Teva Pharmaceuticals Hiring! Apply Now for Regulatory Affairs Associate Role
About Teva Pharmaceuticals
Teva Pharmaceuticals is a leading global pharmaceutical company committed to improving the health and well-being of people worldwide. With a focus on developing innovative generics and specialty medicines, Teva is dedicated to ensuring patient access to high-quality treatments.
Job Title: Regulatory Affairs Associate – EU – Generics
Location: Harlow, England, United Kingdom
A Day in the Life of a Regulatory Affairs Associate…
On a daily basis, with support from your line manager, you will be working cross-functionally with R&D colleagues to:
Key Responsibilities:
- Ensure dossier technical content is optimal and aligned with EU Regulatory data requirements for new EU Marketing Authorisation Applications and post approval variations, where required
- Perform necessary regulatory activities for assigned projects from pre-submission until post-approval handover to regulatory maintenance teams
- Communicate regulatory information for assigned projects before, during and after approval
- Track and monitor queries/deficiency letters/commitments from/to European Health Authorities
- Ensure compliance with departmental and company SOPs
Through training and on-the-job experience, you will develop and grow your understanding of the European regulatory environment and supporting data requirements.
Who we are looking for
Do you have…?
- Pharmacy/Chemistry or Life Sciences degree
- Regulatory Affairs experience ideally with medicines, medical devices, OTCs
- Knowledge of pharmaceutical & scientific processes, regulatory requirements, and internal/external communications
- Good attention to detail and time management skills
If you have the drive and skills to excel in the field of regulatory affairs, we encourage you to apply for this exciting opportunity with Teva Pharmaceuticals.
Apply for this position here
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