Job Description
Industry/ Organization Type: Pharmaceutical Co
Position Title: Regulatory Affairs Specialist
Working Location: Chinatown (Hybrid)
Working Hours: Flexi-Hours
Salary Package: Basic up to $3,500 + Bonus
Duration: Permanent/Part-Time
Key Responsibilities
Prepare and submit regulatory documents, including pre-market submissions, to authorities to obtain required approvals.
Work with product development, quality assurance and marketing teams to develop regulatory strategies that support business plans.
Assist in preparing and maintaining regulatory files and product registrations for different markets.
Act as the main contact for regulatory authority queries and manage communication between authorities and internal stakeholders.
APPLY NOW!!!
Bachelor’s degree in Life Sciences, Regulatory Affairs or a related field.
Minimum 1 year of experience in regulatory affairs in the healthcare or pharmaceutical sector.
Good knowledge of relevant regulatory requirements and guidelines (e.g. FDA, EMA, ISO).
Strong analytical skills with the ability to understand and interpret complex regulatory documents and data.
Certification in Regulatory Affairs (e.g. RAC) is an advantage.
Familiar with project management tools and techniques to support timely regulatory submissions.
Kindly apply through ANY of the following methods:
Submit your application by clicking the APPLY button;
Email your resume to ************* Please indicate #81111 on the email subject.
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