Regulatory Affairs Associate: Global Submissions Lead (Travel)

Kyowa Kirin International; Galashiels; On-site; GBP 30,000 - 40,000; Full time

Job summary

A global pharmaceutical company is seeking a Regulatory Affairs Associate in Galashiels, Scotland. This role involves supporting regulatory submissions and collaborating with cross-functional teams to enhance product lifecycle management. Ideal candidates will hold a life science qualification and have experience in regulatory affairs. Strong communication, organizational skills, and an ability to manage regulatory timelines are essential. This position offers the opportunity to contribute to impactful projects in a dynamic environment.

Qualifications

• Experience in pharmaceutical regulatory affairs.
• Ability to travel locally and internationally.
• Flexibility of working hours.

Responsibilities

• Support creation of regulatory submission strategy.
• Collaborate with cross-functional departments.
• Execute regional regulatory strategy.
• Lead/manage regulatory submissions.
• Ensure maintenance of marketing authorisations.
• Manage regulatory timelines and activities.
• Ensure compliance with relevant legislation.

Skills

Communication skills

Organisational skills

Negotiation skills

Attention to detail

Education

Life science qualification

Job description

A global pharmaceutical company is seeking a Regulatory Affairs Associate in Galashiels, Scotland. This role involves supporting regulatory submissions and collaborating with cross-functional teams to enhance product lifecycle management. Ideal candidates will hold a life science qualification and have experience in regulatory affairs. Strong communication, organizational skills, and an ability to manage regulatory timelines are essential. This position offers the opportunity to contribute to impactful projects in a dynamic environment.