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AccuPath® employs over 1,000 people in all countries. We are constantly searching for motivated, enthusiastic and talented individuals to help us continue to deliver on our mission. If you are excited about providing solutions that keep businesses in motion, check our open job opportunities and apply.

Job requirements

Job requirements

Role Description:

● Develop the technical department's work plan, technical roadmap, product planning, talent planning, and project plans based on the company and division's development strategies.
● Manage technical department operations, including product development projects, NPI projects, improvement project management, major decision-making, and achieving department management targets.
● Lead technology introduction and innovation, participate in and supervise project initiation, R&D, and implementation of products. Develop intellectual property strategies, intellectual property protection, technology transfer, and talent recruitment and development.
● Ensure operational technical support and process assurance, including monitoring the quality, cost, and efficiency of products after transfer to production. Lead the advancement of manufacturing equipment and processes.
● Team building, personnel evaluation, morale enhancement, and other tasks assigned by the Division General Manager.

Main Challenges:

● Drive continuous process R&D and overcome limitations of existing manufacturing methods for balloon catheters, ensuring absolute competitiveness in quality, cost, and efficiency.
● Drive continuous development of balloon catheter products across all areas, creating a comprehensive, high-performance, and multifunctional product matrix.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher in Polymer Materials or a related field.
● 5+ years of product R&D or process experience in balloon catheter interventions, 8+ years of experience in implantation/interventional products, and 5+ years of technical team management experience with a team size of at least 5 people.

Personal Attributes:

● Ability to understand industry competitors' product strengths and weaknesses, future product technology trends, product planning and development, project management experience, and supply chain management experience.
● Excellent communication, collaboration, and learning abilities, with talent pipeline management skills and strong self-drive. Entrepreneurial spirit is a plus.

Job requirements

Job requirements

Role Description:

● Market Analysis: Collect and provide feedback on market information based on company market strategy, local market characteristics, and industry trends.
● Market Expansion: Develop sales plans, explore potential markets, identify customer needs, and provide solutions. Optimize sales strategies based on market research and analysis to achieve sales targets.
● Customer Management: Consolidate customer information, develop customer follow-up plans, and maintain customer relationships. Implement business contracts, confidentiality agreements, technical standards, and framework service agreements. Coordinate order delivery, payment progress, and confirmation of export documentation. Follow up on post-sales issues.
● Marketing Activities: Plan and participate in various marketing activities, such as medical exhibitions, industry conferences, and product launches.

Main Challenges:

● Conducting market research and analysis for overseas markets, identifying potential market opportunities, and expanding into new markets.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher, preferably in materials-related disciplines.
● 5+ years of business development experience in the medical device or medical applications of polymer materials field.

Personal Attributes:

● Fluent in English and familiar with the local medical device market environment.
● Strong independent customer development, negotiation, communication, and coordination skills. Proactive, team-oriented, adaptable, and willing to travel.

Job requirements

Job requirements

Role Description:

● Actively visit existing clients, identify new projects, explore customer potential, and achieve sales targets.
● Develop a deep understanding of customer requirements, coordinate internal resources, and meet customer needs.
● Develop new clients and increase future sales potential.
● Collaborate with supporting departments to implement business contracts, technical standards, and framework agreements.
● Collect market information and competitor insights.

Main Challenges:

● Explore new customers and increase customer loyalty in new regions.
● Stay updated on market dynamics and industry changes to identify new opportunities.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher, preferably in an engineering-related discipline.
● 3+ years of B2B direct sales experience and 3+ years of experience in the medical device industry.

Personal Attributes:

● Proactive and self-driven. Excellent customer service mindset, with a background in interventional/implantable medical devices and knowledge of metal component products being preferred.
● Willingness to travel, with travel percentage exceeding 50%.

Job requirements

Job requirements

Role Description:

● Conduct research on new technologies related to medical device materials and components.
● Conduct feasibility studies on advanced medical device materials and components.
● Improve process technology in quality and performance aspects of medical device materials and components.
● Prepare technical and quality documents for medical device materials and components, including development materials, quality standards, and patents.

Main Challenges:

● Stay updated on cutting-edge technologies in the industry and promote the application of new technologies and materials.
● Integrate resources, drive project progress, and efficiently accelerate the incubation and production of new products and projects.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher in Polymer Materials, Metal Materials, Textile Materials, or related disciplines.
● 3+ years of product development experience in the field of implantable medical products.

Personal Attributes:

● Proficient in material processing knowledge.
● Fluent in English (listening, speaking, reading, and writing) with good communication, coordination, and organizational skills.

Job requirements

Job requirements

Role Description:

● Confirm and continuously improve processes.
● Handle product exceptions, analyze the reasons for non-conformities, and implement corrective and preventive measures.
● Design relevant product processes and raw materials, understand the process challenges, related risks, and control measures throughout the product realization process.
● Understand the main components of competing products based on product and market needs and propose product solutions.

Main Challenges:

● Optimize product stability and improve product quality.
● Cost reduction, efficiency improvement, new process development, and risk control.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher in Polymer Materials, Metal Materials, Textile Materials, or related disciplines.
● 2+ years of technical work experience, with 2+ years of experience in the medical or polymer industry.

Personal Attributes:

● Familiar with material processing technology, knowledge of Lean Manufacturing and Six Sigma, and the ability to improve product quality and achieve optimization.
● Strong communication and collaboration skills, independent problem-solving ability, continuous learning mindset, and ability to handle pressure.

