Reckitt

1 month ago

Regulatory Operations Associate

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 2 hours agoStatus: Live

Job Summary

Regulatory Operations Associate supports the compilation, preparation, review and submission of regulatory documents for medical device dossiers, collaborating with global Regulatory Affairs, RAS Strategy and cross-functional teams to launch new innovations, maintain licenses, and ensure compliance across product life cycles in Reckitt’s global footprint.

Location: Thailand

Workplace: Onsite

Employment Type: Full time

Job Function: Quality & Regulatory (Non-Software)

Key Responsibilities

•Create, deliver and maintain medical device regulatory dossiers in line with the agreed regulatory strategy to achieve in-market registrations/launches and ensure pipeline compliance.
•Work in partnership across RAS teams to develop, communicate, and implement the regulatory strategy in collaboration with cross-functional project team; prepare and support submission of registration dossiers with global implications.
•Support and deliver training to business partners on regulatory environment and implications.
•Collaborate with other X-functional technical functions (Safety, Quality, Medical, Marketing, Supply, Packaging and R&D) and local teams to define submission requirements in an efficient and timely manner.
•Coordinate responses to questions from regulatory authorities and lead cross-market projects to meet objectives and milestones.

Pay and Benefits

Perks:Life Insurance

Key Requirements

•Prior experience in Medical Device Regulation or a similar regulatory area.
•Knowledge of global product development and maintenance for Reckitt products, including current and emerging rules, regulations and guidelines impacting medical device dossiers/regulatory file generation.
•Degree level education in a scientific field or equivalent experience.
•Ability to develop peer-to-peer partnerships across RAS and all cross-functional teams.
•Ability to deliver regulatory dossiers and manuscripts in line with regulatory strategy and timelines.

Experience:Medical devicesRegulatory affairs

Education:Associate's

Skills:Attention to detailCross-functional collaborationRegulatory strategyCommunicationProject management

Languages:English

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 Associate

✓ Verified Job

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

Source: Company careers pageValidated by: Fursa AI

Last checked: 2 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 in line with the agreed regulatory strategy to achieve in-market registrations/launches and ensure pipeline compliance.
•Work in partnership across RAS teams to develop, communicate, and implement the regulatory strategy in collaboration with cross-functional project team; prepare and support submission of registration dossiers with global implications.
•Support and deliver training to business partners on regulatory environment and implications.
•Collaborate with other X-functional technical functions (Safety, Quality, Medical, Marketing, Supply, Packaging and R&D) and local teams to define submission requirements in an efficient and timely manner.
•Coordinate responses to questions from regulatory authorities and lead cross-market projects to meet objectives and milestones.

Pay and Benefits

Perks:Life Insurance

Key Requirements

•Prior experience in Medical Device Regulation or a similar regulatory area.
•Knowledge of global product development and maintenance for Reckitt products, including current and emerging rules, regulations and guidelines impacting medical device dossiers/regulatory file generation.
•Degree level education in a scientific field or equivalent experience.
•Ability to develop peer-to-peer partnerships across RAS and all cross-functional teams.
•Ability to deliver regulatory dossiers and manuscripts in line with regulatory strategy and timelines.

Experience:Medical devicesRegulatory affairs

Education:Associate's

Skills:Attention to detailCross-functional collaborationRegulatory strategyCommunicationProject management

Languages:English

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