Regulatory Affairs Specialist
2 weeks ago
Regulatory Affairs Associate at Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic medicines, committed to making good health more accessible to millions around the world. As a global pharmaceutical company, we are currently seeking a highly skilled Regulatory Affairs Associate to support our European Generic new submissions.
As a Regulatory Affairs Associate, you will work closely with our Research and Development (R&D) colleagues to ensure that dossier technical content meets EU Regulatory data requirements for new Marketing Authorisation Applications. Your key responsibilities will include:
- Optimizing dossier content for submissions to regulatory authorities
- Performing regulatory activities from pre-submission to post-approval phases
- Communicating regulatory information to internal stakeholders and external partners
- Tracking and monitoring queries from regulatory authorities
- Ensuring compliance with departmental Standard Operating Procedures (SOPs)
The ideal candidate will possess a Pharmacy, Chemistry, or Life Sciences degree, with relevant regulatory affairs experience and knowledge of pharmaceutical processes and requirements. If you are a self-motivated, analytical individual who enjoys working in a collaborative team environment, this could be an excellent opportunity for you.
We offer a rewarding career with great benefits, including annual leave, flexible working arrangements, health insurance, and recognition programs. If you are looking to advance your career in regulatory affairs, we encourage you to apply.
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Regulatory Affairs Specialist
5 days ago
Harlow, Essex, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team at Teva Pharmaceuticals. As a key member of our EU Regulatory Affairs department, you will play a critical role in supporting the submission of new marketing authorization applications and post-approval variations for our generic medicines.Key...
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Regulatory Affairs Specialist
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Harlow, Essex, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team at Teva Pharmaceuticals. As a key member of our EU Regulatory Affairs department, you will play a critical role in supporting the submission of new marketing authorization applications and post-approval variations for our generic medicines.Key...
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Harlow, Essex, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team at Teva Pharmaceuticals. As a key member of our EU Regulatory Affairs department, you will play a critical role in supporting the submission of new marketing authorization applications and post-approval variations for our generic medicines.Key...
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Harlow, Essex, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled Regulatory Affairs Associate to join our team at Teva Pharmaceuticals. As a key member of our EU Regulatory Affairs department, you will play a critical role in supporting the submission of new marketing authorization applications and post-approval variations for our generic medicines.Key...
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Harlow, Essex, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly experienced and skilled Director, Regulatory Affairs CMC Combination Products to join our Global Regulatory Affairs, CMC Biologics, Devices department at Teva Pharmaceuticals.Key ResponsibilitiesProvide global regulatory CMC strategy and guidance for combination products, platform devices, and assigned marketed products,...
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Harlow, Essex, United Kingdom Teva Pharmaceuticals Full timeAbout the RoleWe are seeking a highly skilled and experienced Director, Regulatory Affairs CMC Combination Products to join our Global Regulatory Affairs, CMC Biologics, Devices department at Teva Pharmaceuticals.Key ResponsibilitiesProvide global regulatory CMC strategy and guidance for combination products, platform devices, and assigned marketed products,...
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