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Über
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My client are a global contract developer and manufacturer supporting the medical‑device industry with end‑to‑end capabilities across research, engineering, and large‑scale production.
About
My client are a global contract developer and manufacturer supporting the medical‑device industry with end‑to‑end capabilities across research, engineering, and large‑scale production.
Duties / Responsibilities
- Manage a portfolio of 3–5 strategic Key Accounts, prioritising top‑tier OEMs while also cultivating relationships with other high‑potential market players.
- Achieve annual sales growth and revenue targets as defined in the business plan.
- Accurately forecast quarterly and annual revenue based on a defined sales pipeline, maintaining forecast accuracy within ±15%.
- Lead and successfully pass a minimum of 2–3 major supplier qualification audits with key customers per year.
- Drive the technical sales process to secure “design‑in” status in at least 1–2 major new customer programs annually.
- Strategic Account Leadership: Develop and execute long‑term, multi‑year account strategies that transition relationships from transactional suppliers to valued technical partners. Deeply understand the customer’s business, R&D roadmap, and competitive landscape.
- Technical Solution Selling: Act as a critical bridge between customer engineering teams and internal R&D. Must articulate complex technical value propositions and translate customer needs into actionable product/process specifications.
- Cross‑Functional Collaboration & Influence: Lead without direct authority through coordinating with internal R&D, Quality, Operations, and Supply Chain to resolve critical issues, ensure on‑time delivery, and align resources to meet strategic account objectives.
- Compliance & Quality Stewardship: Serve as a frontline guardian of the company’s quality and regulatory standards. Ensure all proposals, communications, and agreements comply with relevant regulations (e.g., FDA QSR, ISO 13485).
- Industry Insight & Consultative Approach: Maintain a deep understanding of downstream medical device trends. Proactively advise customers on new materials, technologies, or processes to improve product performance or time‑to‑market, positioning the company as a thought leader.
Qualification
- Biomedical engineering, polymer materials, mechanical automation, biology, or related STEM fields, with the ability to interpret technical drawings and standards (e.g., ISO, ASTM).
- Deep Product & Regulatory Knowledge: Must be proficient in the underlying material science, manufacturing processes, biocompatibility, sterilisation adaptability, and regulatory requirements (e.g., FDA 21 CFR Part 820, ISO 13485) of the products.
- Complex Sales Competency: Demonstrated ability to engage in professional dialogue with multiple client-side departments such as R&D, Purchasing, Quality, and Production.
Experience Required
Proven Key Account & Project Management experience: Direct experience managing complex, long‑cycle sales projects (from design‑in to validation) with major medical device OEMs.
Technical Bridge & Compliance Foundation: Strong ability to translate technical product/process details and lead rigorous supplier qualification audits, ensuring adherence to quality (e.g., ISO 13485) and regulatory standards. xcfaprz
Strategic Customer Integration: Demonstrated success engaging with client R&D teams early in their design phase to become a strategic “design‑in” partner and provide valued technical input.
For further information, contact Alan on alan(at)accpro(dot)ie
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Sprachkenntnisse
- English
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