Co-director Técnico (co-dt) – Analista Quality Assurance (fixed Term Contact)

med-in.at

Hybrid
Gmp compliance management
Product release documentation review
Tad regulatory platform usage
The position of Co-Director Técnico (Analista Quality Assurance) at med-in.at seeks a qualified professional to oversee quality assurance processes in the pharmaceutical industry. The role requires a strong background in GMP compliance and collaboration across departments, with a focus on continuous improvement

Job Summary

  • The role focuses on releasing finished products and managing regulatory submissions through the TAD electronic platform.
  • Candidates must ensure site compliance with cGMP standards and manage quality systems including change control and supplier management.
  • This hybrid position requires a Pharmacy degree and at least two years of experience in pharmaceutical quality assurance or control.

Matching Summary

Match Score: 85

The position of Co-Director Técnico (Analista Quality Assurance) at med-in.at seeks a qualified professional to oversee quality assurance processes in the pharmaceutical industry. The role requires a strong background in GMP compliance and collaboration across departments, with a focus on continuous improvement.

Skills & Requirements

Must-have

  • GMP compliance management
  • Product release documentation review
  • TAD regulatory platform usage
  • Change control system execution
  • Supplier quality management
  • Deviation investigation processes

Nice-to-have

  • Continuous improvement initiatives
  • Cross-departmental collaboration skills
  • Project support capabilities
  • Risk assessment expertise
  • Effective communication abilities

Key Requirements

  • University degree in Pharmacy (mandatory)
  • Minimum 2 years pharmaceutical industry experience
  • Intermediate to high English proficiency
  • Knowledge of GMP and GLP norms

Work Rights

Not specified

Tailored Resume

Cover Letter