Quality Assurance Regulatory Affairs Specialist
2 weeks ago
Job Title: Quality Assurance Regulatory Affairs Specialist
At Fluidigm, we are seeking a Quality Assurance Regulatory Affairs Specialist to support the development and implementation of quality and regulatory strategies for our products.
Key Responsibilities:
- Maintain technical documentation files in compliance with international requirements.
- Oversee the company REACH and Safety Data Sheet program.
- Approval and release of quality records, device history records, batch records master labels, and device master records.
- Support and administration of risk assessment review process and implementation of changes to risk management process as needed.
- Liaison with domestic and international customers and vendors to ensure compliance with standards and execution of corrective actions.
- Development of controlled documents and procedures pertinent to quality assurance activities and functions.
- Assists with customer complaints/CAPA system.
- Supports new product development, risk analysis, and launch processes, and manage QA participation on new production development.
Requirements:
- Bachelor's degree required, life science/engineering.
- Regulatory Affairs/Quality Management RAC certificate is preferred.
- Experience with ISO 13485, ISO 9001, required.
- Knowledge of and experience with the following standards: IEC 60601-1, ISO 13485, ISO 14971, IEC 62366, IEC 62304, CE-IVDR, and 21 CFR 820.
- Knowledge with REACH, RoHS, WEEE, CE mark, UKCA directives, and Safety Data Sheet compliance.
- ASQ Certification preferred but not required (such as CQA, CQE, CMQ/OE).
- 1-2 years of industry experience preferred.
- ISO 13485 Internal Auditor certificate a plus.
- Salesforce Experience a plus.
- Basic knowledge of Excel.
- Fast learner, self-starter, accountable, reliable.
- Ability to successfully work in a dynamic environment.
- Able to work under pressure and tight timelines.
- Problem-solving attitude.
- Cross-functional perspective and coordination.
About Fluidigm:
Fluidigm is a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health.
Why Join Us:
At Fluidigm, we are building a positive culture where our people can do the best work of their careers, informed, and influenced by our core behaviors:
- Keep customers front and center in all of our work.
- Be accountable and deliver on commitments.
- Drive continuous improvement.
- Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment.
Equal Opportunity Employer:
Fluidigm is committed to providing an inclusive and barrier-free recruitment process to applicants with accessibility needs in accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act (AODA). If you require an accommodation during this process, please inform Fluidigm of your requirements. We are an equal opportunity employer.
-
Quality Assurance Regulatory Affairs Specialist
2 weeks ago
Markham, Ontario, Canada fluidigm Full timeJob SummaryWe are seeking a Quality Assurance Regulatory Affairs Specialist to support the quality and regulatory activities of our products. The successful candidate will be responsible for maintaining and ensuring that our quality system meets requirements for medical devices and international directives.Key ResponsibilitiesMaintain Technical Documentation...
-
Quality Assurance Regulatory Affairs Specialist
2 weeks ago
Markham, Ontario, Canada fluidigm Full timeJob Title: Quality Assurance Regulatory Affairs AssociateJob Summary:We are seeking a highly motivated and detail-oriented Quality Assurance Regulatory Affairs Associate to join our team. The successful candidate will be responsible for maintaining and ensuring that our company's quality system meets requirements for medical devices and international...
-
Markham, Ontario, Canada fluidigm Full timeJob Title: Quality Assurance and Regulatory Affairs AssociateJob Summary:We are seeking a highly motivated and detail-oriented Quality Assurance and Regulatory Affairs Associate to join our team at Standard BioTools. The successful candidate will be responsible for maintaining and ensuring that our company quality system meets requirements for medical...
-
Quality Assurance/Regulatory Affairs Associate
1 month ago
Markham, Ontario, Canada fluidigm Full timeJob Title: Quality Assurance/Regulatory Affairs AssociateJob Summary:We are seeking a highly motivated and detail-oriented Quality Assurance/Regulatory Affairs Associate to join our team. The successful candidate will be responsible for maintaining and ensuring that our quality system meets requirements for medical devices, and International Directives. This...
-
Quality Assurance/Regulatory Affairs Associate
1 month ago
Markham, Ontario, Canada fluidigm Full timeJob Title: Quality Assurance/Regulatory Affairs AssociateJob Summary:We are seeking a highly motivated and detail-oriented Quality Assurance/Regulatory Affairs Associate to join our team. The successful candidate will be responsible for maintaining and ensuring that our quality system meets requirements for medical devices, and International Directives. This...
