ADDETTO/A CONTROLLO QUALITà - NON CONFORMITà (settore ELETTRICO)

Azienda

Aziende operante nel settore medicale

Descrizione

The position serves as the liaison between Manufacturing, Internal Engineering and
External Suppliers to ensure manufacturing is effective, efficient and responsive. This position is responsible for ensuring the successful introduction of new products and successful and efficient manufacturing of products in production. This figure will provide manufacturability input to R&D development projects, design and build fixtures, design and implement work processes, create work Instructions, seek cost reductions and support verification and validation activities as required. He/she will monitor ongoing manufacturing and work to continuously improve performance to manufacturing key performance indicators (KPIs).

MAIN ACTIVITIES:
- Develop oversee and revise manufacturing procedures (test, assembly, engineering changes, etc.) and documentation requirements
- Evaluate manufacturability of parts and assemblies, suggesting and implementing improvements
- Non-conformance investigations (NCMR/MRB) and reporting
- Support and implementation of manufacturing changes and new products
- Participating in IQ/OQ activities
- Monitor, measure and review manufacturing processes, implementing new techniques
- Research, propose and implement manufacturing processes and capital expenditures which realize cost reductions, capacity increases, quality improvements and strengthen manufacturability of new products
- Work with Purchasing and R&D to qualify new suppliers and oversee ongoing quality initiatives
- Provide technical support to manufacturing to optimize production and troubleshooting
- Assist PFMEA writing and assist in verification and validation efforts

QUALIFICATIONS:
- High School Diploma
- Possess 3 or more years of manufacturing experience, preferably in medical devices or in a similarly regulated environment with exposure to a variety of manufacturing processes and techniques
- Experience developing technical documentation including assembly instructions, test procedures, etc.
- Solid skills for performing non-conformance investigations and understanding of processes, equipment and tools, e.g. multimeter, power supply, fixtures
- Good documentation, communication and interpersonal relationship skills.
- Excellent ability to communicate ideas both orally and in writing
- Able to relate with internal and external professionals with ease and enthusiasm
- Ability to manage competing priorities in a fast paced environment

LANGUAGE SKILLS:
English: written and oral, B2 level or higher
Italian: written and oral, native level

Luogo di lavoro:

Città Metropolitana di Milano

Disponibilità:

Tipologia:

Full Time

Data pubblicazione:

21/02/2020

Codice annuncio:

500256881

Visualizzazioni annuncio:

917

Nome filiale:

MOC - MILANO

Numero di candidati ricercati:

1
NOTE LEGALI:
Manpower è una compagnia eticamente responsabile. Il servizio è gratuito. I candidati ambosessi (L.903/77 - D.Lgs. n.198/2006) sono invitati a leggere l'informativa Privacy su www.manpower.it Aut. Min. Prot. N. 1116 - SG - del 26/11/04.
Il titolare della registrazione e/o candidatura dichiara di essere a conoscenza delle sanzioni penali previste in caso di dichiarazioni mendaci o contenenti dati non più rispondenti a verità come previsto dal D.P.R. nº445 del 28.12.2000

ADDETTO/A CONTROLLO QUALITà - NON CONFORMITà (settore ELETTRICO)

Città Metropolitana di Milano
Full Time
21/02/2020
500256881
917
MOC - MILANO
1

Azienda

Aziende operante nel settore medicale

Descrizione

The position serves as the liaison between Manufacturing, Internal Engineering and
External Suppliers to ensure manufacturing is effective, efficient and responsive. This position is responsible for ensuring the successful introduction of new products and successful and efficient manufacturing of products in production. This figure will provide manufacturability input to R&D development projects, design and build fixtures, design and implement work processes, create work Instructions, seek cost reductions and support verification and validation activities as required. He/she will monitor ongoing manufacturing and work to continuously improve performance to manufacturing key performance indicators (KPIs).

MAIN ACTIVITIES:
- Develop oversee and revise manufacturing procedures (test, assembly, engineering changes, etc.) and documentation requirements
- Evaluate manufacturability of parts and assemblies, suggesting and implementing improvements
- Non-conformance investigations (NCMR/MRB) and reporting
- Support and implementation of manufacturing changes and new products
- Participating in IQ/OQ activities
- Monitor, measure and review manufacturing processes, implementing new techniques
- Research, propose and implement manufacturing processes and capital expenditures which realize cost reductions, capacity increases, quality improvements and strengthen manufacturability of new products
- Work with Purchasing and R&D to qualify new suppliers and oversee ongoing quality initiatives
- Provide technical support to manufacturing to optimize production and troubleshooting
- Assist PFMEA writing and assist in verification and validation efforts

QUALIFICATIONS:
- High School Diploma
- Possess 3 or more years of manufacturing experience, preferably in medical devices or in a similarly regulated environment with exposure to a variety of manufacturing processes and techniques
- Experience developing technical documentation including assembly instructions, test procedures, etc.
- Solid skills for performing non-conformance investigations and understanding of processes, equipment and tools, e.g. multimeter, power supply, fixtures
- Good documentation, communication and interpersonal relationship skills.
- Excellent ability to communicate ideas both orally and in writing
- Able to relate with internal and external professionals with ease and enthusiasm
- Ability to manage competing priorities in a fast paced environment

LANGUAGE SKILLS:
English: written and oral, B2 level or higher
Italian: written and oral, native level
NOTE LEGALI:
Manpower è una compagnia eticamente responsabile. Il servizio è gratuito. I candidati ambosessi (L.903/77 - D.Lgs. n.198/2006) sono invitati a leggere l'informativa Privacy su www.manpower.it Aut. Min. Prot. N. 1116 - SG - del 26/11/04.
Il titolare della registrazione e/o candidatura dichiara di essere a conoscenza delle sanzioni penali previste in caso di dichiarazioni mendaci o contenenti dati non più rispondenti a verità come previsto dal D.P.R. nº445 del 28.12.2000