Regulatory Affairs Associate III

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

Responsible for driving all the activities independently pertaining to Regulatory Affairs of assigned project for Solid Oral Dosage forms.

How You’ll Spend Your Day

• Independently compile high-quality CMC (m2 & m3) dossier and review the compilation of peers for new registration, query responses to review letters from agency and post approval supplements (on need basis) for EU in CTD format as per the submission timelines.
• Additional support leveraging dossiers for International Market regions.
• Assist submissions team with CMC related m1 administrative documentation
• Provide strategic input and regulatory intelligence to allotted R&D projects, including cross-functional initiatives
• Effective supervision and coaching of peers/ junior team members
• Support due diligence process pre-filing and implement action plan to address deficiencies
• Assess submission documentation in consideration and compliance with the regulatory requirements and to provide inputs to cross functional teams.
• Coordinate (on need basis) with external parties and cross functional teams to obtain essential scientific data and documents required for regulatory submissions
• Escalate key issues to management (risk of delays to submissions, risk to approvability, complex supporting data requirements)
• To deputize for Manager during his/her absence
  
  

Your Experience And Qualifications

Qualification: Graduation/ Post graduation in Science/ Pharma discipline

Desired Experience

• Minimum 6+ Yrs (for post-graduates)/ 8+ Yrs (for graduates) in core pre-approval regulatory activity in EU and allied markets for Solid Oral Dosage forms. Preference for additional experience in formulation/ analytical development.
• Regulatory knowledge throughout new development & product lifecycle with substantial experience with various products and on different Markets.
  
  

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas 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.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Tevas policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

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