Auditors, Technical & Clinical Experts — MTIC Group
- Location
- Lugano Paradiso
- Contract
- other
- Posted
- 45 days ago
Role overview
Job Application If interested, send your Curriculum Vitae to [email protected] ## Job Description MTIC InterCert of the MTIC Group is constantly and solidly growing in all areas of Certification, particularly as a Notified Body (CE 0068) for the Certification of Medical Devices.
For expansion of staff and for the opening of a new office in Emilia Romagna, we are looking for Technical Experts, Lead Auditors and Auditors for Conformity Assessment activities of Medical Devices pursuant to Regulation (EU) 2017/745.
The activities will include both the evaluation of technical documentation and audits of the Quality Management System (QMS), including audits according to EN ISO 13485.
This opportunity is exclusively reserved for candidates residing in Italy.
Work location: Rho/Emilia Romagna ##
- Requirements ### Product Reviewer / Final Reviewer
- Degree in engineering or chemical sciences or pharmacy
- Minimum 4 years of work experience with a medical device manufacturer, of which at least 2 years as a product reviewer with Notified Bodies
- Solid knowledge of Regulation (EU) 2017/745 and Directive 93/42/CEE (MDD)
- Solid knowledge of the main horizontal harmonized standards, including but not limited to ISO 14971, ISO 10993 series, EN 62366
- English language skills
- Preferable knowledge of MDR codes: MDA 0201, 0202, 0303, 0306, 0307, 0311, 0312, MDN 1102, 1201, 1202, 1203 ### Auditor
- Degree in engineering or chemical sciences or pharmacy
- Minimum 4 years of work experience with a medical device manufacturer
- Solid knowledge of Regulation (EU) 2017/745 and Directive 93/42/CEE (MDD)
- Solid knowledge of the main horizontal harmonized standards, including but not limited to ISO 13485, ISO 14971
- English language skills
- Lead Auditor training course according to ISO 19011 (40 hours) will be a preferential title ## Contact If interested, send your Curriculum Vitae to [email protected]
Contacts
- Job Application If interested, send your Curriculum Vitae to [email protected]
- Job Description MTIC InterCert of the MTIC Group is constantly and solidly growing in all areas of Certification, particularly as a Notified Body (CE 0068) for the Certification of Medical Devices.
- For expansion of staff and for the opening of a new office in Emilia Romagna, we are looking for Technical Experts, Lead Auditors and Auditors for Conformity Assessment activities of Medical Devices pursuant to Regulation (EU) 2017/745.
- The activities will include both the evaluation of technical documentation and audits of the Quality Management System (QMS), including audits according to EN ISO 13485.
- This opportunity is exclusively reserved for candidates residing in Italy. Work location: Rho/Emilia Romagna Requirements Product Reviewer / Final Reviewer
- Degree in engineering or chemical sciences or pharmacy
- Minimum 4 years of work experience with a medical device manufacturer, of which at least 2 years as a product reviewer with Notified Bodies
- Solid knowledge of Regulation (EU) 2017/745 and Directive 93/42/CEE (MDD)
- Solid knowledge of the main horizontal harmonized standards, including but not limited to ISO 14971, ISO 10993 series, EN 62366 English language skills
- Preferable knowledge of MDR codes: MDA 0201, 0202, 0303, 0306, 0307, 0311, 0312, MDN 1102, 1201, 1202, 1203 Auditor
Additional details
- This opportunity is exclusively reserved for candidates residing in Italy. Work location: Rho/Emilia Romagna Product Reviewer / Final Reviewer
- Solid knowledge of the main horizontal harmonized standards, including but not limited to ISO 14971, ISO 10993 series, EN 62366 English language skills
- Preferable knowledge of MDR codes: MDA 0201, 0202, 0303, 0306, 0307, 0311, 0312, MDN 1102, 1201, 1202, 1203
- Solid knowledge of the main horizontal harmonized standards, including but not limited to ISO 13485, ISO 14971
- Contact If interested, send your Curriculum Vitae to [email protected]
Notes and original content
- This opportunity is exclusively reserved for candidates residing in Italy.
- Work location: Rho/Emilia Romagna
- Requirements
- Product Reviewer / Final Reviewer
- Solid knowledge of the main horizontal harmonized standards, including but not limited to ISO 14971, ISO 10993 series, EN 62366
- English language skills
Questions about this listing
What salary does MTIC Group offer for this role?
MTIC Group lists CHF 58'000 - 78'000 gross per year for this position in Lugano Paradiso. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does MTIC Group offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with MTIC Group during the application process, since these details can vary by role even within the same contract category.
Do I need the G permit to apply for this role in Ticino as an Italian cross-border worker?
Yes, if you are resident in Italy within the 20 km border zone. The Swiss employer files the G-permit application at the Ticino cantonal migration office after the contract is signed — first issuance takes 2-6 weeks, then automatic yearly renewal for as long as the employment continues. Weekly return to your Italian home is required to keep the status.
How do I apply for this position at MTIC Group?
Use the "Apply now" button on this page — it links directly to MTIC Group's original listing at spsintercertsa.mtic-group.org, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