Job requirements

Job requirements

Role Description:

● Quality control: Timely handle product quality exceptions and ensure product quality compliance (non-conformities, CAPA, material evaluation, measurement system analysis, process changes, process change quality control, risk management, quality traceability).
● Quality improvement and support: Assist in process validation and ensure the identification and evaluation of process change risks (change control, standard analysis, quality optimization, inspection optimization).
● Quality system and monitoring.
● Identify product quality risks and improvement opportunities, implement improvements, and ensure manageable product quality risks.
● Continuously seek methods to optimize product quality monitoring, improve the stability and reliability of quality monitoring methods.
● Other tasks assigned by superiors.

Main Challenges:

● Plan quality management programs and drive quality improvement based on product and production line development, aiming to enhance product quality.
● Continuously promote quality risk prevention, control, and improvement, improve incoming, in-process, and finished product quality, and reduce customer complaints.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher in Polymer Materials, Metal Materials, Textile Materials, or related disciplines.
● 5+ years of experience in the same role, preferably with a background in the medical device industry.

Personal Attributes:

● Familiarity with medical device regulations and standards, ISO 13485, experience in quality management for new projects, proficiency in FMEA and statistical analysis related to quality, adept at using quality tools, and familiarity with Six Sigma.
● Strong problem-solving, communication, and collaboration skills, time management, ability to handle pressure, mental and psychological maturity, and innovation capabilities.

Job requirements

Job requirements

Role Description:

● Market analysis: Collect and provide feedback on market information based on the company's market strategy, local market characteristics, and industry status.
● Market expansion: Develop sales plans, explore potential markets, identify customer needs, and provide solutions. Optimize sales plans based on market research and analysis to achieve sales targets.
● Customer management: Consolidate and summarize customer information, develop customer visit plans, and maintain customer relationships. Implement the signing of business contracts, confidentiality agreements, technical standards, framework service agreements, etc. Manage order delivery, payment schedules, and confirmations of goods export documents. Contact and follow up on post-sales issues.
● Marketing activities: Plan and participate in various marketing activities, such as relevant medical exhibitions, industry conferences, and key product promotion meetings.

Main Challenges:

● Cultural differences: Different countries and regions have diverse cultural backgrounds and values, which can result in variations in product positioning, marketing, and sales strategies. Understanding and adapting to the local culture is crucial for successful sales.
● Legal and regulatory issues: Different countries and regions have varying laws and regulations, particularly regarding trade, product standards, and intellectual property. You need to understand and comply with the applicable laws and regulations to ensure compliant operations.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or higher, preferably in Polymer Materials.
● Fluent English; knowledge of Spanish or Portuguese is preferred. Familiarity with the local medical device market environment. 5+ years of business development experience in the medical device or polymer material application field.

Personal Attributes:

● Ability to independently develop customers, negotiate, and communicate internally and externally with multiple parties.
● Proactive, team-oriented, and adaptable to business trips.

Job requirements

Job requirements

Role Description:

● Organize and operate the overall quality work in accordance with local laws and regulations. Establish the company's quality management system and ensure its compliance.
● Manage and improve quality effectiveness through regular checks and internal audit programs.
● Lead CAPA and complaint reviews, management reviews, and risk management development with the functional team. Monitor the quality compliance of overseas suppliers.
● Develop, implement, and maintain the quality management system (QMS) for the entire process control. Coordinate external and corporate audits and maintain quality management system certification.
● Verify components and final products during factory transfer to ensure adequate and effective product evaluation.
● Review SOPs to ensure compliance with regulatory requirements. Address related quality issues and assume responsibility for daily product quality release. Maintain an integrated documentation system and guide execution at each manufacturing site. Utilize data analysis skills to identify common risks/issues and provide solutions.
● Establish test methods, carry out method validation and verification, conduct laboratory testing, and ensure effective operation of the laboratory system.
● Arrange manpower for inspecting raw materials, semi-finished products, and finished products to ensure compliance with quality standards.
● Provide training, communication, and advice.

Main Challenges:

● Regulations and Compliance: The medical device industry is subject to strict regulations and compliance requirements. As a quality manager, you need to ensure that products comply with these regulations and standards and that company operations align with relevant requirements.
● Quality Control: Quality control is crucial in the medical device industry as product quality directly affects patient health and safety. You need to ensure that the company's quality management system operates effectively, including the ability to detect, assess, and resolve quality issues.
● Risk Management: Medical device manufacturing involves certain risks, including product failures, safety issues, and legal liabilities. As a quality manager, you need to effectively manage and mitigate these risks to ensure the company's reputation and interests are not compromised.

What We Are Looking For:

Education and Experience:

● Bachelor's degree or above in science and engineering. Advanced degree preferred.
● 7+ years of experience in quality-related roles, preferably in a manufacturing environment.

Personal Attributes:

● Familiarity with ISO 13485 quality system and regulatory standards such as FDA QSR 820 and Part 211.
● Experience in constructing quality system documents and conducting compliance audits.
● Strong presentation skills and experience as a trainer.
● Excellent interpersonal skills with a proven ability to effectively interact with multiple organizational units.
● Proficient in the application of quality tools such as FMEA, statistical analysis, process validation, etc.