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Senior Manufacturing Engineer

1 month ago

Batam, Riau, Indonesia Alcon Full time

Direct message the job poster from Alcon

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.

Senior Manufacturing Engineer is responsible to lead cross-functional teams, including but not limited to Production, Quality, MS&T, & Engineering to improve manufacturing efficiency, safety on work environment, product quality, non-conformance investigation, and CAPA.

Responsibilities:

  • Identify, lead, and manage improvement projects related with productivity and material efficiency to meet business objectives by utilizing Lean Six Sigma concept.
  • Optimize manufacturing process, ensuring efficiency and quality standards are met.
  • Understand the failure/non-conformance investigation requirements based on International Standards, GMP/QSR US FDA, and ISO Standards.
  • Responsible to diagnose problems, perform investigation and developing CAPA on related production issue.
  • Collaborate with cross-functional teams, internal and / or external, to develop plans for improving production productivity, quality, cost, and safety.
  • Implement Quality Control measures within Manufacturing Processes.
  • Responsible and accountable to ensure full compliance.
  • HSE implementation and performance in Production Department. Provide support in area process responsibility for other HSE activities that are assigned by Management.

What Can You Bring to Alcon:

  • Degree in Engineering, Science, or relevant field
  • At least 5 years of experience
  • Proficient in English both verbally and written.
  • Experience in material and productivity efficiency, process improvement, and continuous improvement
  • Good understanding of GMP/QSR US FDA, and ISO Standards.
  • Strong analytical and investigative skills.
  • Green belt certified is a plus.

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.
Seniority level

Mid-Senior level

Employment type

Contract

Job function

Engineering and Manufacturing

Industries

Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Manufacturing

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