Reckitt

1 month ago

Regulatory Operations Senior Associate

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 3 hours agoStatus: Live

Job Summary

Regulatory Operations Senior Associate within the Regulatory Affairs function to deliver and maintain regulatory dossiers for medical devices, coordinating cross-functional teams to ensure timely, compliant submissions and market registrations across multiple markets.

Location: Thailand

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

•Create, deliver and maintain medical device regulatory dossiers, ensuring alignment with regulatory strategy and timely market registrations across pipelines.
•Manage a complex regulatory landscape across markets by collaborating with regional/local teams and communicating requirements in clear business language to stakeholders.
•Deliver training and materials to prepare the business for current and future regulatory environments.
•Collaborate with RAS teams and cross-functional partners to develop and implement regulatory strategy and submissions, assessing global implications.
•Coordinate responses to regulatory authorities and lead projects across multiple markets to meet objectives and milestones.

Key Requirements

•Bachelor's degree or higher in a scientific field or equivalent experience.
•Strong knowledge of European Medical Device Regulation (MDR) or similar regulatory frameworks with a track record of successful projects.
•Experience delivering regulatory dossiers and registrations for medical devices across multiple markets.
•Ability to coordinate with cross-functional teams (Safety, Quality, Medical, Marketing, Supply, Packaging, R&D) to define submission requirements and timelines.
•Excellent communication skills with ability to translate regulatory information into stakeholder-friendly language and manage project timelines.

Experience:Medical devicesRegulatory affairs

Education:Bachelor's

Skills:CommunicationLeadershipCollaborationAttention to detailProject management

Company Brief

Reckitt

Global consumer goods company producing health, hygiene, and home products across well-known brands. Operates in multiple markets offering over-the-counter health, personal care, and household cleaning products to consumers worldwide.

Industry: FMCG

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Slough, United Kingdom

Founded: 1999

Website LinkedIn

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Reckitt

1 month ago

Regulatory Operations Senior Associate

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 3 hours agoStatus: Live

Job Summary

Location: Thailand

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

•Create, deliver and maintain medical device regulatory dossiers, ensuring alignment with regulatory strategy and timely market registrations across pipelines.
•Manage a complex regulatory landscape across markets by collaborating with regional/local teams and communicating requirements in clear business language to stakeholders.
•Deliver training and materials to prepare the business for current and future regulatory environments.
•Collaborate with RAS teams and cross-functional partners to develop and implement regulatory strategy and submissions, assessing global implications.
•Coordinate responses to regulatory authorities and lead projects across multiple markets to meet objectives and milestones.

Key Requirements

•Bachelor's degree or higher in a scientific field or equivalent experience.
•Strong knowledge of European Medical Device Regulation (MDR) or similar regulatory frameworks with a track record of successful projects.
•Experience delivering regulatory dossiers and registrations for medical devices across multiple markets.
•Ability to coordinate with cross-functional teams (Safety, Quality, Medical, Marketing, Supply, Packaging, R&D) to define submission requirements and timelines.
•Excellent communication skills with ability to translate regulatory information into stakeholder-friendly language and manage project timelines.

Experience:Medical devicesRegulatory affairs

Education:Bachelor's

Skills:CommunicationLeadershipCollaborationAttention to detailProject management

Company Brief

Reckitt

Industry: FMCG

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Slough, United Kingdom

Founded: 1999

Website LinkedIn