Quality Associate at TMC
Gand, , Belgium -
Full Time


Start Date

Immediate

Expiry Date

26 Jul, 25

Salary

0.0

Posted On

26 Apr, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Regulations, Continuous Improvement, Manufacturing Processes, Regulatory Requirements, Preventive Actions, Preparation, Pharmaceutical Industry, Operational Activities, Training Programs, Root

Industry

Pharmaceuticals

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
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