Senior Regulatory Affairs Specialist

Collabera
Saint Paul, MN, US
Full-time

Job Description

Job Description

Perform assigned regulatory activities including submissions / responses to country authorities.

Daily Responsibilities - Job Description suppliers should use :

  • Plan and prepare documents for EU MDR Technical File original submissions or responses to Notified Body for existing Technical Files under review.
  • Assist in strategy implementation and operations for regulatory affairs activities, including development of EU MDR Technical File submissions and responses to Notified Bodies.
  • Assist in maintaining Regulatory records and files.
  • Review product changes as assigned and assess required EU MDR submissions / notifications.

Educational Requirements :

  • BA Degree required, preferably in a science, engineering or technology discipline.
  • Work Experience Requirements : 3-5 years experiences in Medical Device Regulatory Affairs Top

Skills :

  • Strong oral communication and interpersonal skills
  • Proficient in technical writing
  • Excellent organizational ability, capability to manage multiple, dynamic projects simultaneously.
  • MS Office Suite including an Intermediate level with Excel using Pivot Tables, Creating Trackers in Excel and monitoring these / Conditional Formatting.

Company Description

Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data / AI.

With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.

Company Description

Collabera is a Global Digital Solutions Company providing Software Engineering Solutions for the world's most tech-forward organizations in the areas of Engineering, Cloud and Data / AI.

With its roots serving the engineering needs of the world's most recognized businesses in Technology, Financial Services, Telecom and Healthcare, Collabera today operates across 60 locations in 11 countries, serves 30% of the Fortune 500, and has exceeded the industry growth rate by 3-4x for several years.

30+ days ago
Related jobs
Promoted
Ameriprise Financial, Inc
Minneapolis, Minnesota

The Senior Regulatory Reporting Specialist role will be part of the Business Controls team within the Trading department. The Specialist will perform complex trade reporting in accordance with requirements for all security types, with a focus on fixed income, along with interpreting regulatory trade...

Promoted
Boston Scientific Gruppe
Saint Paul, Minnesota

Actively participate in various Quality System Community of Practice teams representing Regulatory Affairs interests, assessing impact, and bringing awareness to Regulatory Teams. The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory prod...

Abbott
Saint Paul, Minnesota

Senior Regulatory Affairs Specialist. Master’s Degree in Regulatory Affairs preferred and may be used in lieu of direct regulatory experience. Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes. Understand, investigate and evaluate regulatory ...

OSH-Clin-Clinical Research Medical Science & Regulatory Affairs (CMRA)
Mounds View, Minnesota
Remote

The Senior Medical Safety Specialist works with minimal supervision on a range of medical safety activities of varying complexity in collaboration with Medical Safety team members and other functions, including Regulatory, Quality/Post-Market vigilance, Risk Management, Complaint Handling, Product D...

Bio-Techne
Minneapolis, Minnesota

The Advanced Regulatory Affairs Specialist provides independent support to senior regulatory staff to submit regulatory filings. This position will demonstrate advanced knowledge of regulatory changes and assist with communication to customers and regulatory authorities. Assist with regulatory respo...

Volt
New Hope, Minnesota

Regulatory Affairs Specialist II at Plymouth, MN. As a Regulatory Affairs Specialist II, you will:. Support daily Regulatory Affairs function eg; compliance to 21 CFR 820,807,803 ISO 13485 requirements, Company policies, operating procedures, processes, promotional task assignments into windchill an...

Volt
New Hope, Minnesota

Regulatory Affairs Specialist II at Plymouth, MN. As a Regulatory Affairs Specialist II, you will:. Support daily Regulatory Affairs function eg; compliance to 21 CFR 820,807,803 ISO 13485 requirements, Company policies, operating procedures, processes, promotional task assignments into windchill an...

Volt
New Hope, Minnesota

Regulatory Affairs Specialist II at Plymouth, MN. As a Regulatory Affairs Specialist II, you will:. Support daily Regulatory Affairs function eg; compliance to 21 CFR 820,807,803 ISO 13485 requirements, Company policies, operating procedures, processes, promotional task assignments into windchill an...

ERM
Minneapolis, Minnesota

For the Managing Consultant, Environmental Regulatory Specialist (Senior Level) position, we anticipate the annual base pay of $76,000 – $94,860 (USD). Environmental Regulatory Specialist. Federal Energy Regulatory Commission (FERC). Research, analyze and compile data for permit applications and rep...

Medtronic
Mounds View, Minnesota

Medtronic Structural Heart is seeking an experienced and highly motivated Senior Manager of Regulatory Affairs to play a crucial role in the development and execution of global regulatory strategies for innovative transcatheter valve technologies. Senior Manager, Regulatory Affairs - Structural Hear...