About this role
Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story.
We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee.
At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.
Main Responsibilities
Pharmacovigilance (PV) / Post‑Marketing Surveillance (PMS) Support
- Support PV and PMS activities in alignment with local and global requirements
- Assist in the management of PMS activities, including planning, coordination, and execution of project deliverables
- Provide PMS‑related communication to key internal and external stakeholders
- Coordinate PMS IRB review schedules and payment processes
- Maintain and organize PMS documentation in accordance with applicable requirements
- Support vigilance case processing and case management activities
- Prepare and submit regular and expedited PV reports, as required
- Support SOP updates, revisions, and gap analysis activities
- Assist with Safety Data Exchange Agreement (SDEA) and Vigilance Procedure (VP) management
- Maintain a local vigilance system and ensure appropriate handling of safety information
- Support and maintain a 24/7 local vigilance coverage system
- Ensure local vigilance records and files are kept accurate and up to date in line with company procedures and local regulations
- Perform screening of local medical and medical device literature to identify potential case reports related to products
- Track completion of PV training activities
- Maintain and monitor a local vigilance generic email inbox to facilitate safety information exchange
- Support PV and vigilance audits and inspections
- Monitor and report regulatory intelligence relevant to PV and PMS
Other Team Administration Responsibilities (as required)
- Support billing and invoice‑related processes
- Provide contract administration support
- Assist with GxP document management and archiving
Education
- Bachelor’s degree in Pharmacy, Nursing, Life Sciences, or a related discipline
Work Experience
- Minimum of three years’ experience in the pharmaceutical, biotechnology, or consumer healthcare industry
- Demonstrated interest in product safety and/or post‑marketing surveillance
Required Skills and Experience
- Ability to work effectively both independently and collaboratively within a team environment
- Strong time‑management skills with the ability to work under tight deadlines
- High level of accuracy and attention to detail
- Strong verbal, written, and interpersonal communication skills
- Effective problem‑solving and influencing capabilities
- Proficiency in written and spoken English
- Strong working knowledge of Microsoft Office applications
- Clear, proactive, and effective communication style
* 국가유공자 등 예우 및 지원에 관한 법률에 따른 보훈대상자 및 장애인고용촉진 및 직업재활법에 따른 장애인은 관련 법령에 따라 우대합니다. (해당 시 관련 증빙서류 제출 필수)
In accordance with applicable laws, preference is given to veterans and persons with disabilities. Candidates qualifying for these preferences are required to submit relevant certificates and supporting documentation during the application process.
About Galderma
Global dermatology company specializing in aesthetic, consumer, and prescription skin care treatments. Headquartered in Zug, Switzerland.
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