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Regulatory Affairs and QMS Lead (Freelance)

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Germany

Offer summary

Qualifications:

University degree in biomedical science or related field, 7+ years experience in MDD/MDR and FDA submissions, Knowledge of EU medical device regulations and Quality Management Systems.

Key responsabilities:

Develop regulatory strategy for compliance with laws and regulations
Optimize QMS focusing on processes like change control, risk management
Lead global regulatory approval processes and develop responses for inquiries
Ensure compliance with applicable regulatory requirements and handle incident reporting
Promote awareness of regulatory requirements throughout the organization

apoQlar

51 - 200 Employees

See more apoQlar offers

Job description

Make a positive impact in the global healthcare community with cutting-edge medical mixed reality technology. 

About Us

apoQlar is the developer of a medical mixed reality platform that is revolutionizing how medicine is practiced, experienced, learned, and shared. Our flagship product, VSI HoloMedicine®, is a medically certified software platform that leverages the Microsoft HoloLens hardware to transform medical images, clinical workflows, and medical education into an interactive 3D mixed reality environment.

With offices in Miami, Poznan, Singapore and our headquarters in Hamburg we are dedicated to revolutionizing the healthcare industry by leveraging cutting-edge technology and innovative solutions.

We are currently looking for an enthusiastic and motivated individual to join our team in Hamburg (onsite/hybrid) to expand our Regulatory & Quality Management team on freelance basis. You will take a leading role within the Regulatory & Quality Management team and work closely with C-Level as well as our engineering teams to ensure our mixed reality platform is in compliance with regulatory and statutory requirements.

Responsibilities Include

Develop and lead the regulatory strategy to ensure compliance with applicable laws, regulations and ensure a fast and efficient certification of new product developments.
Maintain and optimize the current QMS and RA framework, focusing on specific processes such as change control, design controls, verification and validation, and risk management.
Lead the regulatory approval processes globally.
Lead the development of regulatory responses for questions from notified bodies, global regulators and regulatory representatives upon review of submissions in relation to the technical dossier.
Implement regulatory requirements in accordance with EU MDR 2017/745.
Lead risk management activities and work closely with the risk management team through the life cycle of medical device software.
Participate in and support external/internal audits and responses to audit findings as appropriate.
Ensure compliance with the current regulatory procedures and update the procedures when new regulatory requirements are determined.
Monitor the new/revised applicable regulatory requirements, standards, guidance, and common specifications.
Handle serious incident and adverse event reporting.
Ensure that the communication with Notified Bodies and Regulatory Authorities is effective and that all the required information is provided.
Ensure that marketing communication is according to regulatory requirements.
Ensure that regulatory and statutory requirements are fully met across the whole organization.
Ensure the promotion of awareness of applicable regulatory requirements throughout the organization.
Act as appointed Person Responsible for Regulatory Compliance (PRRC).

Qualifications

University degree in biomedical science, engineering, pharmacy, or any other applied natural sciences.
7+ years of professional experience including MDD/MDR and FDA submissions.
Proficient practical FDA 510K application knowledge and a proven track record of associated products.
Proficient knowledge of EU medical device regulations and Quality Management Systems for medical devices.
Knowledge of MDSAP, ISO 13485, IEC 62304 and ISO 14971.
Experience in communication with authorities and notified bodies.
In-depth knowledge of Software Lifecycle Processes, including expertise in implementing the requirements of the IEC 62304 standard and AAMI TIR45 guidance (agile).
Extensive experience in Software as a Medical Device (SaMD), covering design controls, risk management, verification and validation, SOUP (Software of Unknown Provenance), and Software Configuration Management (SCM).
Demonstrated ability to maintain and streamline QMS for seamless use across the organization, ensuring a sustainable and compliant system.
Experience in communication with healthcare professionals.
Strong analytical skills to evaluate product compliance and interpret regulatory guidelines.
Ability to collaborate effectively with internal specialists and other external consultants (if required), ensuring alignment and cooperation.
Experience in external and internal Audits.
Fluency in English is a requirement, German is a huge plus.

Why Us?

Chance to work with new and exciting technologies.
Opportunity to positively impact the lives of patients, students, and surgeons around the world.
Chance to not just shape but also create an entirely new market in healthcare using medical mixed reality.
Work alongside a multicultural and international team – over 10 countries represented in our office.
A flat hierarchy with direct access to the founding team and C-Level.
High degree of ownership with the opportunity to drive projects forward on your own or with a team.
Competitive compensation structure and ability to grow quickly within an advancing team.

Are you interested in helping us shape an entirely new market in healthcare and advancing next generation medical technology? Then we look forward to hearing from you!