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Galderma

Independent dermatology company delivering skincare therapies

Head of Regulatory Affairs

Full-TimeUpdated on 10/23/2026
No salary listed
Expert
Bachelor's
Tokyo, Japan
In Person
Biology & BiotechRegulatory & Quality (Life Sciences)

About the job

Requirements
  • A bachelor's degree or above in Pharmacy, Life Sciences, Engineering, or a related discipline.
  • A minimum of 10 years of Regulatory Affairs experience in the medical device or pharmaceutical industries.
  • Experience developing regulatory strategies, managing product registrations, and supporting lifecycle management in the medical device sector.
  • Experience working in a global or matrix organization.
  • Strong knowledge of Japanese regulatory requirements and approval processes for medical devices and pharmaceuticals.
  • Experience leading or making significant contributions to product registrations from submission through approval.
  • Experience interacting with regulatory authorities, including MHLW, PMDA, and TMG.
  • Working knowledge of Quality Management Systems (QMS), quality, and safety requirements, and experience partnering effectively across functions.
  • Experience leading and developing small teams.
  • Business-level written and spoken proficiency in English and Japanese.
  • Understanding of commercial drivers in healthcare, particularly consumer health products, and ability to provide advice that considers them.
  • Analytical skills and attention to detail, with the ability to define issues, questions, and data and propose solutions with appropriate urgency.
  • Communication skills and the ability to foster working relationships with internal and external stakeholders, including health authorities and industry associations.
  • Project management, problem-solving, presentation, time-management, negotiation, and interpersonal skills.
  • Ability to work independently in a hands-on capacity or as part of a team.
  • Ability to balance commercial needs with compliance requirements.
  • Ability to think strategically and innovatively to resolve regulatory issues and set strategic priorities.
  • Commitment to continued improvement in functional processes and performance.
  • Ability to contribute proactively to a productive work environment and deliver results.
  • Integrity and credibility.
  • Ability to combine strategic thinking with hands-on execution and lead by example.
  • Ability to communicate and promote understanding of QMS and regulatory requirements across the organization.
  • Ability to build trust and collaborate effectively with diverse stakeholders.
  • Open, transparent, and constructive communication style.
  • Adaptability and resilience in a fast-paced, evolving business environment.
Responsibilities
  • Serve as a key member of the Japan Leadership Team, contributing regulatory expertise to business and organizational decisions and supporting business and people objectives.
  • Fulfill the legally designated Marketing Authorization Holder General Manager (Sokatsu) responsibilities under applicable Japanese regulations.
  • Lead development and execution of regulatory strategies in Japan, ensuring compliance, risk management, and successful product registrations.
  • Oversee regulatory operations, including license maintenance and vigilance-system oversight, to ensure product safety and regulatory compliance.
  • Partner with local and global stakeholders to promote understanding of Japan-specific regulatory requirements and align regulatory and business strategies.
  • Lead and develop Regulatory Affairs, Quality, and Vigilance functions through people development, coaching, and organizational capability building while remaining involved in day-to-day regulatory activities.
  • Provide strategic regulatory advice and guidance to Japan leadership.
  • Take accountability for project objectives, aligning regulatory strategies with business priorities while participating in operational activities.
  • Lead Japanese regulatory strategy development and execution and provide recommendations on requirements, timelines, and feasibility.
  • Support day-to-day regulatory operations to meet business needs.
  • Lead regulatory submissions, including new registrations and change applications, and manage health-authority interactions.
  • Maintain marketed-product compliance through lifecycle activities, including change control, license maintenance, and labeling updates.
  • Identify lifecycle regulatory risks and challenges and work cross-functionally to develop solutions.
  • Review and approve promotional and non-promotional materials, including product labeling, for compliance with regulations, industry codes, and company policies.
  • Communicate regulatory application and product-change status to local and global stakeholders in a timely manner.
  • Evaluate and update product labeling to support compliance, commercial competitiveness, and timely product launches.
  • Maintain regulatory documentation, records, and databases, including Regulatory Information Management Systems (RIMS).
  • Maintain required business licenses and import permits.
  • Develop and implement local standard operating procedures (SOPs), work instructions, and processes to bridge gaps between global policies and local requirements.
  • Implement global regulatory SOPs and mandatory training requirements locally.
  • Monitor regulatory developments, legislative changes, industry trends, and competitor activities and incorporate relevant insights into regulatory strategies.
  • Support new-product introduction and launch with cross-functional teams.
  • Build and maintain relationships with external stakeholders, including MHLW, PMDA, TMG, consultants, and distributors.
  • Support regulatory inspections, audits, and assessments by health authorities and certification bodies.
  • Support post-market activities as needed.
  • Lead the company compliance program and promote adherence to global guidelines and local laws and regulations.
  • Foster an organizational culture of integrity, ethics, and compliance.
  • Monitor compliance with internal standards and applicable regulations governing interactions with healthcare professionals.
  • Oversee the local vigilance system in accordance with global SOPs, third-party agreements, and local regulatory requirements.
  • Review and approve local vigilance SOPs and supporting documentation.
  • Act as Deputy Local Safety Officer and support 24/7 vigilance coverage.
  • Ensure readiness for vigilance inspections and audits and support inspection activities as a key local contact.
  • Lead, coach, develop, and motivate Regulatory Affairs, Quality, and Vigilance team members.
  • Foster collaborative working relationships across functions.
  • Represent the company in industry associations, working groups, or professional committees when required.
  • Partner with corporate functions on trademark management and trade compliance matters.
  • Manage corrective and preventive action (CAPA) processes for compliance issues through completion.
  • Comply with applicable laws, regulations, the Galderma Code of Ethics, company policies, and SOPs.
Desired Qualifications
  • A valid pharmacist license in Japan.
  • Experience in the cosmetics sector.
  • Experience in aesthetics, dermatology, or related healthcare sectors.

