Jost Chemical Co.
  • 03-Jun-2022 to 03-Jul-2022 (CST)
  • Quality Assurance
  • St. Louis, MO, USA
  • Full Time

Quality Assurance Plant Compliance Auditor

We're seeking ambitious, hard-working talent for the Jost Quality 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 in order 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 Plant Compliance Auditor

Position: Full time

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.
  • Up to a 4% Discretionary Match (like a profit-sharing contribution) to your 401k.
  • Paid Time Off (PTO) Employees eligible after 90 days of continuous 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.


Primary Responsibilities

  • All aspects of quality assurance compliance in a fast paced manufacturing environment
  • Ensure procedures are actively being followed
  • Enforce Good Manufacturing Practices and Good Documentation Practices in the plant
  • A high level of attention to detail and quality
  • Prompt ability to act on deficiencies
  • Inform colleagues of GMP deficiencies in a diplomatic manner and works towards solutions
  • Spearhead improvements of deficiencies found and follow up on improvements
  • Maintain a thorough audit log of deficiencies
  • Follow through with corrective and preventative actions (CAPA) on deficiencies and maintain thorough documentation of CAPA information
  • Opportunities for growth in process investigations, training, batch record review, production tracking, and similar QA functions

Knowledge 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

Education Requirements

  • Primary preference for Bachelor's Degree in Chemistry, Chemical Engineering, or Biochemistry, Bachelor's Degree in the general sciences also acceptable.

Exempt

Jost Chemical Co.
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