Production Engineer - 18 months contract

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 responsible for preparing, updating, and maintaining production documentation including Work Instructions, rework instructions, NCRs, ECNs, and production records. You will ensure all documentation is accurate, controlled, and aligned with manufacturing processes to support efficient and compliant production.

You will work closely with engineering, production, and quality teams to translate technical requirements into clear, structured, and user-friendly documentation for the production floor. The role also supports ongoing updates driven by engineering changes, non-conformances, and process improvements.

They will:

• Develop a broad understanding of the Alcon products, their underlying technologies, and their application at Alcon.

• Assist in meeting any product-based objectives set by Engineering, Production, Quality, Regulatory, and Marketing.

• Work collaboratively across all disciplines to take products from development to mass production and general availability in the market.

• Analyse new and existing engineering technologies and apply them in the testing of manufactured products.

Key responsibilities include:

  • Prepare and maintain Work Instructions, rework instructions, and technical documentation

  • Support NCR and ECN processes through accurate documentation updates

  • Translate complex engineering requirements into clear, practical instructions

  • Ensure documentation meets quality and controlled environment standards

  • Work with Bills of Materials (BOMs), production records, and traceability systems

  • Collaborate with Production Engineering, Quality, and Operations teams

  • Contribute to continuous improvement of documentation and production processes

Skills & Experiences:

  • Engineering degree (Mechanical, Manufacturing, Biomedical, or similar)

  • Experience in medical device or controlled manufacturing environments (e.g. ISO 13485, GMP, cleanroom)

  • Proven proficiency in Microsoft Office applications, particularly Word and Excel

  • Demonstrated track record of producing clear, accurate, and timely documentation in a fast-paced manufacturing environment

  • Strong experience working with NCRs, ECNs, Work Instructions, and rework documentation

  • Proven ability to prepare and maintain technical documentation, including work instructions, process documentation, and production records

  • Experience working with Bills of Materials (BOMs) and production traceability systems

  • Ability to interpret engineering drawings and translate complex technical requirements into clear, practical instructions

With Attributes:

  • Excellent written communication — able to move between technical detail and clear, simple instructions

  • Methodical and well-organised, with strong attention to detail

  • Practical and action-oriented approach to supporting production

  • Confident working with cross-functional teams in a fast-paced environment


•Full-Time Role: Standard day shift with stable hours.

•18 months contract with potential to permanent

No visa sponsorship / relocation will be provided for the role. All applicants need to have full Australian work rights.

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.

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