At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?
This role is part of Alcon's Project Management function, a team that ensures all regular and one-off projects are planned, organized, and executed effectively to help our people and the world see brilliantly.
The Manager I, Manufacturing/Engineering Project Management (Professional Path), is primarily responsible for leading projects within the Manufacturing facility, enhancing project performance and operational efficiency. You will guide projects from start to finish, including planning, budgeting, and scheduling, while leading the project team. Specifics include:
Lead and manage cross-functional project teams, overseeing technical design, equipment setup, process implementation, business systems, and regulatory approvals.Develop and execute detailed project plans, including scope, scheduling, budgeting (Capital & Expense), and resource allocation.Coordinate and communicate with internal and external stakeholders, including vendors and suppliers, to meet project objectives related to cost, quality, and delivery.Actively identify, assess, and mitigate project risks to ensure successful outcomes.Provide clear reporting to site management, including progress updates and performance tracking.Support the development and documentation of engineering project processes, technical specifications, SOPs, and templates.Manage improvement, transfer, or equipment-related projects to ensure timely delivery and compliance with standards and regulatory requirements.Conduct feasibility studies and provide recommendations for effective technology transfers and new equipment installations.
What Can You Bring to Alcon:Bachelor’s degree in Science or EngineeringMinimum 7 years of relevant experience in project or engineering management, ideally in a manufacturing environmentStrong command of English (both spoken and written)Proven experience leading multiple cross-functional projectsHands-on experience in budget management and capital project trackingStrong leadership, collaboration, and problem-solving skillsProficiency in Microsoft Office (Excel, Word, PowerPoint)Experience in the medical device or pharmaceutical industry is a plusFamiliarity with project management software (e.g., Poggio or equivalent) is a plusPMP (Project Management Professional) certification is a strong advantage
Why Join Us:Opportunity to work with a leading global medical device company.Collaborate with a diverse and talented team in a supportive work environment.Competitive compensation package and comprehensive benefits.Continuous learning and development opportunities.
At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before.Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
Responsibilities:Ensure adequate raw materials for production to prevent stockouts.Coordinate with vendors and logistics teams for timely material delivery.Work closely with the Production Planning team, Manufacturing, and QC Incoming team to highlight any supply issues impacting the production plan.Provide rolling forecasts of raw materials to suppliers as required.Generate accurate weekly inventory reports and dispatch them to relevant parties in a timely manner.Monitor and expedite critical raw materials to prevent shortages.Assist in material collection and provide shipment mode information (by air or ocean).Perform additional tasks as assigned by the supervisor.
What Can You Bring to Alcon:Bachelor’s degree holder.Strong understanding of material planning.Good understanding of SAP ERP is preferred.Excellent communication skills.Proficiency in English.Strong data analysis skills.Strong project and time management abilities.Effective problem-solving skills.
Why Join Us:Opportunity to work with a leading global medical device company.Collaborate with a diverse and talented team in a supportive work environment.Competitive compensation package and comprehensive benefits.Continuous learning and development opportunities.
At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.
As a Senior Validation Engineer supporting the Manufacturing Team, you will be trusted to work at the Batam Plant. The candidate will be supporting and executing the validation/ qualification activities for Processes, Equipment, Computerized Systems, Utilities, Facilities and Cleaning Procedures.In this role, a typical day will include:Execute and support site validation/qualification activitiesSupport Validation Efforts for Tech Transfer projectsPreparation, review and remediation of validation protocolsTraining of validation protocols, site validation SOPsSupport validation activities for large capital procurement projectsEnsure compliance and provide technical support to the validation team
WHAT YOU’LL BRING TO ALCON:
Bachelor’s Degree in Science or Engineering5 - 10 years experience in manufacturing/ manufacturing science & technology/quality / technical development in medical device, pharmaceutical manufacturing or food & beverage manufacturingAt least 5 years of experience in executing validation activities in complex projectsGood understanding of requirements and validation lifecycleFluent in English and local languageStrong ability in reviewing and writing technical reports
At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us?
This role is part of Alcon's Engineering function, a team focused on improving quality, processes, products, packaging and materials across our business to help deliver brilliant outcomes. The Sr. Associate, Packaging Engineering, is primarily responsible for designing and developing product packaging, including creating new solutions and enhancing existing ones. You will test materials, support prototype development, and apply advanced technical knowledge and analytical skills.
Packaging Design & DevelopmentDesign, develop, and optimize packaging systems (pouches, blister trays, cartons, labels, boxes, shrink wraps, etc.) to meet functional, quality, and regulatory requirements.Conduct material evaluation, testing, and selection with consideration for compatibility, sustainability, manufacturability, durability, and cost.Lead or support root‑cause investigations and implement improvements for packaging-related performance issues.
Prototyping & Process DevelopmentLead or contribute to prototype design, assembly, testing, and line trials to validate new packaging concepts.Develop and refine packaging manufacturing processes, including equipment specification, qualification, and validation.Collaborate closely with Engineering, Operations, Quality, Regulatory, and Supply Chain to ensure smooth technology transfer to production.
Equipment, Systems & AutomationOversee installation, commissioning, operation, and maintenance readiness of packaging machinery and inspection systems (e.g., vision systems, inline verification).Troubleshoot equipment or system performance and drive corrective and preventive actions to maintain efficiency and quality.
Quality, Compliance & Risk ManagementIntegrate quality assurance and control requirements into packaging and process design.Ensure adherence to technical standards, regulatory guidelines, and global packaging/labelling regulations.Perform or support risk assessments (pFMEA, QRA) for packaging components and processes.Follow GxP, SOPs, and documentation requirements to ensure full traceability and audit readiness.
Artwork & LabellingCreate, review, and manage product artwork within the Artwork Management System.Ensure labelling accuracy and regulatory compliance across all markets.Support change control processes related to artwork, packaging, and labelling updates.
Continuous Improvement & LeadershipIdentify and implement improvements in packaging robustness, sustainability, cost, and manufacturability.Make informed technical decisions within your area and contribute to broader project and organizational objectives.
WHAT YOU’LL BRING TO ALCON: Bachelor’s degree or higher in Packaging Engineering, Mechanical Engineering, Materials Science, Industrial Engineering, or related technical field.5+ years of experience in packaging engineering, ideally within medical device, pharmaceutical, or other regulated manufacturing environments.Strong understanding of packaging materials (plastics, films, foils, paperboard, adhesives) and their performance characteristics.Hands‑on experience with packaging equipment, automation systems, and vision/inspection systems (preferred).Working knowledge of equipment qualification and process validation (IQ/OQ/PQ), as well as design controls.Experience with CAD tools and engineering documentation (drawings, specifications, BOMs).Familiarity with Artwork Management Systems and labelling compliance requirements.Knowledge of GxP, ISO 11607, FDA 21 CFR Part 820, EU MDR, and other relevant regulatory frameworks.Ability to perform risk assessments (FMEA, QRA) and apply quality control methodologies.Proficiency with statistical tools (e.g., Minitab) is a plus. Excellent communication skills, with the ability to explain technical concepts to diverse stakeholders.Detail‑oriented, proactive, and committed to high standards of quality and compliance.
Why Join Us:Opportunity to work with a leading global medical device company.Collaborate with a diverse and talented team in a supportive work environment.Competitive compensation package and comprehensive benefits.Continuous learning and development opportunities.
