Nitto Denko Corporation

Quality Assurance Specialist II, Batch Records Raw Materials

MILFORD, MAPosted 30+ days ago

Job summary

  • Job post source

    This job is directly from Nitto Denko Corporation

  • Job overview

    The Quality Assurance Specialist II role at Nitto Denko Corporation supports QA operations by reviewing batch records and raw materials to ensure compliance with cGMP and regulatory standards, acting as a key quality interface between operational teams and quality oversight.

  • Responsibilities and impact

    The specialist reviews and approves raw material documentation, manages quality records, uses SAP for material release, coordinates corrections, supports inspections and audits, communicates across departments, and contributes to continuous improvement and inspection readiness.

  • Experience and skills

    Requires a BS/BA in science or equivalent with at least 2 years of experience in Production or Quality Assurance, strong decision-making in batch record review, and ability to communicate effectively across QA and operational departments; must be able to gown and enter manufacturing suites.

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 batch record review, raw material release, and compliance with cGMP practices, as these are central to the Quality Assurance Specialist II role at Nitto Denko Corporation.

  • Highlight your proficiency with quality documentation management, including Certificates of Analysis, SAP system usage for material release/rejection, and coordination with cross-functional teams such as Manufacturing, Supply Chain, and Quality Control.

  • Apply through multiple platforms including Nitto Denko's corporate careers page and LinkedIn to maximize your application visibility and ensure your resume reaches the right hiring managers.

  • Connect with current employees in the QA or Operations divisions at Nitto Denko on LinkedIn; initiate conversations by referencing recent company news, asking about their experience with QA operations, or expressing genuine interest in how they maintain cGMP compliance.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'batch record review,' 'raw material release,' 'cGMP compliance,' 'SAP,' and 'quality documentation management' to ensure it passes automated screenings.

  • Use Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and find relevant LinkedIn contacts to network with, allowing you to focus your time on preparing for interviews and follow-ups.

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