About the company

Dermatology-focused medicines and skincare products are Galderma’s core business, including prescription therapies, over-the-counter skincare, and injectable aesthetics. It combines pharmaceutical R&D with consumer skin insights to develop treatments that address skin conditions, improve appearance, and support overall skin health. Unlike many peers, Galderma operates as an independent, publicly traded dermatology specialist with a long history in skin science, spanning prescription, OTC, and aesthetic segments. Its goal is to be a global leader in science-based solutions for skin conditions, growing across therapeutic dermatology, injectables, and skincare worldwide.

Company Size

1,001-5,000

Company Stage

Private

Total Funding

$5.7B

Headquarters

Lausanne, Switzerland

Founded

1981

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Simplify's Take

What believers are saying

  • H1 2026 sales hit $3.134 billion, up 24.6%, and guidance rose to 19-21%.
  • Galderma opened Miami headquarters in August 2026, targeting 200 staff and stronger U.S. selling.
  • The $650 million U.S. manufacturing buildout through 2030 supports supply and tariff resilience.

What critics are saying

  • FDA's July 1, 2026 Relfydess CRL pushes U.S. launch toward 2027.
  • AbbVie's Allergan Aesthetics still dominates Botox and Juvéderm, keeping Galderma behind.
  • Nemluvio and Relfydess depend on execution in the U.S.; another regulatory miss crushes momentum.

What makes Galderma unique

  • Relfydess, approved in 33 markets by July 2026, gives Galderma a proprietary neuromodulator.
  • Galderma spans Cetaphil, Restylane, Sculptra, Nemluvio, and Dysport across dermatology categories.
  • The September 21, 2026 SMI inclusion validates its scale and Swiss capital-market credibility.

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Benefits

  • Flexible Work Hours

Growth & Insights and Company News

6 month growth

0%

1 year growth

-1%

2 year growth

-1%
Yahoo Finance
Oct 23rd, 2026
China approves Galderma's Relfydess, first ready-to-use liquid neuromodulator, for frown lines

Galderma's Relfydess has won approval in China for the temporary improvement of moderate-to-severe frown lines in adults, the Swiss company announced on October 23, 2026. The country's National Medical Products Administration (NMPA) cleared the product, which Galderma calls the first and only ready-to-use liquid neuromodulator. Approval rests on a local phase III trial in China and the global READY trials, which had more than 2,300 participants. In the China study, 72.4% of patients saw a at least two-grade improvement at month one, against 1.6% on placebo. In READY-1, 39% reported improvement from day one, and up to 75% kept results for six months. Relfydess is now authorised in more than 35 markets, including the EU, the UK, and Australia.

Yahoo Finance
Oct 22nd, 2026
Galderma lifts 2026 sales growth guidance to 22.5%-23.5% after 26% Q3 jump

Swiss dermatology group Galderma raised its 2026 sales growth guidance to 22.5% to 23.5% at constant currency, up from 19% to 21%. A company-compiled analyst forecast pointed to 21.4%. Third-quarter growth was 26.0%, beating the expected 19.9%. Sales for the first nine months rose 25.1% to $4.77 billion, driven mainly by higher volumes. Galderma kept its core EBITDA margin target at about 26% as it keeps spending to support growth. Chief executive Flemming Ornskov said "robust demand for our differentiated, premium portfolio continues to drive growth." The guidance excludes the $1.5 billion all-cash purchase of ZO Skin Health, expected to close in the fourth quarter or early 2027. Galderma said the deal should slightly reduce its 2027 core EBITDA margin.

