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Regulatory Affairs Senior Associate - West Yorkshire, United Kingdom - Michael Page (UK)
Description
This organisation is a leader in the Pharmaceutical industry with a substantial presence.Employing over 1,000 dedicated professionals, the company is known for its commitment to research and development, producing high-quality pharmaceutical products that enhance and save lives.
Assist in Regulatory activities including management of applications for new marketing authorisations as per local laws and regulations.Develop and implement regulatory strategies for new and existing products.
Prepare and submit regulatory documents to health authorities.
Collaborate with internal teams to ensure compliance with applicable regulations and standards.
Review and approve variations strategies and documentation to ensure compliance for existing marketing authorisations.
Maintain regulatory systems providing timely notifications to stakeholders to ensure compliance and supporting product launch goal.
Support with regulatory training to internal teams.
A successful Senior Regulatory Affairs Associate should have:
~ A degree in Life Sciences or related field.
~2+ years experience in regulatory affairs within the life science industry.
~ Technical knowledge of pharmaceutical regulations and guidelines.
~ A proactive attitude towards continuous learning and development.
Competitive Salary.
Generous holiday leave of 25 days plus bank holidays.
A rewarding pension scheme.
Comprehensive health cash plan.
A comprehensive rewards and wellbeing programme.
Free onsite parking.
Join our clients team and take the next step in your career as a Senior Regulatory Affairs Associate in the life science industry.