Product Steward - Surgical

Perusahaan : Id01 Pt. Ciba Vision Batam Company

Jenis Pekerjaan : Full-Time

Batam, Riau Islands

Jumlah Pelamar

000+

Lamar Sekarang

Deskripsi Pekerjaan - Product Steward - Surgical

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 Product Steward Engineer, you will own the process knowledge of the product(s) assigned throughout the commercial lifecycle, oversight on product capability through data trending and statistical analysis of product quality attributes. Responsible for process capability monitoring, to ensure process(s) are robust and product in continued state of validation and continuously improving.

In this role, a typical day will include:

Monitoring product performance using SPC.

Identify opportunity of improvements and Implementing new or revised or improved production processes for the efficient/economical mass production of goods including IOLs and /or surgical consumables.

Doing assigned projects to mitigate material/ manufacturing related issues.

Reducing manufacturing related issues using risk management tools (like pFMEA of mfg. Processes).

Conducting tests throughout all stages of production to determine control over applicable variables and troubleshooting/solving production problems

Ensuring that production processes and procedures are in compliance with regulations.

WHAT YOU’LL BRING TO ALCON:

Experience in process support role on the shop floor of pharmaceutical / medical device manufacturing and/or QA/QC.

Understand basic investigation / root cause analysis tool.

Understand concept of DMR/MDF/pFMEA related to medical device mfg process.

Proven process understanding (Medical Device/Pharma, GMP, Regulatory aspects).

Statistical Expert: Data handling and applied statistics is a must.

Technical report writing skill in English and local languag.

English communication skills and proficient in site local language