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Merrimack Manufacturing

Production Inspector- 1st Shift

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What they do

A Quality Inspector inspects and evaluates products according to company quality control standards. Inspects goods or packaging in a production or manufacturing facility.

$48,251 / year median in New Hampshire

+6% projected growth

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Job Description

Production Inspector- 1st Shift Merrimack Manufacturing - 2.3 Manchester, NH Job Details Full-time 1 day ago Qualifications Precision assembly Full Job Description
COMPANY OVERVIEW
Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life.
POSITION OVERVIEW
This position will perform various functions in ensuring production processes run efficiently and effectively. They must have excellent attention to detail, be self-sufficient in assembly, testing and documentation of mechanical and electrical assemblies. The Production Inspector will know all processes and procedures on the line and be able to monitor workers and the efficiency of the line.
RESPONSIBILITIES
Evaluate Inspecting equipment for safety and functionality Ensure that products and goods manufactured meet quality standards obtainable in the industry Check finished products to ensure quality, and that industry standards are met before they are declared ready for use Keep records of Inspection performance Work as middleman between workers and management to create healthy communication Follow and contribute to Inspection schedule for the execution of projects in a timely manner Ensure that work materials are present when needed. Maintain neat, orderly and clean work area to ensure efficiency and no safety hazards. Participate in safety programs, meetings, and trainings as required. Bring safety concerns to the attention of management. Participate in continuous improvement activities as part of a cross-functional team. Maintain Inspection Area integrity by using proper attire and adherence to Quality practices and procedures as applicable. Adhere to general safety rules, manufacturing procedures, company policies and procedures, ISO, QSR, and FDA regulations.
QUALIFICATIONS AND SKILLS
Minimum of 3 years hands-on experience in a manufacturing environment (preferred). Experience with assembly, testing and the documentation of mechanical and electrical devices Possess excellent interpersonal skills and ability to relate effectively with all members of the team from various backgrounds Strong verbal and written communication skills to effectively relate with team members and the management Willingness to undertake various tasks and adapt to unexpected situations within dynamic company environment Medical device manufacturing experience preferred Working knowledge of Microsoft Office and basic computer skills. Good hand eye coordination and manual dexterity required Willingness to attend leadership trainings and any other trainings that management determines valuable to a lead's role Other assignments as assigned by management
EDUCATION
H.S. Diploma or GED. 2LNCO520uZ