The Economic Times
Oct 21st, 2026
Beauty firms chase 'Ozempic face' market as weight-loss drugs boom.

Beauty firms chase 'Ozempic face' market as weight-loss drugs boom. By Reuters Last Updated: Oct 21, 2026, 11:32:00 AM IST Galderma, Natura, and L'Oreal are developing treatments for consumers experiencing facial sagging due to rapid weight loss. These companies are responding to increased demand linked to the popularity of GLP-1 obesity drugs. Experts indicate that rapid weight loss may lead to skin laxity and diminished facial volume. While existing treatments show promise, some limitations remain in addressing deeper facial structure issues. Swiss skincare firm Galderma, Brazilian cosmetics group Natura and beauty giant L'Oreal are testing treatments for consumers worried about facial sagging and volume loss, looking to capitalise on a growing market tied to the boom in obesity drugs. The companies are targeting concerns known as" Ozempic face ," a term that emerged as the diabetes drug became widely associated with weight loss. Experts say the loss of facial volume is linked to rapid weight loss rather than GLP-1 drugs themselves. You May Like GLP-1 drugs, such as Novo Nordisk's Ozempic and Wegovy and Eli Lilly's Zepbound, help people to lose weight by mimicking a hormone that keeps the stomach feeling full. Along with gastrointestinal side effects, the resulting rapid weight loss can also lead to loose skin on the face and body. Pfizer estimates the obesity drug market could reach $150 billion in annual sales by 2030, helping create a potentially lucrative opportunity for skincare and medical aesthetics companies as more patients seek treatments for skin laxity and facial volume loss after rapid weight loss. Revenue from these clinical treatments is projected to grow from about $700 million to $2 billion over the next five years, according to 2025 estimates by Boston Consulting Group. Michael Somenek, a Washington, DC-based facial plastic surgeon and clinical associate professor at the George Washington University School of Medicine, said he had seen a surge of requests for treatment by GLP-1 patients in the past year. "When you're looking at a large amount of weight loss over four to six months, that can really have impact on the volume within your face," he said. Companies chase the opportunity. Galderma, 20%-owned by L'Oreal, ran a study last year evaluating how some of its existing treatments perform on skin changes associated with GLP-1 weight-loss drugs. "Sagginess is a concern, loss of firmness is a concern, some hollowness can be of concern and dullness can be a concern," said Anne-Cecile Chevrier, global head of injectable aesthetics at Galderma. The Swiss company makes Sculptra, a treatment that stimulates natural collagen, and Restylane, a dermal filler made with hyaluronic acid. Chevrier said that although the treatments were not approved specifically for GLP-1 users, Galderma is working with tens of thousands of plastic surgeons and other aestheticians globally who market them to patients on weight-loss drugs. In the United States, 53% of aesthetics clinics anticipate an influx of new patients due to prescription weight-loss medications, according to a 2024 report by research firm Medical Insight, and 43% believe the increased use of these medications will drive demand for treatments addressing weight-loss-medication-induced facial changes. L'Oreal is also exploring this market. "We are now testing products on GLP-1 users in separate studies, as this group of consumers is becoming increasingly important and represents a significant number of people worldwide," said Delphine Viguier-Hovasse, L'Oreal's chief innovation and prospective officer. Manuel Krauss, Natura's chief innovation and R&D officer, said the company is testing existing products directly with GLP-1 users and developing a new generation of treatments. "GLP-1 is creating new beauty needs at unprecedented speed, but it is also showing us that the future of beauty cannot be defined by creams alone," Krauss said, noting that future innovation may combine different formats such as supplements and ingestibles. A more complicated picture. Other factors can be at play in patients experiencing skin or facial volume issues. According to analysts at the US health policy organisation KFF, GLP-1 drugs are used most widely by adults aged 50 to 64, an age group already experiencing declines in collagen and, particularly among menopausal women, estrogen production. "We don't have the research and it is probably going to be a challenging study to do because most of the female patients (on GLP-1 drugs) are perimenopausal or postmenopausal," said Heidi Young, a Northern California-based physician associate and co-owner of R+H Aesthetic Medicine. She added that some people taking GLP-1 drugs do not eat nutritious food often, which could also affect their skin: "I think it's definitely multifactorial and I don't think there is a direct answer." Do the products work? Beibei Du-Harpur, a consultant dermatologist and clinical lecturer at King's College London, said the term "Ozempic face" is misleading. "The drug doesn't melt your collagen - simply losing weight in a more sustainable, less rapid way would reduce some of the more severe changes people see." Experts said some skincare products may improve the appearance and quality of skin affected but cannot fully address the underlying loss of facial volume. "To a certain extent some of these creams can be helpful," said Dr Graeme Glass, plastic and craniofacial surgeon and aesthetic director at British beauty brand LYMA. Creams can work on the epidermis and contain molecules small enough to reach the dermis. "What they can't really do is they can't alter the ligamental structure of your face," he said. "They can't reposition the deep fat pads of the face... there is a limit to what these things can do." Du-Harpur said beauty companies were "all desperately trying to develop a GLP-1-targeting product." She said treatments such as fillers that use injections worked better than creams as they could reach the dermis, the middle and thickest layer of human skin. "What's actually losing volume is the layer below that - the fat layer - and there has never been any evidence that topical skincare products can reach that fat layer."

