Job summary
Job post source
This job is directly from Nitto Denko Corporation
Job overview
The Quality Control Analyst II at Nitto Denko Corporation is responsible for conducting routine and non-routine analyses of materials and products to ensure compliance with cGMP guidelines, impacting product quality and safety.
Responsibilities and impact
The role involves conducting various routine tests, analyzing samples timely according to project plans, reviewing data for compliance with specifications and GMP regulations, generating stability reports, assisting in developing procedures and protocols, revising documentation, and providing training to other analysts.
Experience and skills
Candidates need a BS in chemistry, biology, or related fields with 2-5 years of QC analyst experience in a GMP environment, and familiarity with analytical testing equipment like HPLC, Karl Fischer, Spectrophotometry, and 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
Position your resume to emphasize your hands-on experience with routine and non-routine analytical testing, particularly under cGMP guidelines, showcasing familiarity with HPLC, Karl Fischer, Spectrophotometry, and LCMS techniques.
Highlight your ability to review data for compliance with specifications and GMP regulations, as well as your experience generating stability reports and contributing to SOP and testing procedure development.
Apply through multiple channels including Nitto Denko Corporation’s official corporate careers page and LinkedIn to maximize your application’s visibility.
Connect with current QC analysts or team members in the quality control division at Nitto Denko Corporation on LinkedIn; use ice breakers such as commenting on recent advancements in analytical methods or asking about their experience working with cGMP processes.
Optimize your resume for ATS by incorporating keywords from the job description such as 'cGMP', 'HPLC', 'stability reports', 'SOP development', and 'analytical testing equipment' to ensure it passes automated screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application platforms, and find relevant LinkedIn contacts to network with, allowing you to focus your time on interview preparation and skill enhancement.
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