Archiviertes Projekt - Package Engineer
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Projektbeschreibung
Exciting Opportunity to join a big Medical Device client in Switzerland
Job Title: Package Engineer
OVERALL RESPONSIBILITIES:
* Perform packaging updates/changes (DCR/DCO) for processes, documentation and Bill of materials
* Execution of packaging development improvement projects
* NC & CAPA owner, investigator, and action execution
* Audit support
POSITION DUTIES & RESPONSIBILITIES:
* Plan, schedule and track project timelines using appropriate tools.
* Ownership of non-conformances within the packaging development team
* Initiate process improvements based on quality events and departmental strategy
* Audit support
* Additional duties as assigned.
* Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.
PROFESSIONAL EXPERIENCE REQUIREMENTS:
* 2 years' work experience in a regulated industry preferred
* Experience in an Medical Device or Pharmaceutical regulated environment preferred
* Quality management system experience (NC, CAPA & Audit)
* SOP & work instruction authoring experience preferred
* Experience in project execution
* Experience in improvement projects desirable
* Proven exceptional written and oral presentation skills
EDUCATIONAL REQUIREMENTS:
* Bachelor's degree in business, information systems or related discipline, or equivalent and extensive related project experience.
* Certificates in Program/Project Management will enhance candidacy but are not an requirement
OTHER REQUIREMENTS:
* Strong knowledge and skills in MS Office
* Knowledge and skills in PLM system, ex. Windchill, Agile, Adaptive, SAP will enhance candidacy
* Must be highly organized, inivative, consciences, creative, articulate, and analytical
* Strong interpersonal and diplomatic skills
* Ability to multi-task independently with minimal supervision
* German language is a plus! & Fluent English
Job Title: Package Engineer
OVERALL RESPONSIBILITIES:
* Perform packaging updates/changes (DCR/DCO) for processes, documentation and Bill of materials
* Execution of packaging development improvement projects
* NC & CAPA owner, investigator, and action execution
* Audit support
POSITION DUTIES & RESPONSIBILITIES:
* Plan, schedule and track project timelines using appropriate tools.
* Ownership of non-conformances within the packaging development team
* Initiate process improvements based on quality events and departmental strategy
* Audit support
* Additional duties as assigned.
* Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.
PROFESSIONAL EXPERIENCE REQUIREMENTS:
* 2 years' work experience in a regulated industry preferred
* Experience in an Medical Device or Pharmaceutical regulated environment preferred
* Quality management system experience (NC, CAPA & Audit)
* SOP & work instruction authoring experience preferred
* Experience in project execution
* Experience in improvement projects desirable
* Proven exceptional written and oral presentation skills
EDUCATIONAL REQUIREMENTS:
* Bachelor's degree in business, information systems or related discipline, or equivalent and extensive related project experience.
* Certificates in Program/Project Management will enhance candidacy but are not an requirement
OTHER REQUIREMENTS:
* Strong knowledge and skills in MS Office
* Knowledge and skills in PLM system, ex. Windchill, Agile, Adaptive, SAP will enhance candidacy
* Must be highly organized, inivative, consciences, creative, articulate, and analytical
* Strong interpersonal and diplomatic skills
* Ability to multi-task independently with minimal supervision
* German language is a plus! & Fluent English
Kontaktdaten
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