Ir à oferta completa

INTERNSHIP: REGULATORY AFFAIRS & COMPLIANCE INTERN

Lisboa - Lisboa

Descrição da oferta de emprego

Descripción del puesto.
Job Title Internship.
Regulatory Affairs & Compliance Intern Job Description Location.
Lisbon Working time.
39 hours/week Start date.
as soon as possible Type.
1-year, remunerated internship Your role.
* Maintaining Expertise.
Continuously enhance personal competencies, scientific knowledge, and technical skills in specific sections of the technical documentation of Medical Devices to ensure domain expertise within the RAC team.
Technical Documentation Assessment.
Evaluate technical documentations for a broad range of medical devices covering product development, launch, and maintenance.
Provide critical feedback to Philips manufacturers and follow up with them to ensure that the devices are designed to be state-of-the-art, safe, effective, and meet all required legislations, standards, and guidance document throughout product life-cycle.
Product Registration.
When required, registration of products at jurisdictional databases.
* Detail elements of the team and stakeholders for this role.
You are part of the Regulatory Affairs and Compliance Team, Philips Medical Systems Nederland B.
.
Best, The Netherlands.
You work under the direction of the Head of Regulatory Affairs & Compliance Team.
While you will work remotely, you will be located in the region of Lisbon and be affiliated to the Philips office in Lisbon (Portugal).
Here you will work with other team members from the Regulatory Affairs and Compliance Team.
* This internship is a stepping stone for those interested in a career in the medical device industry, offering valuable experience and potential career development opportunities.
It offers the following opportunities.
Industry Insights.
Gain insights and knowledge into the Research & Development, testing, risk management, manufacture, clinical and post market safety and performance assurance, and Regulatory Affairs of a wide range of Medical Devices of low, moderate, and high risk.
Cross-functional Interaction.
This internship provides a unique opportunity to interact with different cross-functional teams within various Philips manufacturing units, offering a comprehensive understanding of the Medical Device industry.
Leadership Development.
The internship cultivates systems thinking; skills in application of relevant regulations and standards; a focus on patient safety and quality; develop effective communication skills; and confidence in project ownership and management.
Career Development.
Open up career development possibilities within Philips or elsewhere in the Regulatory Affairs / Clinical Affairs / Quality Assurance/ Usability/ Biocompatibility/ Research & Development Medical Devices software and hardware.
You're the right fit if.
1.
Education.
A research-minded Post Graduate having completed a Master of Science degree from a Technical University.
Students of Biomedical Engineering, any scientific discipline, or Engineering degree are of special interest.
2.
Skills.
An analytical thinker who is keen to learn and grow.
A perseverant and proactive team player who can work both independently and within a team.
Proficiency in Portuguese and English is a must.
Skills in French is an advantage.
3.
Experience.
Previous internship in regulatory affairs or clinical affairs in medical devices, pharmaceuticals, cosmetics, or other fields would be an advantage.
4.
Passion.
Above all, a strong motivation to bring safe and effective medical devices to patients and a passion for healthcare.
About Philips We are a health technology company.
We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve.
Do the work of your life to help the lives of others.
* Learn more about our business.
* Discover our rich and exciting history.
* Learn more about our purpose.
If you're interested in this role and have many, but not all, of the experiences needed, we encourage you to apply.
You may still be the right candidate for this or other opportunities at Philips.
Learn more about our commitment to diversity and inclusion here.
#LI-EU
Ir à oferta completa

Detalhes da oferta

Empresa
  • Indeterminado
Localidade
Endereço
  • Indeterminado - Indeterminado
Data de publicação
  • 10/04/2024
Data de expiração
  • 09/07/2024
Junior Development Engineer–Instrumentation-IEFP Internship
biosurfit

Write technical documentation such as test reports and test procedures; basic electronics and instrumentation tasks; close collaboration with spinit® cartridge development team; compliance with regulatory requirements for r&d; projects; when required, assistance with existing projects......

Internship Sales & Administration Support English/ french
Eurofirms

Our commitment and involvement, together with constant technological innovation, has allowed us to position ourselves as one of the leading national human resources companies for an important company in the automobile sector, located in the area of maia, we are hiring an internship sales and administration......

Certified Accountant - Blue&Green
Blue&Green

Reporting to the accounting responsible, will have the following responsibilities : manage month, quarter and year end activities, controls and report;regular posting of business transactions, ensuring their accuracy and compliance with accounting rules and internal procedures;assist in the preparation......

Patch Management Analyst
Newin

· participate in routine audits to record patch levels and create reports to meet compliance... responsibilities strategy & planning · develop patch maintenance schedules to meet client requirements to maintain compliance for software updates and contracts... · complete emergency (zero day) patch deployments......

Estágio profissional iefp: consultor de esg
Sustentare

Principais funções: - apoio na execução de análises de empresas, identificando o seu nível de compliance com uma base de critérios esg; - estruturar processos de recolha de informação esg; - realizar análises de dados corporativos, e calcular indicadores esg; - redigir textos relacionados com as diversas......

Video content analyst (m,f) german or dutch
Personalbüro u. herrmann

Start: asap duties and responsibilities: review user reports regarding website content daily content compliance monitoring and corrective measures application make well-balanced decisions and help resolve inquiries to defined policies and procedures propose solutions to improve the support of user community......

German or Dutch Video Content Analyst
SpotOn Connections

Day-to-day responsibilities: review user reports regarding website content analyze and identify content that is not in compliance with requirements and flag for action in a timely manner make well-balanced decisions and help resolve inquiries to defined policies and procedures use market specific knowledge......

DUTCH VIDEO CONTENT ANALYST
SpotOn Connections

Day-to-day responsibilities:review user reports regarding website contentanalyze and identify content that is not in compliance with requirements and flag for action in a timely mannermake well-balanced decisions and help resolve inquiries to defined policies and proceduresuse market specific knowledge......

German Video Content Analyst
SpotOn Connections

Day-to-day responsibilities:review user reports regarding website contentanalyze and identify content that is not in compliance with requirements and flag for action in a timely mannermake well-balanced decisions and help resolve inquiries to defined policies and proceduresuse market specific knowledge......

German speaking Customer and Sales Support Officer
SpotOn Connections

Systems; adhere to all company policies and procedures, corporate security policies, regulatory guidelines, industry service standards and codes of conduct; keeping records as required; issuing of new cards and renewal processes... assistance with gathering of data/information for the company (via......