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Sr. RA Specialist @ AbbVie

KROnsiteFull-time
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About this role

Position: Sr. RA Specialist

Reports to: Regulatory Affairs Manager

Location: Seoul, South Korea

PRIMARY FUNCTION/OBJECTIVE

To manage the preparation of regulatory submissions of company products in order to obtain the necessary regulatory approvals and to provide regulatory input on regulatory matters to company personnel.

CORE JOB RESPONSIBILITIES

Developing RA strategies - assess timeline and lead development of regulatory strategy for new assets and line extensions based on the regulatory requirements as well as reflecting cross-functional team considerations. Support RA manager in developing regulatory strategies.Identifying and resolving regulatory issues and challenges that may arise during the product development, registration, or post-market phasesCollaborating with cross-functional teams, such as R&D, Quality Assurance, and Marketing, to gather necessary information and support regulatory affairs activities.Participating in problem-solving discussions and providing input on regulatory matters to support decision-making processes.Set up timelines on managing variations in accordance with strategyReviewing and evaluating product labeling, packaging, and promotional materials to ensure compliance with regulatory requirements.Conducting research on regulatory requirements and staying updated on changes in regulations and guidelines as Subject Matter ExpertsEvaluation of impact, implementation plan on the marketed products (hurdle, current situation) risk management, problem solvingProduct discontinuation/withdrawal/Marketing Authorization Transfer /co-promotion/co-marketing strategy reflecting feedback from internal stakeholders and global strategyConducting thorough reviews of contract terms and conditions to identify any regulatory implications or requirements that need to be addressed. PREFERRED QUALIFICATIONS

Education: Bachelors or equivalent degree in appropriate disciplineMore than 5 years’ experience in a regulatory position in pharma industryExperience in Oncology or Orphan Drug Designation preferredProficiency in both spoken and written EnglishStrong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making.Good interpersonal skills with the ability to communicate persuasively and with clarity, flexibility and adaptability to changing requirements, and creativity. Demonstrated proactive and positive team player.Drives continuous improvement and simplicity in process and approach and enhances agility. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Skills

OtherMid-Senior LevelPharmaceuticals

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