
Assoc. Spclst., Regulatory Affairs (Pharmacy Intern)
- Hong Kong
- Permanent
- Full-time
- Regulatory Affairs – To handle New Product Registration and product Registration Life-Cycle Management, with strategic planning for new launch and/or implementation of post-approval variation; Provide support to cross-functional teams such as Tender and In-Market Quality support.
- Medical Affairs – To handle inquiry & patient program, experience to visit with HCP & symposium.
- Pharmacovigilance – To handle AE reporting & if there is a need, to verify the data.
- Others – Attending Drug Office seminar and/or Medical Device seminar, opportunities to work with different stakeholders, e.g. DOH officers, CPO, Legal Advisor etc.
- Currently pursuing a Bachelor of Pharmacy ("BPharm") Programs offered by The University of Hong Kong ("HKU") and The Chinese University of Hong Kong ("CUHK").
- Demonstrate proficiency with PowerPoint, Word, Excel, and other Office365 products and should be sufficiently IT savvy to learn new systems
- An excellent team player who is able to readily take on responsibilities and work independently
- Excellent verbal, written communication and documentation skills
- Have a positive, proactive, can-do attitude and a keen learner
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.Employee Status: Intern/Co-op (Fixed Term)Relocation:VISA Sponsorship:Travel Requirements:Flexible Work Arrangements: Not ApplicableShift:Valid Driving License:Hazardous Material(s):Required Skills: Adverse Event Report, Adverse Event Report, Audits Compliance, Business, Collaborative Development, Communication Management, Data Quality Assurance, Document Control Systems, Electronic Common Technical Document (eCTD), Employee Training Programs, Healthcare Innovation, Management Process, Medical Affairs, Medical Devices, Pharmacy Laws, Policy Implementation, Product Lifecycle, Product Registrations, Records Retention Management, Regulatory Affairs Compliance, Regulatory Applications, Regulatory Communications, Regulatory Compliance, Regulatory Compliance Audits, Regulatory Strategy Development {+ 3 more}Preferred Skills:Job Posting End Date: 10/30/2025*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.