is required.

Analytical and problem-solving skills, with the ability to effectively prioritize, organize, and manage multiple tasks is required.

Skills in managing change and implementation of new processes are preferred.

Experience in Quality system experience and strategic thinking in emerging and changing requirements preferred is an asset.

Experience in ISO 13485, or other Quality Systems Experience is an asset.

Experience in Canadian Regulatory Affairs for medical devices and combination products preferred.

Required Skills:

Preferred Skills:

Analytical Reasoning, Business Writing, Collaborating, Communication, Legal Support, Problem Solving, Product Licensing, Public Policies, Regulatory Affairs Management, Regulatory Compliance, Regulatory Environment, Regulatory Reporting, Risk Assessments, Strategic Thinking

The expected base pay range for this position is $61,000.00 to $98,900.00 CAD.

Under current guidelines, this position is eligible for a discretionary performance bonus.

AI Usage Disclosure

The Company uses Artificial Intelligence in its assessment of applicants.

Vacancy Disclosure

This job posting is for an existing position.

Accessibility for Ontarians with Disabilities Act

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Required Skills:

Preferred Skills:

Why this result? · Employer labels

Keywords also found in description

Full time
Regular
Regulatory Affairs Group

Location reference: GeoNames (CC BY 4.0), normalized by Referizz.