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Quality Control Inspector Jobs

Company

PBS Biotech

Address Camarillo, CA, United States
Employment type FULL_TIME
Salary
Category Internet Publishing
Expires 2023-08-24
Posted at 9 months ago
Job Description
GENERAL PURPOSE


The Quality Control Inspector is responsible for measuring, recording, and releasing product in-process and to finished goods inventory. Using visual, mechanical, and optical gauging instruments in accordance with Standard Operating Procedures and other documents as required, such as work orders, drawings, and QC data sheets.


Responsibilities


Essential functions of the job are listed below. Other responsibilities may also be assigned. Please note that the essential functions may vary depending on department size, organizational structure and/or geographic location. Reasonable accommodations may be made to allow differently-abled individuals to perform the essential functions of the job.


Primary Responsibilities


  • Communicate to supervisor in a timely manner, of:
  • Perform inspections of product labeling per approved artwork/specifications.
  • Perform sampling and inspection of incoming materials and components per procedures, specification documents, statistical sample plan (eg, AQL), using inspection tools such dimensional measurement, vision systems, and visual inspection.
  • Strong knowledge of interpreting drawings, customer specification, test methods, and inspection criteria.
  • Perform inspections for assembled products per procedures and complete related documentation and approvals.
  • Release product to next location upon completion within MRP system.
  • Independently handle problems that arise within area of responsibility.
  • Tool and/or equipment malfunctions.
  • Maintain complete, legible, and accurate records.
  • Ability to change priorities when directed by Supervisor/Manager.


Minimum Qualifications


The following are the minimum qualifications that an individual needs in order to successfully perform the duties and responsibilities of this position. Please note that the minimum qualifications may vary based upon the department size and/or geographic location.


Knowledge/ Experience


  • 3-5 years of experience in a Quality role for medical products in a regulated environment. Eg, medical device, single use medical or biopharma products, or similar field.
  • Or 5+ years experience working in a quality system that requires a high degree of quality control, ideally GMP quality system, Medical device (QSR/ISO13485), aerospace (AS9100), and/or ISO 9001.


Skills/ Abilities Pertinent To This Position


  • Entry-level computer knowledge (Excel, Word, Outlook)
  • Ability to follow written specifications and procedures
  • Ability to be flexible in changing daily workload priorities as directed
  • Ability to meet standards for quality and quantity
  • Ability to work in a team environment
  • Ability to accurately perform detailed production inspection work
  • Ability to read and interpret drawings and specifications
  • Use of small inspection tools (i.e. calipers, micrometers, rulers)
  • Ability to accurately completed documentation of work performed
  • Ability to adhere to standards for labeling and segregation of materials
  • Ability to communicate effectively orally and in writing, with coworkers, supervisors, and other employees


PHYSICAL DEMANDS


In general, the following physical demands are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to allow differently-abled individuals to perform the essential functions of the job.


Must be able to operate in a clean room and in a production environment as described in procedures. Must be able to see, hear, speak and write clearly in order to communicate with other employees; manual dexterity required for occasional reaching and lifting of small objects. Must be able to lift various weights up to 50lbs as needed to meet job requirements.


WORK ENVIRONMENT


In general, the following conditions of the work environment are representative of those that an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to allow differently-abled individuals to perform the essential functions of the job within the environment.


This role is performed in a production or lab-like environment. Occasionally exposed to moving mechanical parts, fumes, machine lubricants, airborne particles, vibration, and risk of electrical shock, high noise while in the manufacturing plant. Personal protective equipment (vision and hearing) used in plant. Exposed to heat, humidity conditions during warm weather months.


Pay Range:


$21.63 - $28.84


NXTThing RPO is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.


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