Regulatory Affairs Manager page is loaded
Regulatory Affairs Manager
Apply locations Reading time type Full time posted on Posted Yesterday time left to apply End Date: March 1, 2025 (29 days left to apply) job requisition id R2775678 Regulatory Affairs Lead UK
at
Sanofi
(specifically for their
Opella
business unit). This role involves overseeing the regulatory affairs for the Consumer Healthcare (CHC) portfolio, focusing on OTC products, vitamins, and supplements in the UK. The responsibilities include: Key Responsibilities:
Portfolio Management: Preparing and managing marketing authorization applications. Ensuring product labels, leaflets, and summaries are compliant with regulations. Overseeing product packaging to meet regulations. Reviewing promotional materials for compliance. Managing OTC switches and local regulatory strategies. Regulatory Compliance: Keeping product packaging and information up to date in line with current licenses. Implementing mandatory SOPs and ensuring regulatory compliance across the organization. Regulatory Environment Influence: Tracking and responding to emerging regulatory changes. Participating in local trade associations and influencing the regulatory landscape. Building relationships with health authorities to support the company's strategy. Innovation and Risk Management: Contributing to innovation programs and identifying regulatory risks. Overseeing the approval of risk management plans and related materials. About You:
A
university scientific degree
is required. Knowledge of
UK and international regulatory affairs
and
CHC regulations . Experience with regulatory aspects of medicines, food supplements, and medical devices. Strong
matrix team
working skills and ability to drive regulatory excellence. Additional language skills would be a plus. Company Culture and Benefits:
Sanofi highlights its commitment to progress, diversity, and inclusion, offering equal opportunities for all candidates. The role is based in
Reading
and offers a
hybrid work arrangement . This position plays a key role in ensuring Sanofi's products comply with regulations while influencing and shaping the regulatory landscape in the UK.
#J-18808-Ljbffr
Apply locations Reading time type Full time posted on Posted Yesterday time left to apply End Date: March 1, 2025 (29 days left to apply) job requisition id R2775678 Regulatory Affairs Lead UK
at
Sanofi
(specifically for their
Opella
business unit). This role involves overseeing the regulatory affairs for the Consumer Healthcare (CHC) portfolio, focusing on OTC products, vitamins, and supplements in the UK. The responsibilities include: Key Responsibilities:
Portfolio Management: Preparing and managing marketing authorization applications. Ensuring product labels, leaflets, and summaries are compliant with regulations. Overseeing product packaging to meet regulations. Reviewing promotional materials for compliance. Managing OTC switches and local regulatory strategies. Regulatory Compliance: Keeping product packaging and information up to date in line with current licenses. Implementing mandatory SOPs and ensuring regulatory compliance across the organization. Regulatory Environment Influence: Tracking and responding to emerging regulatory changes. Participating in local trade associations and influencing the regulatory landscape. Building relationships with health authorities to support the company's strategy. Innovation and Risk Management: Contributing to innovation programs and identifying regulatory risks. Overseeing the approval of risk management plans and related materials. About You:
A
university scientific degree
is required. Knowledge of
UK and international regulatory affairs
and
CHC regulations . Experience with regulatory aspects of medicines, food supplements, and medical devices. Strong
matrix team
working skills and ability to drive regulatory excellence. Additional language skills would be a plus. Company Culture and Benefits:
Sanofi highlights its commitment to progress, diversity, and inclusion, offering equal opportunities for all candidates. The role is based in
Reading
and offers a
hybrid work arrangement . This position plays a key role in ensuring Sanofi's products comply with regulations while influencing and shaping the regulatory landscape in the UK.
#J-18808-Ljbffr
