Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to:
- Career development with an international company where you can grow the career you dream of.
- Competitive remuneration package including good salary, bonus potential, package of benefits and continuous learning opportunities within an excellent multinational working environment.
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
For our Abbott Established Pharmaceuticals Division EPD we are currently looking for a Regulatory Affairs Associate to join our great team in Israel. This will be a temporary, maternity cover role, based on a fixed-term employment contract. The position will be located in our office in Tel-Aviv.
Regulatory Affairs Associate supports the regulatory team in handling the registration of company’s products, fulfils national regulatory authority regulations and Abbott Laboratories policies, procedures and regulations, on both local and international level.
RA Associate complies with the company’s policies and procedures, local regulation/legislation requirements to meet statutory, quality and business requirements within the overall strategy and objectives of Abbott Laboratories Ltd. and Israeli MoH.
What You'll do:
- Support the company portfolio and provide regulatory guidance and support to internal groups in line with local, regional and global strategies while ensuring alignment and collaboration across Abbott.
- Help maintaining product marketing authorizations including regulatory authority approvals for various regulatory activities as required.
- Prepare and submit regulatory applications required in the product life cycle.
- Review and provide regulatory assessment for variations.
- Follow up of mandatory requirements for registration.
- Interact with local, regional and global personnel on regulatory issues.
- Communicate information and present status updates on product/project activities to key internal/external stakeholders.
- Maintain professional knowledge and keep abreast of the legislation and highlight the potential impact on the business.
- Ensure compliance with statutory obligations.
Required qualifications and background:
- University degree in a related field (pharmacy, chemistry, chemical engineering or similar preferred).
- At least 2 years experience in regulatory in pharmaceutical industry.
- Mastery of relevant regulations and the ability to stay abreast of pertinent regulations, knowledge and experience of GDP and GMP.
- Fluent in English and Hebrew
- Team-player with strong organizational skills, high ethical standards and ability to prioritize tasks.
- Strong interpersonal skills and can-do attitude would be highly desirable.
- Ability to work full-time (part time is also acceptable, but not less than 80%).
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
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