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)
Nebo zkus mobilní apku
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Naskenuj kód
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