Shift Quality Control Analyst

at  Huntsman

Duxford, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate13 Jul, 2024Not Specified13 Apr, 2024N/AGood communication skillsNoNo
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Description:

Job Description:
Shift Quality Control Analyst
Role Overview:
Huntsman is currently recruiting for a Shift Quality Control Analyst position at our chemical manufacturing site in Duxford. The successful candidate will play a crucial role in ensuring adherence to quality standards, conducting thorough testing of manufactured products, and providing essential support to maintain operational excellence. The selected candidate will join our team on a 12-month fixed-term contract contributing to the resilience and efficiency of our Quality Control department in anticipation of increased demand. This role operates on a rotating 3-shift pattern Monday to Friday. The person will report to the Quality Team Leader.
Do you think you’re the right fit for this opportunity? Apply today!

Role Responsibilities:

  • Conduct in-process and final testing of manufactured products following designated test methods and procedures.
  • Validate, maintain, and calibrate laboratory testing equipment.
  • Perform re-life testing as required and support testing queries related to customer complaints.
  • Notify Production and Quality management of non-conforming products.
  • Provide advice to the manufacturing plant on routine in-process failures.
  • Accurately log all quality testing data into the QC database/LIMS and SAP.
  • Properly file retained samples/paperwork and maintain an in-date supply of product standards.
  • Participate in gauge R&R/round robin testing.
  • Assist with customer/auditor visits.
  • Aid process development with investigations and new product testing as needed.
  • Assist with quality inspections and audits of the Production plants.
  • Inspect, record, and file CoA results for specified incoming raw materials.
  • Adhere to company standards and regulatory EHS guidelines.

Experience and Competencies:

What we are looking for:

  • BTEC/NVQ 3/HND in Laboratory Science preferred.
  • Previous professional experience in a laboratory environment is required.
  • Preferably, experience in the chemical industry; however, candidates with relevant experience in other industries will be considered.
  • Working knowledge of Quality Control processes.
  • Proficiency in English.
  • Good IT proficiency required to operate LIMS, QC database, and SAP.
  • Ability to work with minimum supervision.
  • Excellent team player with strong building relationship skills.
  • Excellent organizational and communicational skills.
  • Ability to deal with ambiguity and prioritize tasks.
  • Proactive attitude, quality focused, performance focused, conscientious approach.

About Us:
Huntsman Corporation is a publicly traded global manufacturer and marketer of differentiated chemicals with 2015 revenues of approximately $10 billion. Our chemical products number in the thousands and are sold worldwide to manufacturers serving a broad and diverse range of consumer and industrial end markets. We operate more than 100 manufacturing and R&D facilities in approximately 30 countries and employ approximately 15,000 associates within our 5 distinct business divisions. For more information about Huntsman, please visit the company’s website at
www.huntsman.com
.
What next?
If you would like to join an innovative, collaborative and multicultural team, please apply now. Your application will be forwarded to a Talent Acquisition Partner, who will strive to get back to you as soon as they can. We understand that applying for a new job is a big decision and we will work hard to keep you updated and support you along the way.
Additional Locations:

Responsibilities:

  • Conduct in-process and final testing of manufactured products following designated test methods and procedures.
  • Validate, maintain, and calibrate laboratory testing equipment.
  • Perform re-life testing as required and support testing queries related to customer complaints.
  • Notify Production and Quality management of non-conforming products.
  • Provide advice to the manufacturing plant on routine in-process failures.
  • Accurately log all quality testing data into the QC database/LIMS and SAP.
  • Properly file retained samples/paperwork and maintain an in-date supply of product standards.
  • Participate in gauge R&R/round robin testing.
  • Assist with customer/auditor visits.
  • Aid process development with investigations and new product testing as needed.
  • Assist with quality inspections and audits of the Production plants.
  • Inspect, record, and file CoA results for specified incoming raw materials.
  • Adhere to company standards and regulatory EHS guidelines


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Proficient

1

Duxford, United Kingdom