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 the Sr. Associate, Chemical Production Operations, you will be responsible for the improvement of routine and non-routine processes in Chemical Production. Provide scientific, engineering and validation support to Chemical Production Operations Team. Work with Subject Matter Experts (SMEs) from Alcon Research and Development (R&D) and Manufacturing and Technical Operations (MTO) for new product and process transfers (as required). Execute validations in accordance with AML procedure and in compliance with current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs) and applicable guidelines.
In this role, a typical day will include:
Drive initiatives / execute projects to improve system performance, safety and compliance in Chemical ProductionMain contributor in Technology Transfer project (if any); delivering results within the projected timeline and budgetPerform equipment commissioning, qualification and process validation for new equipment and processes including revalidation of existing validated equipment and processes in Chemical ProductionPerform periodic CSA related activities such as, but not limited to, User Access Review, Audit Trail Review etcCertified Investigator. Conduct non-conformance investigations including follow-through on the implementation and effectiveness of all identified CAPAsPerform other duties as assigned
WHAT YOU’LL BRING TO ALCON: At least five (5) years of working experience in a pharmaceutical, medical device or high-volume manufacturing environment with minimum 2 years of validation experience.Has sound technical problem-solving skills, good communication skills,Computer literacy in MS OfficeGood understanding of GMP, GDP and other relevant standards / requirements
HOW YOU CAN THRIVE AT ALCON:Join a global leader with a rich history of innovation and excellence in eye care. Be part of a collaborative and supportive team culture that values diversity and inclusion. Enjoy a competitive compensation package and opportunities for career advancement. Make a meaningful difference in the lives of patients worldwide by contributing to cutting-edge advancements in eye health.Alcon CareersSee your impact at alcon.com/careers
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 Associate, Operational Excellence under our Business Excellence Dept, you will get to work in cross functional collborations in driving continuous improvement throughout the whole site and managing site CAPEX projects.
In this role, a typical day will include
1. Project Management:- Manage and monitor progress of site CAPEX projects and maintain accurate reporting and documentation.- Perform CAPEX cash flow forecasting, monitoring and preparation of monthly reports.- Ensure compliance of site project management practices with Alcon Financial Control Manual (AFCM) and Alcon Manual of Accounting (AMA) requirement.- Provide regular update of site CAPEX projects status to site leadership team and key stakeholders and highlight identified risk/ issue.- Provide support for site or corporate audits related to Assets under Construction (AuC) and project management areas.2. Operational Excellence:- Drive site Continuous Improvement initiatives and culture through Lean and Six Sigma training, Kaizen program, and other initiatives.- Coordinate Lean and Six Sigma activities, data collection, reporting, and analysis.- Facilitate Value Stream baseline exercise and workshop, to identify process bottleneck and actions plan.3. Others:- Support preparation, submission, reporting, audit, and follow up for government grants related to projects.- Adhere to Alcon standards, such as quality, ethical, health, safety, and environment (HSE),and information security standards.
WHAT YOU’LL BRING TO ALCON:
Degree in Engineering or related scientific fieldMin 2 years of experience in GMP environmentLean six sigma Green Belt highly preferred
HOW YOU CAN THRIVE AT ALCON:Join a global leader with a rich history of innovation and excellence in eye care.Be part of a collaborative and supportive team culture that values diversity and inclusion.Enjoy a competitive compensation package and opportunities for career advancement.Make a meaningful difference in the lives of patients worldwide by contributing to cutting-edge advancements in eye health.Alcon CareersSee your impact at alcon.com/careers
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 the Sr. Associate, Mechanical Equipment Engineering, you will be responsible for leading equipment performance, OEE, reliability, and qualification activities to support manufacturing operations. You will lead equipment and process improvements, performance qualification/validation activities, and ensure compliance with medical device regulatory requirements while collaborating closely with Engineering, Quality, Operations, and global stakeholders.
In this role, a typical day will include: Drive continuous improvement initiatives to improve equipment performance and manufacturing efficiency.Implement modifications or upgrades to meet evolving requirements.Lead cost‑reduction and productivity improvement projects.Troubleshoot equipment issues and implement corrective/preventive actions (CAPA).Lead equipment readiness, qualification, and validation activities.Develop qualification documentation for medical‑device regulatory expectations.Actively participate in discussions - speak up and challenge assumptions to drive decisions.Work collaboratively across teams to meet yield, cost, and cycle‑time targets.
WHAT YOU’LL BRING TO ALCON: Bachelor’s Degree in any relevant engineering field with strong competency in mechanical, electrical, and/or automation systems3-5 years in regulated manufacturing environment, experience in medical device manufacturing preferred but not a mustStrong experience in equipment design & qualification activities (IQ/OQ/PQ).Proven record driving improvement initiatives.Hands‑on troubleshooting and optimization capability.Strong analytical and problem‑solving skills.Familiarity with FMEA, SPC, root‑cause analysis.Able to provide standby support to 24/7 operations
HOW YOU CAN THRIVE AT ALCON:Join a global leader with a rich history of innovation and excellence in eye care. Be part of a collaborative and supportive team culture that values diversity and inclusion. Enjoy a competitive compensation package and opportunities for career advancement. Make a meaningful difference in the lives of patients worldwide by contributing to cutting-edge advancements in eye health.Alcon CareersSee your impact at alcon.com/career
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?
