Cochlear

Borken, DE
Total Offices: 3
4,464 Total Employees
Year Founded: 1981

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Jobs at Cochlear

Search the 29 jobs at Cochlear

Recently posted jobs

3 Days Ago
Macquarie Island, Tasmania, AUS
Healthtech • Pharmaceutical • Manufacturing
Cochlear is seeking a Procurement Manager to lead procurement activities from new product development to ongoing supply of goods and services, ensuring maximum value and achievement of key performance indicators. This role involves managing procurement team members, overseeing supplier performance, and influencing stakeholders to comply with procurement policies.
Healthtech • Pharmaceutical • Manufacturing
Lead a team of reimbursement specialists in processing insurance orders, provide coaching and mentoring, ensure high customer service standards, and drive team performance to exceed reimbursement goals.
5 Days Ago
Macquarie Island, Tasmania, AUS
Healthtech • Pharmaceutical • Manufacturing
Lead end-to-end project management for embedded software and firmware development, collaborate with cross-functional teams, define project scope and objectives, develop project plans, manage resources, identify and mitigate risks, liaise with stakeholders.
6 Days Ago
Vallauris, Alpes-Maritimes, Provence-Alpes-Côte d'Azur, FRA
Healthtech • Pharmaceutical • Manufacturing
As a Technicien.ne Expert in product investigation at Cochlear, you will conduct investigations on the causes of implant failures, prepare failure analysis reports, ensure traceability of operations, and propose process improvements for productivity and quality. Minimum qualification of Bac + 2 in technical field required.
6 Days Ago
Melbourne, Victoria, AUS
Healthtech • Pharmaceutical • Manufacturing
Seeking a Sales Professional to join the newly formed team at Cochlear and contribute to business growth by providing industry-leading surgical and clinical support. Responsibilities include supporting sales targets, customer training, and clinical support for surgical/hearing centers. Opportunity for career development and working on innovative projects at Cochlear.
6 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
The Customer Software Verification and Validation Engineer at Cochlear is responsible for ensuring high-quality and on-time delivery of complex projects related to customer software products. This role involves defining, executing, and reporting tests, collaborating with stakeholders, and maintaining regulatory compliance.
6 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
The Senior Hardware Verification Engineer - Technical Lead will lead a team in planning, organizing, and executing verification tasks for implantable hearing devices. They will ensure compliance with international standards, champion improvements in verification processes, and collaborate with global teams.
6 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
The Hardware Verification Engineer will be responsible for planning, organizing, and executing verification tasks to support product development, ensuring compliance with international standards. They will collaborate with global and local teams, develop test methods, and perform engineering tasks to sustain approved products on the market.
8 Days Ago
Osaka, JPN
Healthtech • Pharmaceutical • Manufacturing
Cochlear, a global leader in implant hearing solutions, is seeking a Sales Executive based in Osaka to expand the business in Kansai. Responsibilities include achieving sales targets, providing information about products and services, planning strategies for surgery increase, building relationships with professionals, and increasing awareness about cochlear implants.
Healthtech • Pharmaceutical • Manufacturing
The Senior Specialist, Marketing Communications at Cochlear will drive the business strategy for Japan, ensuring customer engagement and satisfaction while maximizing revenue opportunities. Responsibilities include developing and executing marketing communications plans, analyzing market data, creating marketing collaterals, and organizing events and promotions.
8 Days Ago
Lone Tree, CO, USA
Healthtech • Pharmaceutical • Manufacturing
The Senior Quality Specialist at Cochlear is responsible for managing the Quality Management System, conducting internal audits, and ensuring compliance with medical device regulations. Key responsibilities include facilitating root cause analysis, leading improvement projects, and delivering quality training programs. The role requires 3+ years of quality experience in a regulated industry with knowledge of ISO 13485 and continuous improvement methodologies.
8 Days Ago
Mechelen, BEL
Healthtech • Pharmaceutical • Manufacturing
As a Software Product Owner at Cochlear, you will shape the product vision and roadmap, prioritize backlog items, define requirements for the development team, and lead collaborations across different teams to ensure product success and alignment with organizational goals. You will also be a subject matter expert, guiding interactions with various functions and teams.
8 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
Responsible for obtaining Customs Rulings, introducing Licenced Manufacturing Warehouse, supporting logistics operations, implementing lean practices, collaborating with departments, ensuring compliance, and optimizing transportation processes. Support project teams and continuous improvement efforts in logistics.
8 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
Responsible for controlling all movements from receiving of raw materials to dispatching of finished products in a manufacturing environment. Key responsibilities include receiving shipments, handling materials, packing items for shipping, and participating in quality and safety practices. Requires a minimum diploma in Logistics and 1-3 years of experience in warehouse/logistics operations.
8 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
The Device Analysis Engineer at Cochlear is responsible for performing testing on Cochlear devices, identifying failure modes, and coordinating device analysis data to management. The role requires a Bachelor's degree in engineering, 3 years of relevant experience, Python skills, and strong analytical abilities.
8 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
Oversee the successful delivery of test systems, ensuring quality standards and alignment with objectives. Develop project plans, foster a collaborative work environment, communicate with stakeholders, implement QA processes, and manage resources effectively.
8 Days Ago
Brisbane, Queensland, AUS
Healthtech • Pharmaceutical • Manufacturing
Develop and implement manufacturing processes, manage complex projects, ensure high-quality products, lead team development, drive manufacturing technology introduction.
8 Days Ago
Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, MYS
Healthtech • Pharmaceutical • Manufacturing
The Complaints Specialist at Cochlear Malaysia is responsible for receiving, evaluating, and reporting complaints related to medical devices. This role involves gathering complaint details, monitoring and progressing complaints, maintaining accurate records, providing support and training, and identifying process improvements.
Healthtech • Pharmaceutical • Manufacturing
The Platform ASIC Project Manager will manage and coordinate the development of one or more Platform and/or ASIC projects within the hardware platform group. Responsibilities include project management, risk management, stakeholder engagement, and contributing to future platform definition for Cochlear products.
Healthtech • Pharmaceutical • Manufacturing
Lead and grow technical expertise in design control activities for medical devices. Provide expert guidance in sustaining products and developing new ones. Ensure compliance with regulatory requirements and maintain high-quality technical documentation throughout the product lifecycle.