Regulatory Affairs Associate

Jobsinkent; Folkestone; Híbrido; CAD 66.000 - 90.000; Jornada completa

Descripción de la vacante

Jobsinkent is seeking a Regulatory Affairs Associate to join the Global Markets team on a temporary long-term contract, supporting regulatory compliance and product registrations across EMEA. The role involves coordinating submissions, maintaining licences and working with internal teams and external authorities to ensure timely market access.

The position requires strong organisation, attention to detail and excellent communication skills to manage multiple regulatory projects in a

Formación

• Understanding of EU MDR 2017/745 and regulatory requirements.
• Ability to manage multiple regulatory projects concurrently.
• Experience supporting product registrations across international markets.

Responsabilidades

• Support regulatory enquiries and registration activities for products.
• Prepare and coordinate documentation for new registrations and licence maintenance.
• Research regulatory requirements across EMEA and apply them to submissions.
• Collaborate with Quality, R&D, Marketing, Supply Chain and Legal to assemble dossiers.
• Manage project timelines and ensure timely submissions and approvals.
• Coordinate regulatory notifications and distributor/regulator submissions.
• Maintain regulatory records and electronic files.

Conocimientos

Regulatory project management

Attention to detail

Written and verbal communication

Stakeholder management

Proactive and self-motivated

Analytical thinking

MS Office proficiency

Herramientas

Microsoft Office

Descripción del empleo

Location: Folkestone, Kent – Hybrid Working
Contract: Temporary long term
Sector: Medical Devices / Consumer Healthcare / Regulatory Affairs

The Opportunity

My client is seeking a Regulatory Affairs Associate to join their Global Markets team on a temporary contract basis, supporting regulatory compliance and product registrations across Europe, the Middle East and Africa (EMEA).

This is an excellent opportunity to join an established international organisation and gain broad exposure across Medical Devices, Medicines and Food Supplements.

The successful candidate will play an important role in supporting new product registrations, maintaining existing licences and coordinating regulatory activities across multiple international markets. You will work closely with internal stakeholders, regulatory authorities and distributor partners to help ensure products remain compliant and can be successfully brought to market.

The position would suit a highly organised and detail-focused regulatory professional who is comfortable managing multiple projects and working across different regulatory frameworks.

Key Responsibilities

• Support commercial teams, distributors and internal stakeholders with regulatory enquiries and product registration activities.
• Prepare, coordinate and submit documentation for new product registrations and the maintenance of existing licences.
• Research, interpret and apply regulatory requirements across EMEA markets.
• Work cross-functionally with teams including Quality, R&D, Marketing, Supply Chain and Legal to compile and maintain technical documentation and regulatory dossiers.
• Manage registration projects and ensure submissions and approvals progress in line with agreed timelines.
• Monitor product changes and coordinate any necessary regulatory notifications or submissions to distributors and regulatory authorities.
• Prepare and coordinate the signing, legalisation and authentication of regulatory documentation.
• Maintain accurate records of registrations, licences and submissions within internal regulatory databases and systems.
• Organise and maintain electronic regulatory files in accordance with internal procedures.
• Liaise with distributors, regulatory authorities, trade associations and other external stakeholders to support market access.
• Produce reports and provide updates on registration status, compliance activities and project milestones.
• Support continuous improvement initiatives across regulatory processes and ways of working.
• Provide general administrative support to the wider Regulatory Affairs team as required.

About You

Essential

• Good understanding of EU Medical Device Regulation (EU MDR 2017/745) and associated regulatory requirements.
• Strong organisational and project management skills, with the ability to manage multiple priorities simultaneously.
• Excellent attention to detail and a commitment to accuracy.
• Strong written and verbal communication skills.
• Ability to build effective relationships with internal and external stakeholders.
• Proactive and self-motivated approach, with the confidence to work independently and use initiative.
• Strong analytical and problem-solving skills.
• Proficiency in Microsoft Office, including Word, Excel, Teams and SharePoint.

Desirable

• Previous experience within Regulatory Affairs, Product Registrations, Compliance or a related discipline.
• Experience supporting registrations for Medical Devices, Medicines, Food Supplements or Consumer Healthcare products.
• Knowledge or experience of regulatory requirements across Europe, the Middle East and Africa.

What's on Offer

This temporary position provides an excellent opportunity to work within a global Regulatory Affairs environment, with exposure to a broad portfolio of products and international markets.

You will benefit from a hybrid working arrangement, a collaborative team environment and the opportunity to further develop your international regulatory experience.

If you have experience within Regulatory Affairs and are looking for your next opportunity within a varied, internationally focused role, we would be keen to hear from you.