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 Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly. The Sr. Associate, Quality Control Lab - Microbiology, is primarily responsible for conducting routine testing and tasks in the Microbiology Laboratory, ensuring compliance with quality systems, safety guidelines, and documentation processes. You will support product release, maintain trained staff, and foster collaboration with other departments.
In this role, a typical day will include:Leading the Microbiology Laboratory, ensuring smooth operations, and implementing GMP/GLP/GDP and SOPs.Demonstrating competence in laboratory methods and investigational techniques, validation of laboratory procedures, and validation support of processes outside the laboratory, validation of laboratory procedures, and validation support of processes outside the laboratory.Ensuring safety and data integrity in the laboratoryImplementing Good Laboratory Practices and investigating OOS resultsEnsuring all testing equipment is qualified and maintained.Managing equipment qualification and method validationDelivering projects on time and assisting with budget preparationAccountable for HSE implementation and activities in the department
WHAT YOU’LL BRING TO ALCON:Bachelor's degree in Microbiology/Biology with a focus on MicrobiologyMinimum 5 years of experience in the medical or pharmaceutical industry with microbiology laboratory exposureHands-on experience in water monitoring, product bioburden, endotoxin testing, and media preparationStrong leadership skillsSolid understanding of Environmental Monitoring and microbial staining and identificationExperienced in cleanroom and compressed air systems managementHands-on experience in managing technical writing for NCR request
HOW YOU CAN THRIVE AT ALCON:Good team playerPart of growing companyOpportunity be involved and exposure to projects from global site
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.
Job Description
As a Senior Validation Engineer II supporting the Manufacturing Team, you will be trusted to work at the Batam Plant. The candidate will be will be leading a team of Validation Engineers for the Tech Transfer project in the validation/ qualification activities for Processes, Equipment, Computerized Systems, Utilities, Facilities and Cleaning Procedures.
In this role, a typical day will include:Write the validation plan including complex process validationsReview validation/qualification written by the Validation EngineersPreparation, review and remediation of validation protocolsTakes a leadership role in the project team and project managementCommunicates with the project team, site management and global project stakeholdersWill visit the transferring site to learn the process and become receiving site expertExpected to have an expert level of understanding of validation and strong project management skills
WHAT YOU’LL BRING TO ALCON: Bachelor Degree in Science or EngineeringWith a minimum of 8 years experience in manufacturing/ manufacturing science & technology/quality / technical development in medical device or pharmaceutical manufacturingExperience in complex projectsExperience leading a team of Validation EngineersDeep understanding of Process Validations and Validation typesStrong understanding of requirements and regulations of FDA, ISO, etcFluent in English and local languageStrong ability in reviewing and writing technical reportsThis role will be required to travel
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'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 Supply Chain function, a team that manages the logistics, inventory management, and supply chain analytics for Alcon's industry leading products to ensure products are delivered efficiently and effectively so that people can see brilliantly.
The Sr. Manager, Strategic Sourcing (Management Path), is primarily responsible for leading strategic sourcing initiatives and managing supplier relationships to optimize performance and achieve business goals. You will guide teams, implement departmental plans, and ensure successful procurement strategies.
Specifics include:Develop and execute strategic sourcing strategies that deliver cost savings, ensure continuity of supply, and introduce competitive alternative suppliersApply data analytics to identify trends, uncover opportunities, and initiate new sourcing projectsManage site budgeting, spend variance analysis, and project coordination in partnership with the cross-functional teamLead negotiations to secure supply of direct materials—metal, electronics, molded components—and support material and capital equipment localization effortsBuild and present business cases to the Director, COE and senior leadership to gain alignment on localization strategies and sourcing initiatives
WHAT YOU’LL BRING TO ALCON:Bachelor’s Degree or equivalent experienceStrong English communication skills (verbal and written)Minimum 8 years of relevant experienceProven relationship‑building capabilities across internal teams and external partnersDemonstrated expertise in Direct Materials (injection molding, devices, metals, chemicals)Strong analytical skills; proficiency in Excel with exposure to SAP, Power BI, Alteryx, and PowerPointExperience developing and executing global strategic sourcing strategiesTrack record of managing regional and global RFPsStrong negotiation skills involving complex supply agreements and third‑party engagementsAbility to perform scenario modeling, business case development, and total cost of ownership (TCO) assessmentsComfortable navigating ambiguity while driving results with clarity and focus
HOW YOU CAN THRIVE AT ALCON:Good team playerPart of growing companyOpportunity be involved and exposure to projects from global site
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?
We are seeking a highly experienced and technically proficient Control Automation Principal Engineer to lead the design, implementation, and optimization of automation systems within our medical device manufacturing operations, and in compliance with regulatory standards (e.g., FDA, GMP). This role requires a blend of deep technical expertise, strategic thinking, and strong leadership to drive innovation, ensure operational excellence, lead cross-functional project teams, and driving digital transformation initiatives.
The Principal I, Automation & Control Engineering, is primarily responsible for leading technical projects in the design, development, and maintenance of instrument/electrical and automation control systems. You will apply mathematical modeling, analyze dynamic behavior, and use control theory to ensure optimal system performance.
