Search the 5 jobs at Alcon

Responsible for ensuring the design transfer and manufacturing operation activities of medical devices meet quality and regulatory requirements. Supports program management and operations through all phases of medical products' lifecycle. Conducts investigations, reviews validation protocols, provides quality oversight, and supports audits.

Manage and direct all Quality Assurance and Quality Control activities at a manufacturing facility, ensuring compliance with regulations and standards. Responsible for Quality Management System implementation, training, and continuous improvement. Oversee product compliance, disciplinary actions, and interface with authorities. Manage budget, headcount, and quality management programs. Lead people development and project management activities.

As a Senior Executive supporting Quality Systems at Alcon, responsibilities include quality compliance, GxP training, record management, monitoring key performance indicators, identifying improvement opportunities, meeting quality objectives, coordinating activities, performing investigations, leading audits, and overseeing training activities. Degree in any engineering and minimum 7 years of relevant experience required.

The IOL Specialist at Alcon is responsible for achieving target sales of in-line products within designated territories. Responsibilities include delivering performance plans, increasing product usage, preparing business plans, improving knowledge of products, and identifying key opinion leaders. The ideal candidate should have at least 2 years of sales experience in the medical device industry, good interpersonal skills, and a positive attitude.

As a Quality Engineer at Alcon, you will ensure the design transfer and manufacturing operations of medical devices meet regulatory standards. Responsibilities include product release support, validation protocol approval, quality oversight, audit support, and performance monitoring. Desired qualifications include a degree in Science or Engineering, 1-3 years of QA/QC experience in the pharmaceutical and medical device industry, knowledge of regulatory standards, and strong communication and problem-solving skills.