Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Medical Device Manufacturing Engineer - IQ/OQ/PQ/CSV
Eingestellt von Sentinel IT LLP
Gesuchte Skills: Engineering, Engineer, Design, Cnc
Projektbeschreibung
Medical Device Manufacturing Engineer - IQ/OQ/PQ/CSV
Leading global Medical Devices/Life Science client require a number of Manufacturing Engineers for a major project on site in Solothurn, Switzerland.
MAIN RESPONSIBILITIES:
The role focuses on equipment installation & Validation (IQ/OQ/PQ) - Vendor connection - Work with facility and quality and R&D - Some CSV
Equipment design and development, testing of materials, preparation of specifications and operator instructions.
The activity is to be performed in a productive site for Medical Devices (plates, needles and instruments) mostly involving drilling and turning CNC machines. Experience with such machinery is highly advantageous, combined with a previous exposure to Medical Devices and/or Life Science industries.
We are preferably looking for dynamic, self-starters candidates, able to work very hands-on in strict cooperation with the production floor.
EDUCATION & EXPERIENCE REQUIREMENTS:
EXPERIENCE:
* 4-6 years of experience in manufacturing and/or engineering is required.
* Previous experience working in Medical Device or Life Science sector is required.
* Experience with either with packaging, Laser, Cleaning or CNC processes and equipment, required
* Six Sigma or Lean Sigma certification or 4 years of experience preferred.
* Experience developing and implementing robust automated manufacturing equipment, preferred.
ESSENTIAL:
* Bachelor of Science Degree from accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree (Master of Science Degree preferred).
* Demonstrates leadership qualities including confidence, transparency, integrity, innovation, passion, patience and tenacity.
* Demonstrates strong written, verbal and presentation skills.
* Demonstrates strong computer skills, such as the use of Microsoft Office, Minitab, and databases.
* Demonstrates positive interpersonal skills and professional interactions with coworkers.
* English fluent, as this is the company language, is required
* German at a good level (conversational) for day by day interactions with stakeholders is required
THE SUCCESSFUL APPLICANT WILL
* Provide direction and technical support regarding equipment design and development, testing of materials, preparation of specifications and operator instructions, process studies, investigations, root cause analysis, problem solving and report or presentation preparation.
* Support new equipment acquisition efforts including user requirement specifications, machine selection, installation, validation, employee training, and other related equipment responsibilities as required.
* Develop process validation strategy and writes and executes engineering studies and process validation protocols and summary reports (Installation Qualification, Operation Qualification, Performance Qualification, Computer Software Validation and Test Method Validation).
* Participate in and leads cross-functional teams which may include, but are not limited to Manufacturing Engineering, Production, Quality Assurance, Finance, Product Development and other sites.
* Act as a liaison to vendors with regard to contracted products, tools & fixtures, and their manufacture.
Please apply now for more details!
Leading global Medical Devices/Life Science client require a number of Manufacturing Engineers for a major project on site in Solothurn, Switzerland.
MAIN RESPONSIBILITIES:
The role focuses on equipment installation & Validation (IQ/OQ/PQ) - Vendor connection - Work with facility and quality and R&D - Some CSV
Equipment design and development, testing of materials, preparation of specifications and operator instructions.
The activity is to be performed in a productive site for Medical Devices (plates, needles and instruments) mostly involving drilling and turning CNC machines. Experience with such machinery is highly advantageous, combined with a previous exposure to Medical Devices and/or Life Science industries.
We are preferably looking for dynamic, self-starters candidates, able to work very hands-on in strict cooperation with the production floor.
EDUCATION & EXPERIENCE REQUIREMENTS:
EXPERIENCE:
* 4-6 years of experience in manufacturing and/or engineering is required.
* Previous experience working in Medical Device or Life Science sector is required.
* Experience with either with packaging, Laser, Cleaning or CNC processes and equipment, required
* Six Sigma or Lean Sigma certification or 4 years of experience preferred.
* Experience developing and implementing robust automated manufacturing equipment, preferred.
ESSENTIAL:
* Bachelor of Science Degree from accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree (Master of Science Degree preferred).
* Demonstrates leadership qualities including confidence, transparency, integrity, innovation, passion, patience and tenacity.
* Demonstrates strong written, verbal and presentation skills.
* Demonstrates strong computer skills, such as the use of Microsoft Office, Minitab, and databases.
* Demonstrates positive interpersonal skills and professional interactions with coworkers.
* English fluent, as this is the company language, is required
* German at a good level (conversational) for day by day interactions with stakeholders is required
THE SUCCESSFUL APPLICANT WILL
* Provide direction and technical support regarding equipment design and development, testing of materials, preparation of specifications and operator instructions, process studies, investigations, root cause analysis, problem solving and report or presentation preparation.
* Support new equipment acquisition efforts including user requirement specifications, machine selection, installation, validation, employee training, and other related equipment responsibilities as required.
* Develop process validation strategy and writes and executes engineering studies and process validation protocols and summary reports (Installation Qualification, Operation Qualification, Performance Qualification, Computer Software Validation and Test Method Validation).
* Participate in and leads cross-functional teams which may include, but are not limited to Manufacturing Engineering, Production, Quality Assurance, Finance, Product Development and other sites.
* Act as a liaison to vendors with regard to contracted products, tools & fixtures, and their manufacture.
Please apply now for more details!
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Ingenieurwesen/Technik