In this role, a typical day will include:Lead the development, integration, and lifecycle management of automation and control systems (PLC, SCADA, DCS) in GMP-regulated environments.Oversee automation projects from concept through commissioning, ensuring alignment with quality and compliance standards.Act as technical liaison with global engineering teams and external vendors to ensure seamless implementation of smart technologies (i.e. auto inspection system, etc.)Collaborate with cross-functional teams including Quality Assurance, Validation, IT, and Manufacturing to ensure seamless system integration.Ensure all automation systems meet regulatory requirements (21 CFR Part 11, GAMP 5, Data Integrity).Lead investigations and root cause analysis for automation-related deviations and implement corrective actions.Evaluate and implement new technologies (e.g., PAT, IIoT, digital twins) to support continuous improvement and Pharma 4.0 initiatives.Develop and maintain SOPs, validation protocols, and technical documentation.Mentor and guide junior engineers and technicians in automation best practices.
WHAT YOU’LL BRING TO ALCON:Bachelor’s or Master’s degree in Electrical Engineering, Automation, Mechatronics, or related field.Minimum 10 years of experience in automation engineering, with at least 5 years in the pharmaceutical or life sciences industry.Deep knowledge of PLCs (e.g., Siemens, Allen-Bradley), SCADA/HMI systems, and industrial communication protocols.Strong understanding of GMP, GAMP 5, 21 CFR Part 11, and data integrity principles.Proven track record of leading complex automation projects in regulated environments.
Preferred Qualifications:PMP or equivalent project management certification.Experience with MES, batch control (ISA-88), and data historians (e.g., OSIsoft PI).Familiarity with cybersecurity standards for control systems (ISA/IEC 62443).Experience with validation and qualification of automation systems (IQ/OQ/PQ).
Leadership & Soft Skills:Demonstrated leadership in cross-functional project teams.Strong communication and stakeholder management skills.Ability to influence and drive change across departments.Strategic mindset with a hands-on approach to problem-solving.
HOW YOU CAN THRIVE AT ALCON:Good team playerPart of growing companyOpportunity be involved and exposure to projects from global site
If you're passionate about automation, compliance, and innovation in medical device manufacturing, we'd love to hear from you. Apply now to be part of a forward-thinking team driving excellence in medical device industry!
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.
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 Associate II, Manufacturing Science & Technology Engineering - Materials Engineer, is primarily responsible for developing, implementing, and evaluating new production materials, equipment, and technologies. You will conduct research, perform feasibility tests, and collaborate with vendors and partner functions, requiring advanced technical knowledge and problem-solving skills. Specifics include:
Develop the planning and execution of material testing, feasibility studies, and qualification processes for alternate sources and new materials.Conduct technical feasibility assessments and support supplier capability and readiness evaluations.Develop, implement, and evaluate new production materials, equipment, and technologies prior to mass production to optimize quality and cost.Generate protocols and comprehensive reports related to feasibility studies, engineering studies, and material qualifications.Coordinate and oversee protocol execution and ensure alignment with internal and external stakeholders.Work closely with vendors and suppliers to define specifications, ensure timely delivery, and maintain cost-efficiency.Collaborate with cross-functional teams such as R&D, Quality, and Commercial to integrate new materials and processes into production.Perform manufacturing R&D to resolve production challenges, reduce costs, and ensure compliance with quality standards.Develop and implement standard manufacturing procedures and evaluate processes for continuous improvement.Ensure all activities are in compliance with HSE, GMP, data integrity, and company policies.Take ownership of decision-making in your project scope and actively contribute to regulatory compliance and organizational success.
WHAT YOU’LL BRING TO ALCON:Min Degree in science or engineering studiesGood understanding of injection molding, tubings , extrusion related processes would be advantageous but not a must0-2 Years of relevant experience in material testing, training will be provided
HOW YOU CAN THRIVE AT ALCON:Good team playerPart of growing companyOpportunity be involved and exposure to projects from global site
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 Training & Development function, a team that enhances employee skills, knowledge, and performance to align with the company's strategic goals and help our people and the world see brilliantly.The Associate I, Manufacturing & Technical Operations Training (Professional Path) is primarily responsible for supporting productivity and product quality through operational tasks, troubleshooting, and continuous improvement projects. You will ensure training aligns with Quality and Production needs, providing On-The-Job Training and Performance Observation.
Specifics include:Organize and implement learning programs that support alignment with company values, skills expectations, and operational needs.Evaluate training effectiveness through feedback, assessments, and performance metrics.Promote a continuous learning culture through campaigns, knowledge-sharing, and self-directed learning initiatives.Review training documents before GxP submission and collaborate with the Training Coordinator on lesson planning.Support data collection for TNA, including training history and skill matrix updates; prepare templates and compile feedback.Manage day‑to‑day training schedules, send invitations, set up venues/online tools, and handle logistics.Assist in organizing and executing onboarding programs to ensure a smooth and timely learning experience.Distribute, collect, and track training evaluation results; highlight low scores or recurring issues.Maintain and organize employee training site records in compliance with standards and audits.
WHAT YOU’LL BRING TO ALCON:Diploma or Bachelor’s Degree in any field (preferably Communications, Psychology, or Technology Education)Open to fresh graduates; experience in organizing events or committees is a plusGood command of EnglishProficiency in Microsoft OfficeExperience with Canva or similar design tools is an advantage
HOW YOU CAN THRIVE AT ALCON:Good team playerPart of growing companyOpportunity be involved and exposure to projects from global site