-
Regulatory Affairs Specialist
1 week ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs Intern RoleKenvue is currently recruiting for a Regulatory Affairs Intern to join our team.This position reports to the Associate Manager, Regulatory Affairs and is based at Markham, ON, Canada.The Regulatory Affairs Intern will be responsible for preparing submissions, responses to regulatory body queries, and filing annual renewal...
-
Regulatory Affairs Specialist
4 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will be responsible for preparing submissions, responding to regulatory body queries, and performing assessments to determine regulatory requirements for new projects.Key Responsibilities:Prepare...
-
Regulatory Affairs Specialist
4 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will be responsible for preparing submissions, responding to regulatory body queries, and performing assessments to determine regulatory requirements for new projects.Key Responsibilities:Prepare...
-
Regulatory Affairs Specialist
1 month ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will play a key role in supporting the development and implementation of regulatory strategies for our products.Key Responsibilities:Prepare and submit regulatory documents, including NHP PLAs, DIN...
-
Regulatory Affairs Specialist
2 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternThis role is part of the Regulatory Affairs team at Kenvue, a global leader in the development and manufacturing of consumer goods.The Regulatory Affairs Intern will be responsible for preparing submissions to regulatory bodies, responding to queries, and filing annual renewal packages.Key Responsibilities:Prepare submissions to...
-
Regulatory Affairs Specialist
1 month ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will be responsible for preparing submissions, responding to regulatory body queries, and performing assessments to determine regulatory requirements for new projects.Key Responsibilities:Prepare...
-
Regulatory Affairs Specialist
4 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will be responsible for preparing submissions, responding to regulatory body queries, and performing assessments to determine regulatory requirements for new projects.Key Responsibilities:Prepare...
-
Regulatory Affairs Specialist
4 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will be responsible for preparing submissions, responding to regulatory body queries, and performing assessments to determine regulatory requirements for new projects.Key Responsibilities:Prepare...
-
Regulatory Affairs Specialist
1 month ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternKenvue is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team. As a Regulatory Affairs Intern, you will be responsible for preparing submissions, responding to regulatory body queries, and performing assessments to determine regulatory requirements for new projects.Key Responsibilities:Prepare...
-
Regulatory Affairs Specialist
2 months ago
Markham, Ontario, Canada Kenvue Full timeJob SummaryWe are seeking a highly motivated and detail-oriented Regulatory Affairs Intern to join our team at Kenvue. As a Regulatory Affairs Intern, you will be responsible for supporting the preparation of regulatory submissions, responding to regulatory body queries, and maintaining various regulatory databases.Key ResponsibilitiesRegulatory Submissions:...
-
Regulatory Affairs Specialist
2 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternThis position reports to Associate Manager, Regulatory Affairs and is based at Kenvue.This position is a 12-month term.Key ResponsibilitiesPrepares submissions (e.g., NHP PLAs, DIN submissions, SNDSs, NCs, Level III notifications, Class II medical device applications/amendments, cosmetic notifications forms)Prepares responses to...
-
Regulatory Affairs Specialist
2 weeks ago
Markham, Ontario, Canada Kenvue Full timeRegulatory Affairs InternThis position reports to Associate Manager, Regulatory Affairs and is based at Markham, ON, Canada.This position is a 12-month term from 9/2024-9/2025.Key ResponsibilitiesPrepares submissions (e.g., NHP PLAs, DIN submissions, SNDSs, NCs, Level III notifications, Class II medical device applications/amendments, cosmetic notifications...
-
Quality Assurance Specialist
3 weeks ago
Markham, Ontario, Canada SGS Full timeJob DescriptionSGS is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring that our products and services meet the highest standards of quality and regulatory compliance.Key ResponsibilitiesReview and approve CCRs and manage SOP review and approval processResponsible...
-
Quality Assurance Specialist
3 weeks ago
Markham, Ontario, Canada SGS Full timeJob DescriptionSGS is seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring that our products and services meet the highest standards of quality and regulatory compliance.Key ResponsibilitiesReview and approve CCRs and manage SOP review and approval processResponsible...
-
Canada Senior Licensing Specialist
2 months ago
Markham, Ontario, Canada GE Vernova Full timeJob SummaryThe Canada Senior Licensing Specialist, Regulatory Affairs, will be responsible for various regulatory work scopes, including New Power Plant Licensing (NPPL), and will collaborate with GE-Hitachi Nuclear Energy Americas LLC (GEH) and Global Nuclear Fuels LLC (GNF) Engineering and R.Key ResponsibilitiesComplete regulatory work scopes, including...