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Job Location drjobs

India

Monthly Salary drjobs

INR INR 1800000 - 2200000

Vacancy

1 Vacancy

Job Description

Position: Inspector I Weekend Shift 4
Location: Southington CT 06489
Duration: 10 Months
Job Type: Contract
Work Type: Onsite
Shift: Thursdays and Fridays 10:45 PM to 7:15 AM Saturdays and Sundays 6:45PM to 7:15 AM
Job Description:
Qualifications
Knowledge and Skills
  • Basic computer skills in order to regularly access and document information.
  • Must have basic written and oral communication skills adequate to communicate with other team members understand verbal instructions and read and comprehend written work instructions including words and engineering drawings.
  • Ability to perform inspection tasks using microscopes calipers and micrometers. Ability to complete 1015 inspections.
  • Demonstrated knowledge of medical device regulations and FDA regulatory standards preferred.
  • Minimum Qualifications Education and Experience
  • High School graduate or GED equivalent. AA or Technical Degree preferred.
  • Must be 18 years of age.
Work Environment
  • Must be able to perform essential job functions in an office environment.
  • Long periods of sitting to enter/ analyze data is expected.
  • Must have adequate manual dexterity to operate standard office equipment.
  • Must be able to occasionally lift objects up to 25 lbs.
  • Typically requires travel less than 5% of the time.
Responsibilities
Position Summary
  • This is a Night/Weekend position with the work schedule as follows: Thursdays and Fridays 10:45 PM to 7:15 AM / Saturdays and Sundays 6:45PM to 7:15 AM
  • The Inspector I will be responsible for the performance of entry level inspection repetitive tasks associated with visual inspections and basic functional testing knowledge.
  • Ensure company products are in compliance with internal and external specifications by performing a variety of routine and nonroutine inspections and evaluations.
Essential Duties & Responsibilities
  • Perform accurate mechanical physical and visual inspections of raw materials components and subassemblies as per inspection plans and specification requirements.
  • Follow all procedural requirements in the area of responsibility in order to maintain compliance to applicable Quality System Regulations (i.e.: cGMP compliance).
  • Support the paper document archival process including preparation as well as the scanning of Documents for electronic archival.
  • Initiate NonConformance reports as required.
  • Supports NC and CAPA activities as needed.
  • Work on special projects as they may arise.

knowledge of medical device regulations,regulations,compliance,microscopes,communication,assemblies,basic computer skills,fda regulatory standards,instructions,skills,inspection tasks,written and oral communication,micrometers,calipers

Employment Type

Full Time

Company Industry

Key Skills

  • Edp
  • Desktop Support
  • CAD
  • E Learning
  • Cardiac Anesthesia
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