Quality Engineer in Le Locle

veröffentlicht
Kontakt
Caroline von Rohr, Randstad JnJ Neuchâtel Campus
Jobtyp
temporär
Jetzt bewerben

job details

veröffentlicht
Ort
Le Locle, Neuenburg
Sektor
Bau
Jobtyp
temporär
Referenznummer
170355-49
Kontakt
Caroline von Rohr, Randstad JnJ Neuchâtel Campus
Telefon
032 934 80 81
Jetzt bewerben

Stellenbeschreibung

Randstad has over 55 years of experience in the area of HR Management. Under the Randstad Inhouse Services concept, Randstad becomes a full service supplier providing consultancy to international clients. For our client, a multinational company based in Le Locle and specialised in medical devices and diagnostics, we are seeking for a:


Quality Engineer (m/w) 100%


General Summary:


Provides overall quality assurance leadership in the management of select contract manufacturing sites engaged in the production of Johnson and Johnson products. Conducts audits to good manufacturing practices, international organization for standardization and any other applicable standards.


Duties & Responsibilities:



  • Provides comprehensive product team support for quality system design and audit, compliance assessment, and for support of steady state manufacturing processes.

  • Utilizes industry and process excellence standards on a moderately complex level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO).

  • Addresses or escalates product and process complaints.

  • Evaluates contract manufacturer performance metrics and conducts management reviews.

  • Conducts audits of all quality system categories to assess compliance to process excellence standards.

  • Implements comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, demonstrating continuous improvement to man.

  • Facilitates technical issues for manufacturing processes that are to be transferred to satellite facilities

Qualifikation


  • Minimum Bachelor Degree or equivalent

  • Degree in Engineering or Life Science

  • A minimum of 2 years of experience in a GMP and/or ISO regulated industry is required

  • Experience in the medical device and/or pharmaceutical industry is preferred

  • Strong communication, teamwork, and problem solving skills are required

  • Strong root cause analysis skills are required

  • Fluency in French and English is required.

Start date : immediate