Regulatory Affairs Associate Review
at AstraZeneca
Degree Apprenticeship
Science
Cambridge
Review Submitted: April 2023
Overall Rating
5 /5
The Overall Rating is the average of all the ratings given in each category. We take those individual ratings and combine them into one final score!
5/5
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Overview of Role
5/5
-
Skills Development
5/5
-
Structure and Support
Overview of Role
Please give an overview of your role and what this involves on a day-to-day basis:
5/5
Expertly managed regulatory documents and systems, ensuring compliance with established procedures and regulatory requirements through efficient uploading and tracking.
• Strategically planned, prepared, and executed simple submissions, while providing support in the preparation and planning of regulatory dispatches.
• Acted as the primary liaison with Health Authority (HA) and its systems for designated regulatory tasks, including management of user fees, receipt of incoming FDA correspondence, ordering EudraCT number, EudraLink support, and use of HA portals.
• Assumed responsibility for ordering and tracking specific regulatory requirements, such as Registration samples, Certificates of Pharmaceutical Product, and Legal documentation, including Letters of Authorisation and Powers of Attorney, as well as translations of regulatory documentation.
• Offered support across the organization for assigned non-drug project roles and responsibilities, acting as a designated point of contact or superuser.
• Provided coaching, mentoring, and knowledge sharing within the Regulatory Affairs and Management (RAM) skill group.
• Contributed to process improvement initiatives for enhanced efficiency and effectiveness.
• Strategically planned, prepared, and executed simple submissions, while providing support in the preparation and planning of regulatory dispatches.
• Acted as the primary liaison with Health Authority (HA) and its systems for designated regulatory tasks, including management of user fees, receipt of incoming FDA correspondence, ordering EudraCT number, EudraLink support, and use of HA portals.
• Assumed responsibility for ordering and tracking specific regulatory requirements, such as Registration samples, Certificates of Pharmaceutical Product, and Legal documentation, including Letters of Authorisation and Powers of Attorney, as well as translations of regulatory documentation.
• Offered support across the organization for assigned non-drug project roles and responsibilities, acting as a designated point of contact or superuser.
• Provided coaching, mentoring, and knowledge sharing within the Regulatory Affairs and Management (RAM) skill group.
• Contributed to process improvement initiatives for enhanced efficiency and effectiveness.
To what extent do you enjoy your programme?
5/5
Skills Development
Have you learnt any new skills or developed existing skills?
5/5
Structure and Support
How well organised/structured is your programme?
5/5
How much support do you receive from your employer?
5/5
How much support do you receive from your training provider when working towards your qualifications?
5/5
How well do you feel that your qualification (through your training provider) helps you to perform better in your role?
5/5
Are there extra-curricular activities to get involved in at your work? (For example, any social activities, sports teams, or even professional networking events.)
5/5
Recommendations & Advice
Would you recommend AstraZeneca to a friend?
Yes
Why?
AstraZeneca is a company that invests in its employees are always provides opportunity for its employees to grow.
What tips or advice would you give to others applying to AstraZeneca?
To apply straight away to get started on a prosperous career with the company.
