Regulatory Affairs Associate - III

Regulatory Affairs Specialist

Specific

Job Responsibilities:

• Responsible for the preparation of moderately complex regulatory submissions which require interaction with departments outside of Regulatory Affairs CMC for investigational products for the US, Asia and LATAM and marketed products for the US in line with ICH requirements, regional requirements and scientific and company policies and procedures.
• Responsible for routine clinical and commercial labeling approvals and changes, protocol reviews, drug listing review and ensure ensuring product packaging and associated information is updated and maintained in accordance with the product license.
• Develop and maintain knowledge of regulatory requirements independently and with the line manager.
• Assess change controls for regional regulatory impact and record assessment using a variety of internal systems.
• Contribute to local process improvements, which have an impact on the working of the RA CMC function or other departments.
• Work cross-functionally within a matrixed organization.
• Primarily plans, schedules and arranges own activities in alignment with project goals and deadlines.
• Must be capable of leading a small team in the preparation of regional submissions.
• Must work well under deadlines and have excellent attention to detail. Strong computer and organizational skills are required. Work is performed under the limited direction of a senior Regulatory Affairs professional.
• Excellent verbal and written communication skills and interpersonal skills are required.

Education & Experience:

• A Bachelor’s Degree with a minimum of 6+ years of relevant training or industry experience preferably in a GMP environment, or a Master’s Degree with a minimum of 4+ years of relevant training or industry experience preferably in a GMP environment.
• Degree in a relevant scientific field.
• Relevant Regulatory CMC submission experience.
• Regulatory Affairs Certification (RAC).