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Compliance manažer / Manažer pro dodržovaní předpisů

Méně než 2 týdny

CONFITEX TECHNOLOGY

Nasobůrky 162, Litovel

Vzdálenost od tebe uvidíš po zadání adresy ve výpisu nabídek.


Plat

70 000 - 100 000 Kč hrubého

Úvazek

Práce na plný úvazek

Smlouva

Pracovní smlouva

Vzdělání

Vysokoškolské / univerzitní

Jazyky

Čeština (Výborná) nebo Angličtina (Výborná)

Zařazené

Quality and quality control, Manufacturing and industry, Technology and development, Auditor, Inspector, Project Manager, Regulatory specialist, Quality director/manager


O pozici

Job Description: Compliance Manager

Location: Litovel, Czechia

Company: Confitex Technology
Reports to: Operations Manager – E.U.
Job Level: Senior
Employment Type: Full-Time, On-Site

Role Summary

  • Confitex Innovation Technology seeks a detail-oriented, experienced Compliance Manager for our manufacturing facility in Litovel, Czechia.
  • The ideal candidate will ensure full regulatory compliance with applicable standards for medical devices such as ISO 13485, MDSAP, MDR, CE, Oeko-Tex Standard 100, STeP by Oeko-Tex and other relevant industry certifications.
  • This is a senior role with critical responsibilities tied to product safety, quality assurance, and international compliance.

Key Responsibilities

  • Ensure ongoing compliance with ISO 13485, MDSAP, MDR, CE, Oeko-Tex Standard 100, STeP by Oeko-Tex, and other related regulatory frameworks.
  • Ensure compliance with local authorities including fire safety and health standards
  • Develop, implement, and manage quality and compliance programs across manufacturing processes.
  • Conduct internal and external audits, develop CAPAs, and drive process improvements.
  • Coordinate with certification bodies and regulatory agencies as needed.
  • Train staff on compliance procedures and quality standards.
  • Monitor and report key compliance metrics to senior leadership.
  • Support product and process documentation to meet market regulations.
  • Collaborate across departments to drive a culture of quality and compliance.

Qualifications and Requirements

  • Minimum 3-5 years experience in medical devices class 1 compliance
  • Experience in ISO 13485, MDSAP, MDR, CE, Oeko-Tex Standard 100, STeP by Oeko-Tex, or other relevant compliance programs
  • Strong knowledge of quality systems, audits, and regulatory frameworks.
  • Fluent in Czech and English; other language proficiency is an advantage.
  • Excellent communication, organizational and analytical skills.
  • Ability to work independently and as part of a team.

Salary and Benefits

The role offers a competitive annual gross salary in the range of CZK 70 000 – CZK 100 000 per month depending on experience. Benefits include:

  • Opportunities for professional growth and certification support
  • 20 days paid annual leave, will be increased to 25 days after 2-3 years
  • Participation in industry conferences and trade shows
  • Standard Czech employee benefits (meal vouchers, health care contributions and other)

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