Director, Manufacturing Science & Technology Engineering
Listed on 2026-10-16
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Engineering
Quality Engineering -
Quality Assurance - QA/QC
Quality Engineering
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 Director, MS&T, you will lead site's MS&T organization, which is responsible in ensuring products are in an industry standard validated state and related technical knowledge is maintained. Maintain and improve the scientific oversight of the manufacturing processes and technical changes. Owner of product's lifecycle manufactured at the site.
In this role, a typical day will include:- a. Ensure that departments execute and maintain the Site Master Validation Plan (SVMP) activities in their respective scope of responsibility, including annual revalidation / re-qualification and cleaning validations.
- b. Provide governance / directions on site's validation activities.
- c. Ensure validation requirements are in alignment with regulatory expectations.
- a. Ensure robust product stewardship for all products and end-to-end technical oversight of manufacturing processes at all stages of their commercial lifecycle.
- b. Undertake product remediation of technical issues with clear interfaces with Quality Operations, Manufacturing (Production, Engineering, etc) and Research and Development.
- c. Support excellence in manufacturing through standard setting and technical capability development and deployment.
- d. Ensure technology strategies are in line with current and future standards in partnership with key functions.
- e. Manage product / process risk management and knowledge management through process Failure Mode Effect Analysis (pFMEA)
- f. Process Support/Control and Continuous Monitoring
- g. Provide and analyse product-specific manufacturing data and provide results to Technical Review, Product Quality Review and Management Review.
- h. Track CM parameters and monitor all critical / key variables as appropriate for the assigned product(s), such as Critical Process Parameters, In Process Control parameters, Product Quality Attributes, Characteristics of raw materials. etc) using statistical analysis and conducting regular product specific data trending.
- i. Lead / provide assistance in technical deviation investigation, robust CAPA and relevant follow-up on product / process related investigations, which include complaints, OOE, OOS, etc
- a. Product launch and transfer governance transfers.
- b. Ensure that all product / process transfers, including 2nd Sourcing projects are all validated and according to timelines.
- Technical Transfer Right First Time
- On Time Review / Approval of Technical Transfer Documents
- Validation Right First Time
- Reduce Risks of Product Recalls
- Continuous Improvement Projects and Cost Improvement Projects
- No critical or major observations during audits/inspections
- Minimum 10-15 years of experience in new manufacturing site start-up, validation, technology transfer, and new product introduction activities within the medical device industry,…
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