At HARTMANN, we’re all in to *help*, *care*, *protect* and *grow*. We
support healthcare professionals, that they can focus on what really
matters: to positively impact people´s life. We realize solutions that
make a difference. And with your commitment you can grow on your job every
day. At HARTMANN we believe in the difference you can make.

Join our team as

*Manager Regulatory Affairs Operations (w/m/d)*

DEU-Heidenheim

Join HARTMANN and become part of a global team that’s shaping the future
of healthcare. As a *Manager **Regulatory Affairs Operations (f/m/d)* we
offer you a varied and challenging position in an international environment
in the *Division Risk Prevention*. Here you can develop your skills and
play an active role in ensuring product quality and regulatory product
conformity. If you are also enthusiastic about our meaningful product
portfolio, we should get to know each other.

-Responsibilities: -

· In this cross-functional and global role, you will collaborate with
teams including R&D, Quality Assurance, Manufacturing, and Marketing to
ensure the implementation of products on time according to regulatory
requirements
· You will assume portfolio responsibility for the products under your
care
· Ensure compliance throughout the product lifecycle
· Global monitoring and improvement of regulatory product documentation
and conformity assessments
· You will be responsible for driving the optimization of the IT
infrastructure related to regulatory documentation management
· Provide strategic and technical consulting on regulatory issues
· Evaluation of product-related regulatory requirements with focus on risk
management, labeling and post-market surveillance
· Support complaint management

-*Qualification:*-

· University degree in science or technical sciences or an equivalent
qualification
· Professional experience in the medical device environment or another
regulatory field of work
· Proven experience with MDR and ISO 13485
· Knowledge and/or experience in the areas of medical devices, technical
documentation and regulatory product documentation, conformity assessment
and post-market surveillance
· Familiarity with FDA regulations and guidelines is desirable
· A strong interest in and knowledge of electronic regulatory document
control and management systems and associated processes
· Open and competent attitude when working with internal partners
· Strong communication skills with an open and professional attitude when
collaborating with both internal and external partners
· IT affinity and proficiency with the MS Office package
· Fluent written and spoken German and English

-*Benefits*-

· Flexible working conditions, such as flexible working hours and mobile
working
· International Mobile Working
· Attractive ways of combining work and family life, e.g. childcare
subsidy
· 30 days paid leave per year, plus special leave for exceptional life
events as well as vacation pay and special annual payment according to
collective agreement
· Company pension plan with attractive employer contribution incl.
matching model for deferred compensation
· Plenty of parking spaces, canteen with café bar and ongoing offers in
the employee shop
· Access to over 6000 fitness and yoga studios, swimming pools as well as
Crossfit and bouldering halls (EGYM Wellpass)
· Various health and fitness offers, e.g. skin cancer screenings, online
courses for mental health, massage offers, yoga during lunch break etc.
· Job Bike Leasing
· Attractive discounts on e.g. travel, fashion and technology via our
corporate benefits platform