Responsibilities:
The Senior Manager, Data Privacy, APAC role is responsible for the development, implementation, maintenance, and adherence to the organization's privacy and technology law program -Collaboration with legal counsel and management, key departments, and committees to ensure organization has and maintains appropriate privacy and confidentiality consent, authorization forms, and information notices and materials reflecting current organization and legal practices and requirements -Information privacy risk assessments -Compliance monitoring activities in coordination with the organization's other compliance and operational assessment functions -Development of corporate privacy policies and procedures for the handling of protected health information. In this role, you will lead complex projects, using your advanced skills and experience to achieve objectives and enhance project performance. Specifics include:
• Manage the development and maintenance of privacy policies and procedures for handling protected health information (PHI)• Conduct regular privacy risk assessments and assist with privacy audits to ensure compliance• Work closely with legal counsel to develop and review consent forms, authorization forms, and information notices• Monitor privacy compliance and collaborate with departments to address privacy-related issues and concerns• Coordinate with cross-functional teams to integrate privacy practices into operational processes• Track developments in privacy regulations and ensure compliance with local, national, and international privacy laws• Develop and maintain privacy-related training programs for employees to ensure understanding and compliance
Education: Degree from an accredited law school or reputable institution of higher education.
Skills & Experience:Admitted to practice law in one jurisdiction relevant for Asia-Pacific practice10 years legal experiences including at least 5-year prior working experiences working in-house multinational companiesPrior APAC exposure, strong understanding of APAC privacy, data protection and data security laws, technology laws including AI and Cybersecurity related regulations.Experienced in handling privacy inquiries, complaints and incidents.Prior in-house experience with a multinational healthcare company for business partner role is not a must but is preferredThis is an individual contributor role, ideal for someone with strategic business partnering mindset and hands-on experience.Detail-oriented self-starter who can handle multiple matters on a timely basis.Solid interpersonal skills and proven ability to communicate complex issues in a clear and succinct manner.Able to learn new things quickly. Well-organized and capable of handling workload in a complex matrix Organisation.Visa sponsorship/relocation not authorized.
Why join Alcon?- Join a global leader with a rich history of innovation and excellence in eye care.- Be part of a collaborative and supportive team culture that values diversity and inclusion.- Enjoy a competitive compensation package and opportunities for career advancement.- Make a meaningful difference in the lives of patients worldwide by contributing to cutting-edge advancements in eye health.
If you're ready to take the next step in your career and lead a dynamic team towards success, we want to hear from you! Apply now and join us in shaping the future of eye care at Alcon.
Alcon CareersSee your impact at alcon.com/careers
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in any employment practices. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If you need a reasonable accommodation for any part of the application process, please send an email to alcon.recruitment@alcon.com.
As an Microbiology Subject Matter Expert you are tasked to Site SME in microbiological and sterility assurance, environmental monitoring program and cleanliness control strategies. Manage and lead a team of Micro QC Lab associates to perform inspection and testing of products to meet quality standard.
JOB SCOPE
A Subject Matter Expect (SME) of Microbiological and Sterility Assurance test who will need to actively network with the internal and external scientific, technical and establish regulatory community to maintain state of the art knowledge.Establish company policy and developing company strategies with respect to cleanliness, sterilization, clean rooms, pure water systems and related areas.Provide micro-SME support to the site and assist in new product development and provide input in the design of manufacturing processes, water systems, controlled environments, and packaging from a microbiological standpoint.Have responsibility for the site environmental monitoring program and cleanliness control strategies.Work with cross-functional team to establish, validate and maintain clean manufacturing environments, processes, and utilities.Issue, conduct NCR and OOS investigation as a certified investigator, identify root cause and determine appropriate CAPA.Responsible for compliance to applicable Quality RegulationsLead a team of Microbiology associates and ensure microbiology inspection and testing activities are executed in compliant to SOP and regulatory requirements.Provide direction and supervision to direct reports.Lead and execute continuous improvement initiatives to improve productivity, efficiency, and cost optimization.Support internal and external audits and is responsible for audit finding closure, as required.
REQUIREMENT
Min Degree in MicrobiologyMin 8 Years of experience in Microbiology lab and 3-5 years in a supervisory role in a manufacturing environment, preferably in medical or pharmaceutical field
About the Role:
As a Site Regulatory Associate, you will be responsible for authoring and maintaining Chemistry, Manufacturing, and Controls (CMC) documentation to support global and local regulatory submissions. You will collaborate closely with global and country Regulatory Affairs (RA) teams, ensuring timely filings, managing regulatory queries, and assessing the impact of manufacturing and quality changes. This role is critical in bridging site operations with global regulatory strategies, ensuring compliance while enabling innovation.
Key Responsibilities :
Author and review CMC sections of regulatory dossiers.
Support new product filings, variations, renewals, and lifecycle management submissions.
Partner with global RA teams to align submission strategies and timelines.
Coordinate with country RA affiliates to meet local regulatory requirements.
Manage responses to Health Authority queries, liaising with site experts and QA.
Conduct regulatory impact assessments for site changes and support change control processes.
Maintain compliance with evolving global regulatory guidelines (ICH, EMA, FDA, PMDA, WHO).
Support audits and inspections with regulatory documentation and expertise.
Drive continuous improvement in submission processes and site regulatory compliance.
Skills & Competencies :
Strong knowledge of global CMC regulatory requirements and guidelines.
Excellent technical writing and documentation skills.
Ability to interpret complex technical data and translate into regulatory language.
Strong collaboration and communication skills across global and local teams.
Proficiency in regulatory submission systems (eCTD tools, Veeva Vault, or similar).
Analytical mindset for change impact assessments and risk evaluation.
Ability to manage multiple projects under tight timelines.
Qualifications :Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or Life Sciences.10 + years of experience with recent 3–5 years in Regulatory Affairs (CMC focus) within the pharmaceutical industry.Experience with global regulatory submissions and country-specific filingsFamiliarity with manufacturing processes, quality systems, and GMP requirements.
