Regulatory Affairs Specialist - Aachen, Deutschland - Abiomed

Abiomed

Geprüftes Unternehmen

Aachen, Deutschland

vor 1 Woche

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Abiomed, an innovative medical device company, is focused on recovering hearts and saving lives.

We have a single guiding mission:
"Patients First." With corporate headquarters in Danvers, Massachusetts, offices in Aachen & Berlin, Germany and Tokyo, Japan, Abiomed's 1,700 employees form one of the fastest growing medical technology companies in the world. Abiomed attracts and retains exceptional talent with our collaborative culture, passion for our work, and a strong commitment to employee professional development.

Principal Duties and Responsibilities:

The Regulatory Affairs Specialist will be responsible for submissions in Europe and the Middle East, potentially including emerging markets in Eastern and South-East Europe and Africa, as needed as well as project team participation.

The Regulatory Affairs Specialist will also act as a key liaison with the regulatory agencies as needed.

Be passionate about regulatory affairs in support of the production of stateoftheart medical devices
Be energized by working for a worldclass manufacturer and collaborating on crossfunctional teams
Recognize the importance of building and maintaining strong interpersonal relationships
Understand the impact of global registrations and product commercialization
Develop and execute submissions for new products

Key Responsibilities:

Execute regulatory planning and ensure alignment with business and functional goals and priorities
Support development and implementation of regulatory strategies throughout the product lifecycle that are consistent with business unit goals and objectives
Actively participate on project teams as assigned
Conduct presentations and negotiations to agency reviewers as needed
Review and interpret regulatory rules as they relate to company products and procedures, testing or records keeping and ensure that they are communicated through company policies and procedures
Review and approve changes to manufacturing processes and products to ensure compliance with RA guidelines of assigned jurisdictions
Provide input to the product development and engineering teams to ensure that RA requirements are fully understood and mitigated as part of the product development and the engineering change process
Communicate regulatory project status to internal stakeholders
Follow changes of the regulatory landscape, identify impact to the company and develop solutions to maintain regulatory compliance

Qualifications:

Degree in engineering or science required, advanced degree preferred
At least 2 years of regulatory affairs experience with a cardiovascular device company preferred
Experience in submissions following the European Medical Device Directive 93/42/EEC or Active Implantable Medical Device Directive 90/385/EEC
First experience with transfer to the EU Medical Device Regulation 2017/74
Experience in regulatory submission preparation
Project Management experience preferred
Ability to communicate ideas and information clearly, effectively and frequently (oral and written)
Ability to exercise independent judgment in methods, techniques and evaluation criteria for obtaining results
Must be proficient in Microsoft Office Suite
Fluent in English and German

We offer:

Pleasant, open corporate culture with a strong mission: "Recovering Hearts, Saving Lives"
Comprehensive induction program with structured onboarding plan throughout the orientation phase
Company pension allowance of up to 1,500 euros per year and capitalforming benefits
Abiomed shares at a preferential price
Benefit packages for occupational disability insurance and company group accident insurance
Full cost coverage for a job ticket in the Aachen or Berlin area
Various health programs and a leasing option for a job bike

ABIOMED is an Equal Employment Opportunity employer.

We are committed to the policy of providing equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, disability or national origin.