6 дней назад
Senior Business Development Executive (Medical Devices)
5 000 - 6 000MYR
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Business Development Executive (Medical Devices): Driving customer acquisition and account growth for medical device regulatory, certification, and compliance services with an accent on ISO 13485, MDSAP, EU MDR, FDA, and ASEAN requirements. Focus on translating technical regulations into commercial solutions, developing sales opportunities, negotiating contracts, and closing deals.
Location: Shah Alam, Selangor, Malaysia
Salary: MYR 5,000–6,000 per month
Company
provides testing, inspection, certification, sustainability, quality, and integrity services through a global network of offices and laboratories.
What you will do
- Drive new customer acquisition, account expansion, revenue growth, and market penetration for medical device management and compliance services.
- Identify, develop, and manage opportunities involving certification, regulatory compliance, supplier audits, technical documentation review, and lifecycle compliance.
- Promote services related to ISO 13485, MDSAP, EU MDR, FDA, and ASEAN medical device regulations.
- Prepare client presentations, proposals, and commercial offers with technical and operations teams.
- Build and maintain client relationships through meetings, follow-ups, account reviews, negotiations, and contract closure.
- Track sales activity in CRM tools, report pipeline and performance, monitor market developments, and provide feedback to marketing and product development teams.
Requirements
- Bachelor’s degree in Engineering, Biomedical, Life Sciences, Quality, Regulatory Affairs, or a related discipline.
- 3–5 years of experience in business development, sales, or commercial roles within medical devices, regulatory, certification, or compliance services.
- Experience working with medical device manufacturers, distributors, or importers.
- Strong understanding of medical device regulations and quality management systems, including ISO 13485, MDSAP, EU MDR, FDA 21 CFR, and/or ASEAN regulations.
- Proven sales, negotiation, closing, presentation, stakeholder management, and relationship-building skills.
- Ability to work independently and collaborate effectively with cross-functional and multicultural teams.
Culture & Benefits
- Full-time employment in an international testing, inspection, and certification organization.
- Work with operations, technical, marketing, and product development teams.
- Responsibilities require adherence to integrity, professional conduct, health, safety, and environment policies.
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