Job Information
J&J Family of Companies Senior Regulatory Affairs Specialist in Singapore, Singapore
Senior Regulatory Affairs Specialist - 2406182708W
Description
At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity. Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world. When You Join Johnson & Johnson, Your Next Move Could Mean Our Next Breakthrough. Are you highly motivated and striving to make an impact? We invite you to learn more about our Regulatory Affairs Team at the Johnson & Johnson Family of Companies!
The Senior Regulatory Affairs Specialist is a member of the local Regulatory Affairs Team (Innovative Medicine) supporting the Regulatory Affairs Lead, Singapore in executing regulatory strategies and maintaining compliance to internal, external regulations and Quality Management System.
Overall purpose of job:
Coordinates, compiles, and submits new drug applications (NDAs), product line extensions and variations to Health Authority.
Ensure compliance to company SOPs and Quality Management System.
Essential duties and responsibilities:
Ensure timely product registrations by internal timelines
Prepare and maintain existing product licenses with updated CMC and CCDS changes
Gathers and assembles information necessary for submission in accordance with regulations and relevant guidelines
Prepare responses to regulatory agencies’ questions and other correspondences, in collaboration with local and global functional teams
Interact with regulatory agency personnel in order to expedite approval of pending applications and to resolve regulatory matters
Collaborate with management and internal stakeholders (e.g. Medical Affairs, Marketing) to manage product strategy, local registration and launch activities. Align filing plans and timelines with internal stakeholders including management, business partners and regional office
Ensure adherence to standard operating procedures and protocol for the timely approval of marketed drugs
Ensure compliance to J&J and local regulatory guidelines
Provide ad-hoc local assessment on regulatory filings
Provide regulatory support to other countries when required e.g. CPP application
Manage and maintain local and global regulatory tracking systems
Ensure post-approval commitments by the health authority are managed in a compliant manner
Assist in the review of labeling and promotional materials
Participate in internal and external audits
Maintenance of the relevant company regulatory licences (e.g. Therapeutic Products’ Importer & Wholesaler Licences, Controlled Drug Wholesale Licence), where applicable
To act as the Company’s Responsible Person, with the authority to hold the specific licenses required for the legal function of the business with the health authority.
To act as Company’s Controlled Substances Responsible Person.
Qualifications
Essential knowledge and skills:
Bachelor's degree or equivalent in Pharmacy, Science or related discipline;
Minimum 2 – 3 years of experience in regulatory affairs within the pharmaceutical industry
Excellent verbal and written communication skills - proficiency in written and oral English is required;
Must be able to develop and maintain excellent working relationships, work successfully within a team environment and as an individual contributor;
Proactive team player, able to take charge and follow-through;
Proficiency with Microsoft applications such as Excel, Word, PowerPoint.
Core competencies required for this role:
Excellent interpersonal & communication skills
Demonstrate strong planning, organizational and decision-making skills
Good team-player with strong collaborative mindset with cross-functional team and stakeholders
Meticulous, strong analytical and problem-solving skills
Results oriented with high sense of urgency
High integrity, ethical and professional
Independent, self-driven and change agent
Coaching and mentoring of junior team members, where applicable
Primary Location Asia Pacific-Singapore-Singapore-Singapore
Organization Johnson & Johnson International (Singapore) Pte Ltd (8438)
Travel No
Job Function Regulatory Affairs
Req ID: 2406182708W
J&J Family of Companies
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