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Junior Regulatory Affairs Specialist
Bayer —Carnaxide
Post-approval activities and regulatory submissions for medicines, medical devices, food supplements and cosmetics. Support with advertising materials revision.
Regulatory Affairs Specialist – Medical Devices (SaMD)
UpHill —1990 Lisboa
Build, maintain and scale our regulatory and quality framework. EU MDR (Medical Device Regulation). FDA (Food and Drug Administration, US) requirements for SaMD…

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Junior Regulatory Affairs Specialist

Bayer -
Carnaxide

Candidate-se agora

Detalhes da oferta

Descrição completa da oferta

Junior Regulatory Affairs Specialist

Main Purpose:

To undertake regulatory tasks to support the Consumer Health Regulatory Team in Iberia (Spain & Portugal) including but not limited to:

1. Post-approval activities and regulatory submissions for medicines, medical devices, food supplements and cosmetics

2. Overall management and technical support of Regulatory databases.

3. Supporting role in the financial tracking and recording within respective systems/documents

4. Responsibility in preparation and implementation of artworks with regards to management of internal systems

5. Management of translations of text and artwork as appropriate

6. Support with advertising materials revision

Main Working Relationships:

Iberia/EUN/Global Regulatory Teams

Iberia Business e.g. Medical Information, Procurement, IT, legal, sales, marketing, trade marketing, quality, supply...

External Health authorities and other competent authorities

Industry associations

Key Tasks/Responsibilities

1. Management of submissions to the authority, including variations, renewals, notifications and other regulatory submissions as required for a portfolio that includes Medicines, Medical Devices, Food Supplements and Cosmetics.

2. Management of all Regulatory trackers/databases

3. Management of artwork generation & implementation in respective internal systems.

4. Notifying authority of end of commercialisations

5. To undertake special projects (e.g. regulatory intelligence, competitor information, tracking new legislation, submission support) and support regulatory team as needed for internal and external meetings.

6. Proofing of regulatory documents as required, including management of any translations.

7. Supporting the monitoring of Iberia RA budget including raising requisitions and processing invoices/payments of fees when required

8. Ensure compliance with EU regulatory requirements, codes of practice, global SOPs and internal guidelines.

9. Filing and archiving of authority correspondence (e.g., authority confirmation emails, approval letters, RFI responses) in appropriate product variation folders and databases.

10. Supporting post-approval actions both internal (e.g., artwork updates, SmPC/PIL updates, HA/local medicines database updates, compliance checks on artwork)

11. Support with the revision of advertising materials and obtain external validations, if applicable.

Skills & qualifications:

Education: Science degree (Pharmaceutical sciences preferred)

Excellent knowledge of IT in order to work with databases and to prepare high quality documents

Ability to work in a team

Ability to organise and plan effectively with good communication skills

Commercial awareness and good information management skills

Customer focus and proactivity

Good commercial awareness

Ability to organize and plan effectively

Fluent in Portuguese and English. Working knowledge of Spanish is desired but not mandatory

Application Period:

31/07/2026 - 14/08/2026

Reference Code:

872591

Division:

Consumer Health

Location:

Portugal : Estremadura : Carnaxide

Functional Area:

Regulatory Affairs

Position Grade:

Employment Type:

Regular

Work Time:

Regular

Contact Us

Address

Telephone

E-Mail

Rua Quinta do Pinheiro, 5

[email protected]

Candidate-se agora

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regulatory affairs specialist vagas para: porto salvo

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