Nitto Denko Corporation

Quality Control Analyst III, Raw Material

MILFORD, MAPosted 23 days ago

Job summary

  • Job post source

    This job is directly from Nitto Denko Corporation

  • Job overview

    The Quality Control Analyst III, Raw Material role at Nitto Denko Corporation involves performing routine and non-routine analyses of raw materials and products to ensure quality compliance under cGMP guidelines, impacting product quality and safety.

  • Responsibilities and impact

    The analyst will test and analyze samples, review analytical data for compliance, assist in developing experimental procedures, revise documentation, and provide training and guidance to other analysts.

  • Experience and skills

    The position requires a BS/MS in chemistry, biology or related field, 4-7 years of QC analyst experience in a GMP environment, and familiarity with analytical equipment like HPLC, Karl Fischer, Spectrophotometry, and possibly LCMS.

Company overview

Nitto Denko Corporation is a Japanese multinational company specializing in the development and production of high-performance materials, including adhesive tapes, optical films for displays, and medical products. Founded in 1918, the company has evolved from producing electrical insulation materials to becoming a global leader in diverse industries such as electronics, automotive, healthcare, and environmental solutions. Nitto generates revenue by providing innovative products and solutions to businesses worldwide, leveraging its expertise in polymer synthesis and material science. Key milestones include its pioneering role in polarizing films for LCDs and its ongoing commitment to sustainability and technological advancement.

How to land this job

  • Tailor your resume to emphasize your experience with analytical testing equipment such as HPLC, Karl Fischer, UVNIS, IR, NMR, and LCMS, highlighting your proficiency in performing routine and non-routine analyses under cGMP guidelines.

  • Showcase your ability to review analytical data for compliance and your role in developing or revising SOPs, testing procedures, and material specifications, as these are critical responsibilities for this position.

  • Apply through multiple channels including Nitto Denko Corporation’s official corporate careers page and LinkedIn to maximize your application’s reach and visibility.

  • Connect with current QC Analysts or team members in the quality control division at Nitto Denko on LinkedIn; start conversations by asking about their experience with cGMP compliance or recent projects involving raw material analysis to break the ice.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'cGMP,' 'HPLC,' 'analytical testing,' 'SOP development,' and 'QC analyst' to improve your chances of passing automated screenings.

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