Global PV Risk Minimization Physician Injectable Aesthetics

Q-Med Aktiebolag; Uppsala kommun; Vor Ort; SEK 1.000.000 - 1.750.000; Vollzeit

Zusammenfassung

Galderma in Uppsala, Sweden seeks a Global PV Risk Minimization Physician for its Injectable Aesthetics portfolio. You will provide medical leadership across pharmacovigilance, risk management, and post-marketing safety, collaborating with Regulatory Affairs, Clinical Development, Medical Affairs, and Quality to shape safety strategies on a global scale.

This is a pivotal role requiring deep medical expertise, cross-functional influence, and a commitment to patient safety in a rapidly evolving

Qualifikationen

• Extensive experience in medical device safety and pharmacovigilance.
• Proven ability to lead cross-functional teams across global functions.
• Strong knowledge of risk management and benefit-risk assessments.

Aufgaben

• Lead medical evaluations of safety data and signals.
• Develop and drive global risk minimisation strategies.
• Contribute to regulatory submissions and safety reports.
• Collaborate with Health Authorities and cross-functional teams worldwide.

Kenntnisse

Global PV safety

Regulatory liaison

Cross-functional leadership

Ausbildung

MD / Doctor of Medicine

Tools

Safety databases

Regulatory guidelines

Jobbeschreibung

Global PV Risk Minimization Physician Injectable Aesthetics

Kommun: Uppsala

We are looking for a Global PV Risk Minimization Physician to join our Global Pharmacovigilance organisation within Injectable Aesthetics.

This is an influential global role for a physician with deep expertise in medical device vigilance, risk management, and post-marketing safety. You will provide medical and scientific leadership across Galderma's portfolio of injectable aesthetic medical devices, helping ensure that patient safety and benefit-risk considerations remain at the centre of product lifecycle management and strategic decision-making.

Working in a highly collaborative international environment, you will partner with colleagues across Pharmacovigilance, Clinical Development, Medical Affairs, Regulatory Affairs, Quality, and Commercial teams. Together, you will shape safety strategies, guide regulatory interactions, and contribute to decisions that impact healthcare professionals and patients worldwide.

This is a unique opportunity to combine scientific expertise, strategic thinking, and cross-functional leadership in one of the most innovative and rapidly evolving areas of dermatology.

Your mission

As Global PV Risk Minimization Physician, you will provide medical leadership for post-marketing safety and risk management activities across Galderma's Injectable Aesthetics medical device portfolio.

You will play a key role in shaping global safety strategies, leading benefit-risk evaluations, and driving initiatives that support the safe use of our products throughout their lifecycle. Working in close partnership with colleagues across Pharmacovigilance, Clinical Development, Medical Affairs, Regulatory Affairs, Quality, and Commercial teams, you will contribute scientific expertise that informs critical business and regulatory decisions.

In this role, you will:

Lead medical assessments of safety data, emerging signals, and benefit-risk profiles.

Drive risk minimisation strategies and support their implementation globally.

Provide expert input into regulatory submissions, safety reports, and product labelling.

Support interactions with Health Authorities, Competent Authorities, and Notified Bodies.

Contribute to safety governance and cross-functional decision-making.

Strengthen inspection readiness and support a culture of compliance, patient safety, and continuous improvement.

Act as a trusted scientific partner across the organisation and help shape the future of Injectable Aesthetics at Galderma.

Your profile

You are a physician with a passion for patient safety and a strong scientific mindset. Drawing on extensive experience in medical device safety, vigilance, risk management, or related post-marketing activities, you combine deep medical expertise with the ability to navigate complex global environments and build strong partnerships across functions, cultures, and geographies.

You are comfortable translating complex scientific data into clear recommendations and practical actions, influencing stakeholders at different levels, and balancing strategic thinking with operational execution. With strong scientific judgement, a collaborative approach, and high ethical standards, you thrive in a dynamic international environment where patient safety, quality, and compliance are at the centre of decision-making.

What you'll bring:

• 10-15 years of relevantexperience within global medical device safety, vigilance, risk management, or related post-marketing activities.
• Strong knowledge of benefit-risk assessment, signal detection, safety surveillance, and risk minimization.
• Solid understanding of global medical device regulations and vigilance requirements.
• Experience interacting with Health Authorities, Competent Authorities, and/or Notified Bodies.
• Knowledge of epidemiology, statistics, and safety data evaluation.
• Strong analytical skills and the ability to interpret complex safety data and translate insights into action.
• Proven ability to lead initiatives and influence stakeholders within a global matrix organization.
• Excellent communication and collaboration skills, with the ability to engage effectively across functions and cultures.
• A proactive, adaptable, and solutions-oriented mindset.
• Fluency in written and spoken English.

Additional qualifications in Clinical Pharmacology, Drug Safety, Public Health, Epidemiology, Biomedical Engineering, or related disciplines are considered an advantage.

Location and information

This position is based on-site in Uppsala, Sweden.

Why Galderma

At Galderma, you'll have the opportunity to work in a science-driven, innovative, and collaborative environment where quality and patient impact are at the center of everything we do. You'll join a team of talented colleagues and play an important role in supporting the continued growth of our biologics and protein-based portfolio.

Krav

• Specialistläkare, klinisk farmakologi - 5 års erfarenhet eller mer