Technical Advisor - Biocompatibility/Chemistry
Listed on 2026-10-03
-
Engineering
Technical Advisor
- Biocompatibility/Chemistry
Job Description Job Alerts Link Technical Advisor
- Biocompatibility/Chemistry
At TÜV SÜD Group we are passionate about technology. Innovations impact our daily lives in countless ways, and we are dedicated to being a part of that progress. We test, we audit, we inspect, we advise. We never stop challenging ourselves for the safety of society and its people. We breathe technology, we strive for professional excellence, and we leave a mark.
We take the future into our hands. We are TÜV SÜD Group.
- Biocompatibility & Chemistry Your Tasks
As a Technical Advisor, Medical Device Testing
- Biocompatibility & Chemistry, you will serve as a trusted technical partner to our Account Executives, helping customers identify the right testing and compliance solutions for their medical devices. You will bridge customer requirements with TÜV SÜD's technical capabilities, supporting business growth through technical expertise, solution development, and customer engagement.
- Partner with Account Executives throughout the sales process to understand customer needs and develop technically sound testing solutions.
- Develop project scopes, testing strategies, project plans, and cost estimates for biocompatibility and chemistry testing programs.
- Translate customer requirements into comprehensive proposals aligned with TÜV SÜD quality and technical standards.
- Research and evaluate solutions for customer needs that extend beyond current service offerings.
- Collaborate with laboratory leaders, technical experts, consultants, and external partners to identify and develop new testing capabilities.
- Participate in customer meetings, technical discussions, proposal reviews, and sales presentations to support business development activities.
- Provide guidance on medical device regulatory requirements and testing expectations, including FDA, EU MDR, Health Canada, and other applicable frameworks.
- Serve as the technical point of contact during the pre‑sales process and facilitate a smooth transition to project delivery teams following contract award.
- Monitor industry trends, emerging technologies, and regulatory developments to identify opportunities for service expansion and innovation.
Required Qualifications
- Bachelor's degree in Engineering, Life Sciences, Chemistry, Biology, Biomedical Engineering, or a related technical discipline.
- Minimum of 3 years of experience in a technical, applications engineering, solutions engineering, pre‑sales, regulatory, or testing role within the medical device industry.
- Strong understanding of medical device testing, regulatory requirements, and compliance pathways.
- Experience developing technical scopes of work, project plans, and customer proposals.
- Knowledge of biocompatibility and chemistry testing applicable to medical devices.
- Excellent communication and presentation skills with the ability to explain complex technical information to diverse audiences.
- Strong analytical and problem‑solving abilities.
- Ability to work independently while collaborating effectively across technical, commercial, and operational teams.
- Advanced degree in Engineering, Life Sciences, Toxicology, Chemistry, Biomedical Engineering, or a related field.
- Experience supporting ISO 10993 biological evaluation programs.
- Experience with in a testing, inspection, certification, consulting, or regulatory services organization.
- Familiarity with FDA, EU MDR, Health Canada, and other global medical device regulatory frameworks.
- Experience working directly with medical device manufacturers.
- Experience researching and developing new service offerings or technical solutions.
- Opportunity to work with a…
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