MarketScreener
Oct 21st, 2026
Galderma showcases data from its Injectable Aesthetics portfolio at AMWC Dubai 2026.

Galderma showcases data from its Injectable Aesthetics portfolio at AMWC Dubai 2026. Published on 10/21/2026 at 06:20 am EDT S&P Capital IQ Galderma showcased data from its Injectable Aesthetics portfolio at the Aesthetic & Anti-Aging Medicine World Congress (AMWC) taking place in Dubai, United Arab Emirates (UAE), from October 21-23, 2026. The company will present eight scientific abstracts, alongside a symposium and six Meet-the-Expert sessions, all highlighting the expanding benefits of Relfydess, Sculptra, and the Restylane range. Data on Sculptra, the first proven regenerative biostimulator, will be shared at AMWC Dubai, following its approval in the UAE expanding its current clinical application for the face to include key body areas: the gluteal area, posterior thighs and décolletage. Guidance from an international consensus panel of 11 experts will be presented, outlining evidence-based recommendations on appropriate combination strategies across approved body indications. The recommendations highlight the complementary benefits of Sculptra and Restylane SkinboostersTM in the posterior thighs, and gluteal area, for comprehensive body rejuvenation. Data from Restylane ShaypeTM? the first-and-only hyaluronic acid (HA) shaper developed with novel NASHA-HD? technology as well as expanded indications for Restylane LyftTM and Restylane VolymeTM* are being presented with clinical evidence in the chin, jawline, temples, and lower face. Across four studies, Restylane delivered well-tolerated, effective, and long-lasting aesthetic improvements in multiple facial regions, consistently achieving high responder rates and high subject satisfaction. Additionally, addressing the growing demand for body rejuvenation, data evaluating the effectiveness and safety of Restylane Skinboosters for correction of moderate-to-severe wrinkles in the décolletage will be shared at the congress, noting that the product was well tolerated and highly efficacious, with high patient satisfaction. In a dedicated symposium, international experts will discuss best practices for use of Galderma?s Injectable Aesthetics portfolio for the body through the AART? (Assessment, Anatomy, Range, and Treatment) of Body - a patient-centric technique to evaluate needs and create structured individualized treatment plans. Content will highlight the UAE expanded indications for Sculptra in the gluteal area, posterior thighs, and décolletage. Galderma will also share insights from a global survey of over 4,300 women across nine countries on menopause-related skin changes and aesthetic treatment considerations. Biostimulators and dermal fillers were the most frequently considered treatments for menopause-related facial and skin changes, with 80% of patients looking for information on Sculptra, and 75% for information on the Restylane range. Congress data also reinforces Sculptra?s ability to deliver long-term improvements in the mechanical properties of the skin, through volume restoration, improved elasticity and skin thickness. Seven experts evaluated the biostimulatory properties of Sculptra, with consensus on its key role in the regenerative aesthetic field. Data from the RELAX and EXPRESSION imaging trials confirmed early and sustained improvements in wrinkle morphology and dynamic skin strain in frown lines (glabellar lines) and crow?s feet (lateral canthal lines) following treatment with Relfydess. These findings reinforce that Relfydess delivers a rapid onset, durable efficacy, and measurable improvements in both patient-reported outcomes and skin dynamics. Pooled phase III study data for Relfydess to be presented shows improvement in moderate-to-severe frown lines and crow?s feet for both toxin-naïve and previously treated patients. Galderma will also present expert-led consensus recommendations that address key unmet needs in real-world clinical practice, offering clear, practical guidance for optimal dosing, injection patterns and treatment planning with Relfydess. Relfydess, Sculptra, and Restylane are approved in various countries around the world; approved indications vary by market. Restylane Volyme is approved as Restylane Contour in the United States. (C) S&P Capital IQ - 2026

AD HOC NEWS
Oct 20th, 2026
Galderma stock: Citi sets CHF 185.00 target for Galderma stock.

