Location: Laconia,NH, USA
The primary purpose of this position is to perform standardized measurements of parts in-process involving prescribed measurement tools under guided supervision. This position will work to maintain elements of Quality Management Systems (QMS) in accordance with ISO 13485 and FDA 21 CFR 820 requirements as well as company protocols.
* Shift Available: C-Shift (Thursday-Saturday 7:00am-7:00pm)
* Pay Range: $23.00 to $24.50 (Hourly base rate) + Shift differential
Benefits:
* New employees are eligible for the following benefits effective date of hire!
* Medical, dental, and vision benefits
* Company-paid life insurance and disability benefits
* Generous Paid time off and 10 paid Holidays
* 401k Plan with Company Match
* Tuition Reimbursement
* Voluntary Universal Life and Long-Term Care
* Voluntary Legal Plan
* Pet Insurance
* Home Ownership Program
Main Job Responsibilities:
* Primarily performs incoming or in-process inspection of raw materials and components for conformance to specifications such as dimensions, tolerances, and other purchase order requirements.
* May perform visual and functional in-process, and final inspection of devices or labels.
* Utilize mechanical and optical inspection equipment to measure components and devices to verify product meets specification.
* Utilize quality procedures, specifications, work instructions, and associated documents in the performance of inspection duties.
* Identify and process nonconforming material in accordance with established procedures.
* Provide quality assurance support within the organization as experience and time allow.
* Writing and preparing inspection reports regarding inspection and testing results
* Other duties may be assigned
Basic Requirement:
* High School Diploma or equivalent
* Experienced in Microsoft office suites (excel, word, power point, outlook)
* Solid experience with quality systems documents
* Strong organizational skills with proven ability to complete multiple tasks simultaneously
* Strong understanding of FDA CFR 820, ISO 13485
Job Experience:
* Minimum 2 years of quality assurance experience or machine operations experience with in-process inspection exposure in a manufacturing environment required.
Physical Requirements:
* Exerting up to 50 pounds of force occasionally, and/or up to 10 pounds of force frequently, and/or lift, carry, push, pull, or move objects.
Skills/Competencies:
* Ability to communicate and work with those inside and outside the department, handle multiple assignments and prioritize accordingly.
* Demonstrated attention to detail
* Basic understanding of blueprint reading, inspection equipment and sampling plans
* Basic machine shop math (fractions to decimals and metric conversion)
* Ability to follow appropriate department policies, procedures and practices.
* Positive teamwork attitude.
* Good problem solving skills.
* Good writing and verbal skills.
* Understanding of Lean Manufacturing philosophies
#INDHP
Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.
Other details
* Pay Type Hourly
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* Laconia, NH, USA