Manufacturing Technician II (AM Swing Shift)
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At a glance
Job overview
Nitto Denko Corp. is hiring a Manufacturing Technician II (AM Swing Shift). The Manufacturing Technician II is responsible for implementing assigned production operations within defined schedules in a cGMP environment. This role involves maintaining a clean work environment, following safety procedures, completing GMP documentation, and participating in investigations. The technician will also identify and implement small continuous improvement projects and ensure compliance with training before performing operations.
Key focus areas include Maintain a clean and organized work environment, Follow GMP and safety cultures, procedures, and regulations, and Identify and submit safety hazards and incidents.
Successful candidates bring High School Diploma Or Equivalent With College Level Chemistry Degree Or Equivalent Work Experience and 2+ Years cGMP Manufacturing Experience. Important skills include GMP, Safety Cultures, Problem Solving, Process Understanding, Documentation Understanding, and Identify Abnormal Results. Preferred (not required): Review Documentation, Revise Procedures, Participate In Investigations, and Execute CAPA Tasks.
Skills & qualifications
Skills
Qualifications
Full job description
About this opportunity :
As a Manufacturing Technician II, you'll be responsible for the implementation of assigned production operations working within defined production schedules in a cGMP environment. This is a swing shift position which runs from 8:00 AM - 8:00 PM (1st week M,T and F - Sn / 2nd week W-Th). This role comes with a 5% shift differential.
Key Responsibilities:
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Maintain a clean and organized work environment. Responsible for following GMP and safety cultures, procedures, and regulations.
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Identify and submit safety hazards and incidents.
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Complete GMP documentation in a compliant manner. May review less complex documentation like logbooks.
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May revise procedures under direct supervision.
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May participate in investigations. May execute CAPA tasks.
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Identify and implement small continuous improvement projects.
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Responsible for assigned production activity and ensuring training is compliant prior to performing operations.
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Problem solving: basic understanding of process and documentation. Ability to identify abnormal results and report to higher position.
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Proficient in the assigned area of the process.
Required Skills/Abilities:
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Minimum education requirements: high school diploma or equivalent with college level Chemistry degree or equivalent work experience.
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A biotechnology certificate or college degree is preferred.
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Must have knowledge of basic laboratory instrumentation such as use of pH meter, UV instrumentation, and solution delivery systems (process skids).
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Two plus years of experience in cGMP manufacturing environment. Performance/other experience can be considered pending manager discretion.
The annualized salary range for this roles is $61,700.00 - $75,600.00.
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