Senior Regulatory Affairs Specialist

Date: Aug 4, 2025

Location:

Mongkok, Hong Kong, 122001

Company: Teva Pharmaceuticals

Job Id: 63197

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

A full-time position for Hong Kong to work on new submission / maintenance / labelling / regulatory compliance.

Collaborate with Quality, Supply Chain and Commercial Team.

Involvement in multinational regulatory issues and with concepts of regulatory strategy.

Ensure that all new products are registered according to local authority regulations and corporate policy as well as maintaining the MA of the existing products.

Ensure labeling (including local repackaging components) of all products introduced in the local market are compliant to local regulatory requirements and Corporate Guidelines.

Ensure that all changes in particulars and renewal of registered products as required by the local Health Authorities which are in compliance with corporate policy and the local Authorities’ regulations.

Collaborating with local partners in Macau comply with regulations on medicinal products.

How you’ll spend your day

New Product / Project Registration:

Coordinate and support technical and scientific regulatory activities
Communication with oversea counterpart for necessary dossiers and documents for submissions
Work with global RA and business partners of updating submission progress

Lifecycle Management:

Plan and manage product lifecycle changes
Coordinate and monitor artwork / packaging process of variation of existing products
Review and update Patient Information Leaflet in accordance with local regulatory requirements / company guideline

Business Support:

Provide regulatory support for commercial activities, e.g. registration information for tender submission
Review of marketing materials. Ensure promotional materials are complied with the requirements of Undesirable Medical Advertisement Ordinance (UMAO) and DoH registration guidelines

RA Processes:

Ensure that processes are clearly defined in SOPs for all critical tasks/duties e.g. regulatory filings, artwork, etc.
Establish and review local SOP/WIs
Maintain good record, databases, data of product registration and licenses per company guideline

Your experience and qualifications

Basic Degree in Life Sciences specialties, e.g. Pharmacy, Medicine, Biological Sciences
Preferably 2 or more years of regulatory experience in pharma and regulated industry
Experience in registration of medicinal products
Flexibility to work in a cross-cultural environment
Basic knowledge in drug development, pharmacovigilance, GxP processes, QA would be advantageous
A good balance of Regulatory and Business acumen
Solid knowledge and understanding of local drug / healthcare regulations and ability to apply them at work effectively
Good communication skills, fluent in written and spoken English in additional to local language to interact effectively with the government agencies in the country
Able to work under pressure and to tight timelines
Effective time management and multi-tasking
Flexibility in working schedule
Spontaneous team player and collaborator
Flair to simplify complex issues and manage project efficiently
Attention to details and logical analytical skills
Computer literacy
Demonstrated ability to handle competing priorities effectively
Results oriented, business-oriented and self-motivating
Openness to change and ability to think out of the box

Make a difference with Teva Pharmaceuticals

Please submit your CV and a cover letter responding to the selection criteria outlining relative keys skills and experience in relation to this role.

Please note that only shortlisted candidates will be contacted.

Reports To

Head of Regulatory Affairs, Hong Kong & Taiwan

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.