Regulatory Affairs Associate I

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity

The Regulatory Affairs Associate I is responsible for the publishing and dispatch of basic lifecycle management submissions and troubleshooting document issues.  The Regulatory Affairs Associate I follows defined standards and works in close collaboration with senior staff and operational team members to ensure the creation of accurate, timely and technically competent regulatory submissions.

 

Domestic travel: up to 10% 

Location: Parsippany, New Jersey (100% on-site)
 

How you’ll spend your day

• Build and dispatch lifecycle management submissions   
• Troubleshoot document issues with Adobe Acrobat & MS Word    
• Manage technical aspects for assigned submissions and status updates to concerned parties.    
• Collaborate with scientific personnel for planning, preparation, publishing and quality control checks of submissions.   
• Support submission efforts in other business units.    
• Maintain working knowledge of internal and external publishing standards  
• Identify when data seems incorrect, incomplete or needs verification. (Understand the business benefit and risk to steps being performed. Understand why steps are taken and can relate them to business objectives.)
• Check work to ensure accuracy and completeness.
• Identify existing problems/process inefficiencies and have novel approaches to solving problems. (Contribute original and resourceful ideas in brainstorming sessions.)
• Describe customers’ business and expectations. (Show interest in, anticipate, and respond to customer needs in a timely manner.)

Your experience and qualifications

• Bachelors Degree required, preferably in Life Sciences or Information Technology
• Microsoft Office and Adobe Acrobat experience required

 

This is an entry level position.  No experience is needed but there is a strong preference for Regulatory Operations/Regulatory Affairs experience. 

Enjoy a more rewarding choice

We offer a competitive benefits package, including Medical, Dental, Vision, and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 13 paid Holidays, 6% match on the 401(k), Employee Stock Purchase Plan, and Tuition Assistance. 

Already Working @TEVA?

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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. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

 

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