Quality Associate - Life Sciences

at  TMC

Ghent, Vlaanderen, Belgium -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate09 Oct, 2024Not Specified09 Jul, 2024N/AContinuous Improvement,Pharmaceutical Industry,Regulations,Preparation,Manufacturing Processes,Preventive Actions,Training Programs,Regulatory Requirements,Operational Activities,RootNoNo
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Description:

Belgium Life Sciences Ghent On-site
Looking to drive continuous improvement and ensure quality standards in the pharmaceutical industry? Join us as Quality Associate!
About The Member Company

We are a global high-tech consultancy company with a team of entrepreneurial engineers, scientists, and digital experts from around the world. Together we form a fast-growing and proud community. We offer consultancy services to high-profile clients globally in diverse service areas, such as:

  • Technology & Engineering
  • Energy & Renewables
  • Life sciences & Pharma
  • Digital & IT

Responsibilities:

  • You ensure that the manufacturing processes comply with the GMP regulations.
  • You develop, implement and maintain quality systems such as QMS, QCS, and SOPs to ensure the consistent production of high-quality products.
  • You conduct risk assessments and perform root cause analysis, striving for continuous improvement
  • You develop and manage corrective and preventive actions (CAPA’s).
  • You develop and conduct training programs to ensure operational activities comply with the quality systems and regulations.
  • You provide support in preparation for regulatory inspections and audits and ensure that all quality records are accurate and up-to-date


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

IT Software - Other

Clinical Pharmacy

Graduate

Proficient

1

Ghent, Belgium