Jost Chemical Co.

Quality Assurance Inspector I Jobs at Jost Chemical Co.

Quality Assurance Inspector I Jobs at Jost Chemical Co.

Sample Quality Assurance Inspector I Job Description

Quality Assurance Inspector I

Quality Assurance Inspector I

Jost Chemical is seeking ambitious, hard-working talent for the Jost Quality Assurance Team!

Are you looking for a career at a fast-paced environment, where your hard work and dedication will pay off? Are you a team player, who sets goals to get the job done and would like to use your skills to grow with a great company?

Then, this position is right for you!


Quality Assurance Inspector I

Position:

Our offer:

  • Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance after 60 days.
  • 3% Safe Harbor contribution to your 401k.
  • Paid Time Off (PTO) Employees eligible first day of employment.
  • 9 Company Paid Holidays (72 hours) each year.
  • Uniforms Provided
  • Foot Protection- annual allowance for all laboratory, maintenance and production employees.
  • 24-hour access to our free, on-site fitness center.
  • We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work.

Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry.


Quality Assurance Inspector I

Education Requirements

  • High School Diploma or GED acceptable

Primary Responsibilities

  • All aspects of quality assurance compliance in a fast paced manufacturing environment
  • Ensure procedures are actively being followed
  • Support Good Manufacturing Practices and Good Documentation Practices in the plant
  • A high level of attention to detail and quality
  • Prompt ability to act on GMP observations
  • Inform colleagues of GMP improvements
  • Maintain a thorough audit log of GMP improvement opportunities
  • Follow through with corrective and preventative actions (CAPA) on GMP program compliance
  • Act as liaison and educator to quality compliance and continuous improvement

Knowledge & Experience Requirements

  • GMP from a pharmaceutical and/or food safety perspective
  • Good Documentation Practices
  • Good Manufacturing Practices
  • Good understanding of scientific methods and technical/mechanical processes
  • FDA ICH-Q7 and 21 CFR 117 environment

Ability to:

  • Work in extreme cold and hot (120 F) environment
  • Comprehend oral and written English instruction
  • Follow established policies and procedures
  • Exhibit manual dexterity, perceptual speed and extent flexibility
  • Adopt to rapidly changing priorities based on business needs
  • Pass pre-employment physical with drug screen and physical capabilities test

Position Details

  • Reports to QA Compliance Supervisor
  • Full time position

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