Teva Pharmaceuticals Hiring for Regulatory Affairs Associate III – 1436 at Navi Mumbai, India Full Time

Regulatory Affairs Associate III – 1436

Date: Jul 8, 2022

Location: Navi Mumbai, IN, 400706

Company: Teva Pharmaceuticals

Who are we?

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

• Review and submit high quality submissions for all required post-approval activities in accordance with US current regulations, guidelines/ updates and in-house standards.

• Support the development and implementation of regulatory strategies for defined projects.

• Co-ordinate regulatory resource to projects, provide technical regulatory support to individual projects.

• To give regulatory support to project teams, stakeholders and US RA team for defined product responsibilities.

• Effective supervision and coaching of reporting regulatory professionals and administrative support staff, providing support in day to day work and long term development.

• Prioritise, plan and monitor submission for allocated procedures while documenting and informing involved parties of progress.

• Communicate with other Teva departments across US regarding submissions.

• Maintain and develop awareness of current US regulatory guidelines.

Qualifications

• M Pharm/ MSc: 9+ years of experience

• B Pharm/BSc: 10 years of experience

Function

Regulatory Affairs

Sub Function

Medical Regulatory Affairs

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on “Employee Central”. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site (https://performancemanager.successfactors.eu/sf/careers/jobsearch?bplte_company=1080030P)

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva’s global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

EOE including disability/veteran