Senior Engineer
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Roskilde
Job Title: Senior Engineer
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit .
Overview
Your future team is a part of the Technical Service area at the ThermoFisher Site Roskilde.
The team consist of highly skilled engineers and technicians who are responsible for conducting projects and tasks related to support so we continuously can deliver products in the right quality to our customers worldwide. The work environment in the team is characterized by being warm and informal, where close collaboration and humour is an important part.
How will you make an impact?
As a validation engineer at ThermofisherFisher Site Roskilde you will play a major role in order to support and to take validation to the next level. With your open-minded attitude combined with your large knowledge on validation you be will the "go-to" person who will impact both validation and general Q-mindset within the team as well as across the site.
What will you do?
• Act as subject matter expert within all aspects of validation
• Help securing that we are constantly compliant in regards of current regulations and guidelines related to our products (MDR/IVDR, QSR, e.g. ISO14971, ISO13485 etc.)
• Proactive develop and challenge existing validation setup and suggest new optimized workflows where relevant
• Being liaison person to Q-department, production and other relevant stakeholders to secure that
• Train and educate colleagues within validation
• Work as a validation role model and sparring and mentoring on upcoming and ongoing validations
• Develop and encourage the Q-mindset amongst colleagues and stakeholders
• Able to manage and conduct complex validation projects and tasks independently according to agreed timelines on close cooperation with stakeholders
• Stay updated inside own specialist area by active search for the latest news. Join fairs, conferences, and relevant literature.
• Participate and support the Lean program (PPI)
• Manage projects and tasks related to improve capability in manufacturing processes
How will you get here?
• +10 years of validation experience from the life science industry (preferably with manufacturing of medical devices)
• Engineering background and education will be preferred (minimum bachelor level)
• Positive track record and demonstrated experience from alike positions
• Demonstrate the value of strong culture, strategic thinking and vision.
• Communicate clearly in Danish and English, both verbal and in written.
Required:
• Minimum 5 years of validation experience (as key position within validation)
• Demonstration of results in previous jobs.
• Demonstrate high work standard.
• Bachelor or comparable education background.
• Communication in English, both verbal and in written.
Please apply via http://jobs.thermofisher.com/ by 23rd August. Please apply as soon as possible, the position will be filled as soon as suitable candidate is found. Please send in your application via our website, in English.
If you have questions about Thermo Fisher Scientific and/or the position - please contact Nina Albuquerque, Sr Recruiter Nordics, [email protected]
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit .
Overview
Your future team is a part of the Technical Service area at the ThermoFisher Site Roskilde.
The team consist of highly skilled engineers and technicians who are responsible for conducting projects and tasks related to support so we continuously can deliver products in the right quality to our customers worldwide. The work environment in the team is characterized by being warm and informal, where close collaboration and humour is an important part.
How will you make an impact?
As a validation engineer at ThermofisherFisher Site Roskilde you will play a major role in order to support and to take validation to the next level. With your open-minded attitude combined with your large knowledge on validation you be will the "go-to" person who will impact both validation and general Q-mindset within the team as well as across the site.
What will you do?
• Act as subject matter expert within all aspects of validation
• Help securing that we are constantly compliant in regards of current regulations and guidelines related to our products (MDR/IVDR, QSR, e.g. ISO14971, ISO13485 etc.)
• Proactive develop and challenge existing validation setup and suggest new optimized workflows where relevant
• Being liaison person to Q-department, production and other relevant stakeholders to secure that
• Train and educate colleagues within validation
• Work as a validation role model and sparring and mentoring on upcoming and ongoing validations
• Develop and encourage the Q-mindset amongst colleagues and stakeholders
• Able to manage and conduct complex validation projects and tasks independently according to agreed timelines on close cooperation with stakeholders
• Stay updated inside own specialist area by active search for the latest news. Join fairs, conferences, and relevant literature.
• Participate and support the Lean program (PPI)
• Manage projects and tasks related to improve capability in manufacturing processes
How will you get here?
• +10 years of validation experience from the life science industry (preferably with manufacturing of medical devices)
• Engineering background and education will be preferred (minimum bachelor level)
• Positive track record and demonstrated experience from alike positions
• Demonstrate the value of strong culture, strategic thinking and vision.
• Communicate clearly in Danish and English, both verbal and in written.
Required:
• Minimum 5 years of validation experience (as key position within validation)
• Demonstration of results in previous jobs.
• Demonstrate high work standard.
• Bachelor or comparable education background.
• Communication in English, both verbal and in written.
Please apply via http://jobs.thermofisher.com/ by 23rd August. Please apply as soon as possible, the position will be filled as soon as suitable candidate is found. Please send in your application via our website, in English.
If you have questions about Thermo Fisher Scientific and/or the position - please contact Nina Albuquerque, Sr Recruiter Nordics, [email protected]
Information og data
Denne ledige stilling har jobtypen "Projektleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Roskilde.
Jobbet er oprettet på vores service den 30.7.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Projektleder
- Roskilde
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6. november 2024 | 1 |
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3. november 2024 | 1 |
2. november 2024 | 1 |
1. november 2024 | 1 |