Student Assistant in QA/RA

Are you a motivated student looking for a student job while studying? Do you want to gain valuable experience within quality, regulatory and clinical for medical devices?

As our new Student Assistant, you will support the departments for Quality Assurance, Regulatory Affairs, Clinical Development and Clinical Operations in day-to-day business processes and tasks. You will gain hands-on experience in a dynamic work environment working with very experienced teams with diverse backgrounds.

Your main tasks will include:

• Monitoring of changes to regulatory standards and assist with performing analysis of the change
• Performing ad-hoc task related to optimization of our document handling system
• Keeping our reference manager system up to date
• Assistance to various clinical studies including preparation on study binders, ordering and packaging of products for clinical investigations, monitoring of databases, keeping track of devices in the study
• Performing administrative ad-hoc tasks.

We expect that you will work between 8-16 hours per week from our office in Allerød. We provide flexibility to meet your educational responsibility as we recognize the value of your study.

Qualifications:

We are looking for a student with a passion for medical devices and an interest in working with regulatory compliance. You are studying for a bachelor’s or master’s degree in a field of natural science such as biomedical, engineering, or similar.

On a personal level, you are thorough and systematic, and you thrive with driving tasks independently to the finish line. You are an advanced user in the MS Office package and willing to learn to work in new IT systems.

Given the international environment of UNEEG medical, English is our corporate language. You will use English in your daily work, which requires that you speak and write English at a high level.

About the department:

You will be part of the Quality Assurance & Regulatory Affairs (QA/RA) department, which has the overall responsibility for ensuring regulatory and quality compliance, contributing to the production of high-quality products and their regulatory approval. We are involved from the beginning of device design and remain involved throughout the device life cycle.

By becoming our new Student Assistant, you will get great opportunities to work with a wide array of tasks, and you will get experience within the different department areas. You will be surrounded by individuals from diverse backgrounds, further enriching your professional growth.

Contact:

For more details about the job, please contact Senior Director QA/RA, Camilla Wismar, at +45 40184937.

Application:

Deadline: 28 April 2024.

Kindly note that applications will be reviewed continuously, and interviews conducted on a rolling basis.

Please include a written application together with your CV. We accept applications in both Danish and English language.

About UNEEG medical A/S:

UNEEG medical A/S is an entrepreneurial and ambitious company specializing in providing the epilepsy community with more accurate knowledge of seizures to support improvement in epilepsy care, ultimately aiming at improving patients’ quality of life. Our unique subcutaneous EEG solution for remote monitoring of brain activity was CE marked in 2019 and our continued international growth and technology roadmap ambitions will require several new functions and competencies in the years to come.

UNEEG medical A/S was founded in 2005 and is today owned by the families behind the large hearing aid company Widex/WS Audiology. We currently employ approximately 120 people in Europe – the majority of these are situated in our headquarters in Allerød, Denmark. Our employees represent various cultures, backgrounds, skills, and years of experience.

Are you a motivated student looking for a student job while studying? Do you want to gain valuable experience within quality, regulatory and clinical for medical devices?

Are you a motivated student looking for a student job while studying? Do you want to gain valuable experience within quality, regulatory and clinical for medical devices?
As our new Student Assistant, you will support the departments for Quality Assurance, Regulatory Affairs, Clinical Development and Clinical Operations in day-to-day business processes and tasks. You will gain hands-on experience in a dynamic work environment working with very experienced teams with diverse backgrounds.
Your main tasks will include:

Monitoring of changes to regulatory standards and assist with performing analysis of the change

Performing ad-hoc task related to optimization of our document handling system

Keeping our reference manager system up to date

Assistance to various clinical studies including preparation on study binders, ordering and packaging of products for clinical investigations, monitoring of databases, keeping track of devices in the study

Performing administrative ad-hoc tasks.

Monitoring of changes to regulatory standards and assist with performing analysis of the change
Performing ad-hoc task related to optimization of our document handling system
Keeping our reference manager system up to date
Assistance to various clinical studies including preparation on study binders, ordering and packaging of products for clinical investigations, monitoring of databases, keeping track of devices in the study
Performing administrative ad-hoc tasks.
We expect that you will work between 8-16 hours per week from our office in Allerød. We provide flexibility to meet your educational responsibility as we recognize the value of your study.
Qualifications:
Qualifications:
Qualifications:
We are looking for a student with a passion for medical devices and an interest in working with regulatory compliance. You are studying for a bachelor’s or master’s degree in a field of natural science such as biomedical, engineering, or similar.
On a personal level, you are thorough and systematic, and you thrive with driving tasks independently to the finish line. You are an advanced user in the MS Office package and willing to learn to work in new IT systems.
Given the international environment of UNEEG medical, English is our corporate language. You will use English in your daily work, which requires that you speak and write English at a high level.
About the department:
About the department:
About the department:
You will be part of the Quality Assurance & Regulatory Affairs (QA/RA) department, which has the overall responsibility for ensuring regulatory and quality compliance, contributing to the production of high-quality products and their regulatory approval. We are involved from the beginning of device design and remain involved throughout the device life cycle.
By becoming our new Student Assistant, you will get great opportunities to work with a wide array of tasks, and you will get experience within the different department areas. You will be surrounded by individuals from diverse backgrounds, further enriching your professional growth.
Contact:
Contact:
Contact:
For more details about the job, please contact Senior Director QA/RA, Camilla Wismar, at +45 40184937.
Application:
Application:
Application:
Deadline: 28 April 2024.
Kindly note that applications will be reviewed continuously, and interviews conducted on a rolling basis.
Please include a written application together with your CV. We accept applications in both Danish and English language.

About UNEEG medical A/S:
About UNEEG medical A/S:
About UNEEG medical A/S:
About UNEEG medical A/S:
UNEEG medical A/S is an entrepreneurial and ambitious company specializing in providing the epilepsy community with more accurate knowledge of seizures to support improvement in epilepsy care, ultimately aiming at improving patients’ quality of life. Our unique subcutaneous EEG solution for remote monitoring of brain activity was CE marked in 2019 and our continued international growth and technology roadmap ambitions will require several new functions and competencies in the years to come.
UNEEG medical A/S is an entrepreneurial and ambitious company specializing in providing the epilepsy community with more accurate knowledge of seizures to support improvement in epilepsy care, ultimately aiming at improving patients’ quality of life. Our unique subcutaneous EEG solution for remote monitoring of brain activity was CE marked in 2019 and our continued international growth and technology roadmap ambitions will require several new functions and competencies in the years to come.
UNEEG medical A/S was founded in 2005 and is today owned by the families behind the large hearing aid company Widex/WS Audiology. We currently employ approximately 120 people in Europe – the majority of these are situated in our headquarters in Allerød, Denmark. Our employees represent various cultures, backgrounds, skills, and years of experience.
UNEEG medical A/S was founded in 2005 and is today owned by the families behind the large hearing aid company Widex/WS Audiology. We currently employ approximately 120 people in Europe – the majority of these are situated in our headquarters in Allerød, Denmark. Our employees represent various cultures, backgrounds, skills, and years of experience.