Scientist II / Senior Scientist I in Engineering – Method Development (all genders) (full-time, permanent)
AbbVie
Scientist II / Senior Scientist I in Engineering – Method Development (all genders) (full-time, permanent)
Job Description
The job that makes possibilities real in patients' lives. And yours.The job that helps you get ahead in life. Moving mountains together.Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place!Moving mountains together – as Scientist II / Senior Scientist I in Engineering – Method Development (all genders) (full-time, permanent)We are looking for an experienced Senior Scientist I, Engineering – Method Development (all genders) to join our Device and Combination Product Development to contribute to the development of exciting new drug / device combination products.Your tasks and responsibilitiesSubject Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer.Design Verification: Author verification protocols and reports. Support investigations and issue resolutions.Execute test protocols supporting exploratory and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams. Utilize Zwick Universal Test Machine (UTM) and other GMP and non-GMP test equipment used for combination product development and Design Verification.Software Tools: Utilize Electronic Lab Notebook (ELN) software and electronic DHF tools such as Polarian.Implementing process automation and digitalization initiatives to enhance efficiency and reliability in device development and manufacturing processes.Utilizing analytical modelling for key performance attributes and ensuring compliance with regulatory requirements, including FDA, EMA, and ISO standards.
Locations
- Ludwigshafen, RP
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
80,000 - 120,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Test Method Development and Validationintermediate
- Design Verification and Protocol Authoringintermediate
- Data Analysis and Cross-Functional Presentationintermediate
- Operation of Zwick Universal Test Machine (UTM) and GMP/Non-GMP Equipmentintermediate
- Electronic Lab Notebook (ELN) and DHF Tools (e.g., Polarian)intermediate
- Process Automation and Digitalizationintermediate
- Analytical Modelling and Regulatory Compliance (FDA, EMA, ISO)intermediate
Required Qualifications
- Experienced Senior Scientist I in Engineering – Method Development (experience)
- Background in device and combination product development (experience)
- Passion for improving global health care and patients' quality of life (experience)
- Ability to work in a challenging environment with opportunities for skill development (experience)
Responsibilities
- Serve as Subject Matter Expert (SME) for Test Method Development of delivery devices and combination products, including development, validation, and transfer
- Author verification protocols and reports for Design Verification, support investigations and issue resolutions
- Execute test protocols for exploratory and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams
- Utilize Zwick Universal Test Machine (UTM) and other GMP and non-GMP test equipment for combination product development and Design Verification
- Utilize Electronic Lab Notebook (ELN) software and electronic DHF tools such as Polarian
- Implement process automation and digitalization initiatives to enhance efficiency and reliability in device development and manufacturing processes
- Utilize analytical modelling for key performance attributes and ensure compliance with regulatory requirements, including FDA, EMA, and ISO standards
Benefits
- general: Opportunity to address unmet medical needs in collaboration with 48,000 employees worldwide and 3,000 in Germany
- general: Challenging work environment with opportunities for developing and increasing skills
- general: Contribution to improving patients' quality of life through expertise
- general: Full-time, permanent position as part of an international company
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Scientist II / Senior Scientist I in Engineering – Method Development (all genders) (full-time, permanent)
AbbVie
Scientist II / Senior Scientist I in Engineering – Method Development (all genders) (full-time, permanent)
Job Description
The job that makes possibilities real in patients' lives. And yours.The job that helps you get ahead in life. Moving mountains together.Welcome to AbbVie! As part of an international company with 48,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? Youve come to the right place!Moving mountains together – as Scientist II / Senior Scientist I in Engineering – Method Development (all genders) (full-time, permanent)We are looking for an experienced Senior Scientist I, Engineering – Method Development (all genders) to join our Device and Combination Product Development to contribute to the development of exciting new drug / device combination products.Your tasks and responsibilitiesSubject Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer.Design Verification: Author verification protocols and reports. Support investigations and issue resolutions.Execute test protocols supporting exploratory and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams. Utilize Zwick Universal Test Machine (UTM) and other GMP and non-GMP test equipment used for combination product development and Design Verification.Software Tools: Utilize Electronic Lab Notebook (ELN) software and electronic DHF tools such as Polarian.Implementing process automation and digitalization initiatives to enhance efficiency and reliability in device development and manufacturing processes.Utilizing analytical modelling for key performance attributes and ensuring compliance with regulatory requirements, including FDA, EMA, and ISO standards.
Locations
- Ludwigshafen, RP
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
80,000 - 120,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Test Method Development and Validationintermediate
- Design Verification and Protocol Authoringintermediate
- Data Analysis and Cross-Functional Presentationintermediate
- Operation of Zwick Universal Test Machine (UTM) and GMP/Non-GMP Equipmentintermediate
- Electronic Lab Notebook (ELN) and DHF Tools (e.g., Polarian)intermediate
- Process Automation and Digitalizationintermediate
- Analytical Modelling and Regulatory Compliance (FDA, EMA, ISO)intermediate
Required Qualifications
- Experienced Senior Scientist I in Engineering – Method Development (experience)
- Background in device and combination product development (experience)
- Passion for improving global health care and patients' quality of life (experience)
- Ability to work in a challenging environment with opportunities for skill development (experience)
Responsibilities
- Serve as Subject Matter Expert (SME) for Test Method Development of delivery devices and combination products, including development, validation, and transfer
- Author verification protocols and reports for Design Verification, support investigations and issue resolutions
- Execute test protocols for exploratory and verification testing, analyze data, document in lab notebooks, and present results to cross-functional teams
- Utilize Zwick Universal Test Machine (UTM) and other GMP and non-GMP test equipment for combination product development and Design Verification
- Utilize Electronic Lab Notebook (ELN) software and electronic DHF tools such as Polarian
- Implement process automation and digitalization initiatives to enhance efficiency and reliability in device development and manufacturing processes
- Utilize analytical modelling for key performance attributes and ensure compliance with regulatory requirements, including FDA, EMA, and ISO standards
Benefits
- general: Opportunity to address unmet medical needs in collaboration with 48,000 employees worldwide and 3,000 in Germany
- general: Challenging work environment with opportunities for developing and increasing skills
- general: Contribution to improving patients' quality of life through expertise
- general: Full-time, permanent position as part of an international company
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