Quality Assurance Specialist (f/m/d)

at  FREUDENBERG GROUP

Elmshorn, Schleswig-Holstein, Germany -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate14 Aug, 2024Not Specified15 May, 20245 year(s) or aboveEnglish,Food IndustryNoNo
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Description:

Working at Freudenberg: We will wow your world!

Responsibilities:

  • Examination and release of raw materials and finished products according to physico-chemical parameters as well as sensory and microbiological tests.
  • Evaluation and documentation of analytical results and initiation of appropriate corrective measures
  • Preparation and review of certificates of analysis, test plans and reports
  • Monitoring of test equipment
  • Preparation of work instructions and documentation
  • Participation in the maintenance of the QM system as well as certifications and standards
  • Documentation and monitoring of CCPs

Qualifications:

  • Completed vocational training as a chemical laboratory assistant, chemical-technical assistant or comparable qualification.
  • 5 years of professional experience in a manufacturing company in the food industry
  • Good knowledge of the relevant product safety standards
  • Sound SAP knowledge in the QM module
  • Confident handling of MS-Office
  • Good knowledge of English
  • Very careful, systematic and independent way of working

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.
Capol Gmb

Responsibilities:

  • Examination and release of raw materials and finished products according to physico-chemical parameters as well as sensory and microbiological tests.
  • Evaluation and documentation of analytical results and initiation of appropriate corrective measures
  • Preparation and review of certificates of analysis, test plans and reports
  • Monitoring of test equipment
  • Preparation of work instructions and documentation
  • Participation in the maintenance of the QM system as well as certifications and standards
  • Documentation and monitoring of CCP


REQUIREMENT SUMMARY

Min:5.0Max:10.0 year(s)

Other Industry

Pharma / Biotech / Healthcare / Medical / R&D

Other

Trade Certificate

Preparation and review of certificates of analysis test plans and reports

Proficient

1

Elmshorn, Germany