Global Medical Affairs Senior Manager

Silimed® Implants; España; On-site; PHP 8,708,000 - 13,062,000; Full time

Benefits offered by this job

Full remote position

Job summary

Silimed, a global silicone implant manufacturer, is seeking an experienced Medical Affairs leader to steer global scientific initiatives, partnerships with KOLs, and evidence-generation programs across regions. You will provide medical leadership throughout the product lifecycle, review claims, and ensure regulatory alignment while collaborating with Regulatory, Quality, Marketing, and Clinical teams.

The role offers a fully remote arrangement within Europe, with collaboration across

Qualifications

• Bachelor’s degree in Life Sciences or related healthcare field.
• PhD or Master’s in healthcare is mandatory if no breast implant experience.

Responsibilities

• Support development of global Medical Affairs strategies and scientific initiatives.
• Establish and maintain scientific partnerships with KOLs and investigators.
• Lead scientific exchange with external experts and communicate clinical data.
• Identify evidence gaps and support IIS, RWE, and publications.
• Provide medical leadership across the product lifecycle and lifecycle management.
• Review scientific and promotional claims for accuracy and regulatory compliance.
• Collaborate with Regulatory, Quality, Marketing and Commercial teams.

Skills

Scientific acumen

Medical storytelling

KOL engagement

Cross-functional collaboration

Project management

Regulatory compliance

Evidence generation

Education

Bachelor's in Life Sciences / related healthcare

PhD or Master's in healthcare

Job description

About Us

Founded in Brazil in 1978, Silimed is a global manufacturer of silicone implants for aesthetic and reconstructive surgery. With more than four decades of experience, the company has developed one of the most comprehensive portfolios in the category, offering multiple surface technologies, shape formats, and projection options designed to support individualized surgical planning.

Working in close collaboration with plastic surgeons, Silimed® integrates clinical insight into product development, aligning design with real-world surgical needs. Its implants are manufactured under rigorous quality standards and comply with internationally recognized regulations, including European CE certification.

Rooted in Brazilian-origin innovation, Silimed® combines technical expertise with a structured and versatile design system, supporting a wide range of surgical approaches across global markets.

Silimed's vocation is to contribute to plastic surgery, promoting both research and scientific studies, and developing technologies to meet different needs. Silimed was the first company in the world to identify each implant with an individual serial number, allowing product traceability and providing more safety to doctors and patients.

Key Responsibilities

• Support the development and execution of global Medical Affairs strategies and scientific initiatives, ensuring alignment with corporate objectives and regional needs.
• Develop and maintain strategic scientific partnerships with Key Opinion Leaders (KOLs), investigators, and other healthcare stakeholders to foster scientific collaboration and generate actionable medical insights.
• Lead scientific exchange with external experts, ensuring balanced, evidence-based communication of clinical data and product information.
• Identify evidence gaps and support evidence generation initiatives, including investigator-initiated studies (IIS), real-world evidence (RWE), clinical publications, and scientific collaborations.
• Gather, analyze, and communicate medical insights from healthcare professionals, KOLs, and international markets to inform medical strategy, product lifecycle management, and future evidence-generation activities.
• Provide scientific leadership and medical support throughout the product lifecycle, including clinical evidence dissemination, scientific communications, and responses to medical information requests.
• Review and approve scientific and promotional claims, marketing materials, educational content, and external communications to ensure scientific accuracy, clinical relevance, regulatory compliance, and consistency with approved product labeling.
• Partner closely with Clinical Affairs, Regulatory Affairs, Quality, Marketing, Market Access, and Commercial teams to ensure cross-functional alignment while maintaining Medical Affairs independence and scientific integrity.
• Contribute to the planning and execution of advisory boards, scientific congresses, expert meetings, and publication strategies to strengthen external scientific engagement.
• Support the development, review, and approval of scientific publications, abstracts, manuscripts, medical presentations, and evidence summaries.
• Monitor emerging scientific literature, clinical evidence, treatment guidelines, competitor activities, and healthcare trends to identify opportunities and support strategic medical planning.
• Ensure all Medical Affairs activities are conducted in accordance with applicable regulations, ethical standards, industry codes of practice, and company compliance policies.

Your profile

Education

• Bachelor's degree in Life Sciences, Pharmacy, Medicine, Biomedical Sciences, or a related healthcare discipline.
• PhD or master’s in healthcare is considered mandatory if there is no previous experience in breast implants.

Experience

• Minimum 10 years of experience within the pharmaceutical, biotechnology, or medical device industry. Experience in breast implants will be considered a plus
• Previous exposure to Medical Affairs, Medical Education, scientific projects, or healthcare stakeholder engagement is preferred.

Languages

• Fluent English is required.
• Fluent Spanish and basic Portuguese are highly desirable and would be considered an asset

Key Competencies

• Strong scientific acumen with the ability to critically evaluate, interpret, and communicate clinical evidence.
• Excellence in scientific communication and medical storytelling for both internal and external stakeholders.
• Proven ability to develop and maintain trusted scientific partnerships with Key Opinion Leaders (KOLs), investigators, and healthcare professionals.
• Expertise in KOL engagement, medical insight generation, and translating field insights into actionable medical strategies.
• Strong understanding of Medical Affairs principles, scientific exchange, evidence generation, and product lifecycle management.
• Experience reviewing scientific claims and promotional materials to ensure scientific accuracy, regulatory compliance, and alignment with approved labeling.
• Strategic thinking with the ability to identify evidence gaps, emerging clinical trends, and opportunities to strengthen the scientific value proposition.
• Excellent cross-functional collaboration skills, with the ability to influence without authority while maintaining Medical Affairs independence.
• Strong project management and organizational skills, with the ability to prioritize multiple initiatives in a fast-paced global environment.
• High ethical standards, sound scientific judgment, and commitment to compliance with industry regulations and codes of practice.
• Adaptability and effectiveness in working within multicultural, cross-regional, and matrix organizations.

Why us?

• Full remote position wihtin one of our HQ in Europe. (Austria, Belgium, Germany, Denmark, Netherlands, Spain, Italy, Turkey, UK)