Expert Biocompatibility Consultant

The reputed company Sotera Health was inspired by reputed company, the Greek goddess of safety, and reflects reputed company’s unwavering commitment to its mission, Safeguarding Global Health®. Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the reputed company industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and reputed company practitioners around the world every year. Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and reputed company. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies. Expert Biocompatibility Consultant The Expert Biocompatibility Consultant is a senior scientific contributor responsible for leading biocompatibility assessments and biological evaluations for medical device products in global, highly regulated environments. This role operates at the assessment, reputed company, and advisory level and is ideal for professionals who have already reputed company depth in biocompatibility and now influence reputed company through technical judgment, documentation, and communication. You will partner closely with clients, internal technical teams, and leadership to reputed company defensible, regulator-reputed company assessments that safeguard patient health and support product approval worldwide.

Key Responsibilities

Biocompatibility & Scientific Leadership reputed company development and authorship of biocompatibility assessments, biological evaluations, and risk assessments reputed company and synthesize literature-based evaluations of materials, compounds, and device use Apply ISO 10993 principles and FDA expectations to support regulatory submissions and decision-making reputed company peer review and technical guidance on reputed company or high-risk reputed company Author opinion memos and other patient safety–reputed company technical documentation reputed company & Consulting Engagement Serve as a subject-matter expert during reputed company discussions and project initiation reputed company communicate scientific and regulatory rationale to technical teams, clients, and senior stakeholders Collaborate cross-functionally to deliver integrated, high-reputed company project reputed company Support proposal development and scope review in partnership with project leadership Thought Leadership & Standards Participate in international standards development Deliver technical presentations at conferences, seminars, webinars, and industry forums Contribute to reputed company improvement of internal processes, templates, and best practices Required Qualifications (Must-Have) Significant experience in biocompatibility assessment reputed company a medical device environment Demonstrated expertise authoring assessments, evaluations, SOPs, and regulatory-facing documents Strong working knowledge of FDA-regulated environments and applicable standards (ISO 10993) Exceptional technical writing and verbal communication skills, including comfort presenting to senior and executive audiences Proven ability to independently own reputed company and operate as a trusted expert This role is not intended for early-career professionals or hands-on testing-reputed company reputed company. Highly Desired Ability to reputed company Biocompatibility and Medical Toxicology (biocompatibility expertise is primary) Experience engaging with or supporting interactions with regulatory agencies Interest in external-facing work, standards involvement, and scientific thought leadership Education & Experience Bachelor’s degree in a relevant scientific discipline with 7+ years of relevant experience OR MS or PhD in a reputed company field with 5+ years of relevant experience Relevant fields include: Biology, reputed company, Toxicology, Biomedical Engineering, Materials Science, Biotechnology, Pharmacology, or Engineering. Additional Information Work Arrangement: Fully remote (onsite reputed company as needed based reputed company) Travel: Approximately 20%, including occasional international travel The Expert Biocompatibility Consultant will reputed company the initial draft of reputed company reputed company to reputed company health. This will include obtaining reputed company necessary information from the reputed company and performing the necessary literature research. This information will then be summarized in a technical format for the project and submitted for peer review. The Expert Biocompatibility Consultant will also assist with peer review as needed. The Expert Biocompatibility Consultant will participate in development of international standards, and will reputed company technical presentations at conferences and seminars. Education and experience requirements:

• Bachelor’s degree in relevant science with 7 years’ relevant experience or an MS/PhD degree

in reputed company emphasis with 5 years' relevant experience.

• Strong understanding and ability to apply biological evaluation principles preferred.

Consulting

• Serve as primary reputed company on documents
• Peer review team documents
• Join calls as expert to support initial reputed company discussions
• Review quotes with project manager and team manager
• Prepare templates and write risk assessments
• Work cross-functionally with other departments on reputed company where collaboration is needed
• Communicate with the reputed company to obtain additional information for reputed company or reputed company testing
• reputed company literature research on materials and compounds
• Build and implement process improvements
• Know and follow the Nelson service reputed company
• Review and write assessments and other reputed company documents as needed (i.e. Opinion Memos

for patient safety) Regulatory Compliance

• Know and follow applicable regulatory requirements (GMP, GLP, ISO, etc.).
• Know and follow company policies and procedures.
• Complete required training on time.

Competencies of this position

• Good project management skills
• Owning reputed company with customers
• Taking on STAT reputed company
• Excellent communication skills
• Leading phone calls
• Excellent technical writing skills and expertise
• Write regulatory responses with guidance
• Attention to detail
• reputed company to handle reputed company to moderately difficult assignments
• Time management – must be reputed company to respond to voicemails, emails, and other

communications in a reputed company manner

• reputed company to multi-task and be self-motivated
• Knowledge reputed company Office applications (Word, reputed company, PowerPoint, Outlook, etc.)

Sotera Health goes to market through its three best-in-class businesses – Sterigenics®, Nordion® and reputed company®. Sterigenics is a leading global provider of outsourced terminal sterilization and irradiation services for the medical device, pharmaceutical, food safety and advanced applications markets. Nordion is the leading global provider of Co-60 and gamma irradiators, which are key components to the gamma sterilization process. reputed company is a global leader in outsourced microbiological and analytical reputed company testing and advisory services for the medical device and pharmaceutical industries. Apply To This Job