13 часов назад
Assoc/Assoc I - Product Surveillance
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Assoc/Assoc I - Product Surveillance (Medical Devices): Managing medical product complaints and MDRs, including reportability assessment, regulatory reporting, investigations, and customer follow-up with an accent on product surveillance, complaint workflow, and regulatory compliance. Focus on triaging communications, coordinating sample retrieval, escalating issues, and closing complaint records accurately and on time.
Location: Gurgaon, Haryana, India
Company
develops healthcare products and solutions focused on improving healthcare delivery and saving and sustaining lives.
What you will do
- Manage and process product complaints and Medical Device Reports across multiple product lines.
- Open complaint records, collect required information, and conduct written and verbal customer follow-up.
- Assess complaint reportability and prepare regulatory reports in accordance with applicable regulations.
- Evaluate investigation requirements, coordinate sample retrieval, respond to customers, and close complaints according to procedure.
- Manage workflow, triage internal and external communications, and escalate issues when needed.
- Participate in continuous improvement projects and support or mentor less experienced team members.
Requirements
- Fluent English with strong written and verbal communication skills.
- Associate’s degree in nursing, pharmacy, medical technology, engineering, or a scientific field, or equivalent experience.
- Two to three years of experience in a cGMP-related industry or clinical setting.
- Ability to prioritize, multitask, work independently, and collaborate with cross-functional teams.
- Strong critical-thinking, problem-solving, computer, detail-orientation, and customer-service skills.
Nice to have
- Bachelor’s degree or clinical certification such as MT or RN.
- Project management experience or certification.
- Experience overseeing complaint-handling and reporting activities or mentoring new team members.
Culture & Benefits
- Full-time employment in a healthcare-focused organization.
- Culture centered on courage, trust, collaboration, ownership, and accountability.
- Opportunities to contribute to continuous improvement and cross-functional projects.
- Reasonable accommodations are available for candidates with disabilities during the application and interview process.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
2 часа назад
Manager, Regulatory Affairs (Medtech)
7 дней назад
Complaint Handling Specialist (Medical Devices)
66 000 - 75 000$
15 часов назад
International Regulatory Specialist (Medical Devices)
6 дней назад
Medical Affairs Manager (Medical Devices)
24 часа назад
Associate Director GRA CMC SaMD & Cybersecurity Specialist
3 дня назад
Sr Regulatory Affairs Specialist (Medical Devices)
85 000 - 130 000$