Teva Pharmaceuticals Hiring b.sc, M.sc, B.Pharm, M.Pharm for Regulatory Affairs Associate II
Company
Info
Teva
is a global pharmaceutical leader and the world's largest generic medicines
producer, committed to improving health and increasing access to quality health
solutions worldwide. Our employees are at the core of our success, with
colleagues in over 80 countries delivering the world's largest medicine cabinet
to 200 million people every day. We offer a uniquely diverse portfolio of
products and solutions for patients and we've built a promising pipeline
centered around our core therapeutic areas. We are continually developing
patient-centric solutions and significantly growing both our generic and
specialty medicines business through investment in research and development,
marketing, business development and innovation. This is how we improve health
and enable people to live better, healthier lives. Join us on our journey of
growth!
Job
Description
- Prepare, compile,
review and submit high quality submissions for all required post-approval
activities in accordance with EU legislation and in-house standards.
- Responsibility for MA
compliance with both legislation and business needs.
- Prioritise, plan and
monitor submission for allocated procedures while documenting and
informing involved parties of progress.
- To give regulatory
support to project teams, stake holders and European Units for defined
product responsibilities.
- Support the development
and implementation of regulatory strategies for defined projects.
- Communicate with other
Teva departments across Europe and European Agencies regarding proposed
and pending submissions.
- Maintain and develop
awareness of current/pending regulatory legislation and guidelines.
- Support the defined
processes within the department and provide input where improvements can
be made.
Function
Regulatory
Affairs
Qualifications
- M Pharm/ MSc: 6+ years
of experience
- B Pharm/BSc: 6+ years
of experience
Join for Regular Job Updates in What's App & Telegram
No comments:
Post a Comment