Galderma stock: Citi sets CHF 185.00 target for Galderma stock. Published on 10/20/2026 at 17:16 | Editorial responsibility: Rafael Müller, Editor-in-Chief AD HOC NEWS Revenue reached CHF 3.07 billion in the second quarter, up from CHF 2.64 billion. Galderma stock costs EUR 188.50 on October 20, 2026 at Lang & Schwarz. Analyst target and reporting date. * Citi set a CHF 185.00 target for Galderma on October 16, 2026. * Second-quarter revenue reached CHF 3.07 billion versus CHF 2.64 billion a year earlier. * Galderma stock costs EUR 188.50 at Lang & Schwarz on October 20, 2026 at 5:05 p.m. CEST. * Galderma is scheduled to release third-quarter sales and revenue on October 21, 2026. Galderma stock (ISIN CH1335392721) was trading at EUR 188.50 at Lang & Schwarz on October 20, 2026 at 5:05 p.m. CEST. On October 16, 2026, Citi analyst Cedric Besnard initiated coverage with a Buy rating and a CHF 185.00 price target, according to Markets Insider. The target is 5.47 percent above the SIX price of CHF 175.40 at 4:54 p.m. CEST. Discover more Hire M&A Advisors Open Bank Account Read Company News Revenue growth supports the case. Galderma reported CHF 3.07 billion in quarterly revenue for the period ending June 30, 2026, compared with CHF 2.64 billion a year earlier. That represents growth of 16.29 percent. The figures were carried by Markets Insider in its report on the Citi initiation. Stock sits near its yearly high. Galderma traded between CHF 96.50 and CHF 188.25 over the 52 weeks through October 20, 2026. Its SIX market capitalization was CHF 40.9 billion, with a price-to-earnings ratio of 58.41. The CHF 175.40 share price stood 6.83 percent below the 52-week high, leaving the valuation sensitive to the company meeting its growth plans. Next report arrives October 21. Galderma is scheduled to release third-quarter sales and revenue on October 21, 2026, according to MarketScreener. The date gives investors the next test for revenue momentum and margin delivery. Galderma also remains a member of the Swiss Market Index, as Galderma reported on September 21, 2026. Comparison with peers. Galderma: 0.98 percent higher on SIX, P/E 58.41, market capitalization CHF 40.9 billion. Novartis: 1.61 percent higher on SIX, P/E 23.32, market capitalization CHF 239.9 billion. AbbVie: 2.02 percent higher on NYSE, P/E 81.34, market capitalization USD 509.6 billion. Target and price in view. Discover more Check Loan Rates Track Biotech Read Economics Citi's CHF 185.00 target is 5.47 percent above the SIX price of CHF 175.40, while the Lang & Schwarz euro quote provides the German trading perspective for the stock. The next scheduled report is the immediate event date for assessing whether revenue growth remains consistent with the analyst case. Galderma was trading at EUR 188.50 at Lang & Schwarz on October 20, 2026 at 5:05 p.m. CEST. The further course of trading is shown by the continuously updated real-time quote of Galderma stock. Galderma market data. * Company: Galderma Group AG * ISIN: CH1335392721 * Ticker: GALD * Primary exchange: SIX * Price Lang & Schwarz (as of October 20, 2026, 5:05 p.m. CEST): EUR 188.50 * Market capitalization: CHF 40.9 billion (as of October 20, 2026) * 52-week range: CHF 96.50-188.25 (as of October 20, 2026) * Sector / Industry: Personal Products * Index membership: SMI * Next earnings date: October 21, 2026 Sponsored Ad Galderma stock: new analysis - 22 October. Discover more Invest in Stocks Fresh Galderma information released. What's the impact for investors? Our latest independent report examines recent figures and market trends. Disclaimer regarding our articles: This is not investment advice, nor is it a recommendation to buy or sell. Information regarding prices, companies, and markets is provided without guarantee; changes may occur at any time. Stock market transactions can result in significant losses. Our articles are created and reviewed, in whole or in part, automatically with the assistance of AI. en | CH1335392721 | GALDERMA | boerse | 70375525 | bgmi