Senior Regulatory Affairs Professional

2 weeks ago

Singapore beBeeRegulatoryAffairs Full time
Job Description

We are seeking a highly skilled Regulatory Affairs Specialist to support our local and SEA country submissions for new registrations, product renewals, variations, and clinical trials. The successful candidate will ensure regulatory compliance with internal and external requirements, including the Singapore Health Products Act and Health Sciences Authority guidance.

Key Responsibilities
  • Spearhead local/SEA country submission processes for new registrations, product renewals, variations, and clinical trials.
  • Ensure timely and accurate submissions to relevant regulatory authorities.
  • Maintain up-to-date knowledge of regulatory requirements and guidelines.
  • Collaborate with cross-functional teams to achieve regulatory objectives.
Required Skills and Qualifications

To succeed in this role, you will need:

  • A degree in a relevant field (e.g., Life Sciences, Pharmacy, or Law).
  • Proven experience in regulatory affairs, preferably in the pharmaceutical industry.
  • Excellent communication and project management skills.
  • Ability to work independently and as part of a team.
Benefits

As a valued member of our team, you can expect:

  • A competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • A dynamic and supportive work environment.
Other Information

We promote global participation in clinical trials, guided by our core values of passion, innovation, urgency, accountability, inclusion, and integrity. We prioritize the health and safety of our staff, customers, patients, and communities. If you reside in or plan to work from Los Angeles County, please review additional information at this link.

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