This role will offer you:

• Opportunity to join one of the leading companies within the intraocular lens technology space.

You will be responsible for:

• Develop, validate new analytical procedures in accordance with USP, ICH, AOAC and ISO requirements.
• Trouble-shoot problems associated with analytical methods for lens components, including raw materials, finished product method development, quantitative and qualitative analysis, and improvement of analytical methodologies.
• Act as R&D liaison to Regulatory Affairs responsible for defining and supplying technical information on products to Regulatory Affairs for regulatory submissions.
• Be responsible for maintaining and expanding analytical capabilities of the department.

You will bring the following:

• A Ph.D. degree in Analytical Chemistry, Toxicology, Pharmaceutical Sciences, or a related discipline is a prerequisite for this role. The candidate should ideally possess 7-10 years of experience in the pharmaceutical industry, or a combination of industry experience and postgraduate research.
• Hands-on proficiency in various chromatography methods such as HPLC, GC, GCMS, GPC, as well as spectroscopic methods including UV, FTIR, and NMR, is essential.