Regulatory Affairs Associate II at Teva Pharmaceutical Industries Ltd. - Israel

, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

11 Jun, 26

Salary

0.0

Posted On

13 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Affairs, European Market RA, Regulatory Documentation, Coordination, Planning, Monitoring, IT Systems Maintenance, Health Authority Communication, Guidance, Legislation Awareness

Industry

Pharmaceutical Manufacturing

Description

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.The opportunity Providing regulatory support for European Market RA. Coordination of assigned regulatory activities. How you’ll spend your day Completion of designated projects and tasks supporting European Market RA, according to internal Work Instructions, with moderate level of guidance and direction by the manager. Coordination, prioritization, planning and monitoring the tasks related to assigned regulatory activities. Development/maintenance of the expertise and solving straightforward problems, related to assigned regulatory activities. Maintaining related documentation and regulatory IT systems, in line with internal procedures. Communication with Teva units across Europe Markets, with 3rd Parties and with related Health Authorities. Guiding and supporting more junior team members. Fulfilling other allocated department duties and ad-hoc tasks as directed by senior regulatory affairs staff. Completion of trainings assigned in Teva internal learning management system within defined timeframes. Attending team meetings and providing regular updates on the assigned activities and tasks to the manager. Maintaining and developing awareness of the current/pending regulatory legislation and guidelines Your experience and qualifications Qualifications: Masters in Pharmacy or Masters in Science/Life Sciences. College or University degree or equivalent work experience that provide knowledge of and exposure to fundamental theories, principles and concepts. Experience: 4-6 years of experience in the Pharmaceutical Industry, ideally within Regulatory Affairs but R&D, Development or QA would be considered. Experience of regulatory documentation within Europe Markets. How We’ll Take Care of You  At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community. When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.  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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Responsibilities

The role involves providing regulatory support for the European Market RA, which includes coordinating, prioritizing, and monitoring assigned regulatory activities according to internal procedures. Responsibilities also cover maintaining documentation, communicating with various stakeholders including Health Authorities, and guiding junior team members.