Sr Associate Software Engineer – Regulatory Structured Submission
Amgen
Sr Associate Software Engineer – Regulatory Structured Submission
Job Description
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
What you will do
- Work on a GxP platform supporting the automation of regulatory content
- Automate repetitive tasks using VBA, including creating macros to streamline processes and improve efficiency
- Design user-friendly interfaces within MS Office applications, including creating forms, buttons, and other interactive elements
- Implement robust error handling and debugging techniques to ensure code reliability and maintainability
- Document code and processes clearly, ensuring that others can understand and maintain the codebase
- Review and analyze existing VBA code to understand its structure and functionality
- Customize and enhance existing code to meet new requirements, including adding new features and modifying existing ones
- Test and validate changes to ensure they meet the specified requirements and do not introduce new issues
- Work collaboratively with stakeholders, including regulatory experts, to gather requirements and ensure that changes align with regulatory standards
- Provide expert technical support in validation to optimize quality, efficiency, and cost for developing, troubleshooting, and improving new and existing applications and platforms
What we expect of you
- Master's degree / Bachelor's degree and 5 to 9 years of relevant experience
- Good to have 4-5 years of experience in the Pharmaceutical Industry
Must-Have Skills
- Experienced in VBA Development
- Appian programming
- MS Office Macros and MS Office automation
- Experience of engaging with Business stakeholders for gathering requirements, demonstrating the capabilities developed and taking feedback for continual improvement
- Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technology
- Experience with Agile software development methodologies (Scrum)
- Experience in writing requirements for development of a modern web application
- Proficiency in automation tools, data systems, and validation software
- Demonstrated expertise in a scientific domain area and related technology needs
- Understanding of scientific software systems strategy, governance, and infrastructure
- Familiarity with low-code, no-code test automation software
- Technical thought leadership
- Able to communicate technical or complex subject matters in business terms
- Knowledge of DevOps, Continuous Integration, and Continuous Delivery methodology
- SAFe for Teams certification (preferred)
- Able to work under minimal supervision
- Skilled in providing oversight and mentoring team members
- Demonstrated ability in effectively delegating work
- Excellent analytical and gap/fit assessment skills
- Strong verbal and written communication skills
- Ability to work effectively with global, virtual teams
- High degree of initiative and self-motivation
- Ability to manage multiple priorities successfully
- Team-oriented, with a focus on achieving team goals
- Strong presentation and public speaking skills
Good-to-Have Skills
- Good communication skills and the ability to work with senior leadership with confidence and clarity
What you can expect of us
- Competitive benefits
- Collaborative culture
- Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
Compensation
4-5
Locations
- Hyderabad, India
Salary
Salary not disclosed
Estimated Salary Rangehigh confidence
20,000 - 35,000 USD / yearly
Source: xAI estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Experienced in VBA Developmentintermediate
- Appian programmingintermediate
- MS Office Macros and MS Office automationintermediate
- Experience of engaging with Business stakeholders for gathering requirements, demonstrating the capabilities developed and taking feedback for continual improvementintermediate
- Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technologyintermediate
- Experience with Agile software development methodologies (Scrum)intermediate
- Good communication skills and the ability to work with senior leadership with confidence and clarityintermediate
- Experience in writing requirements for development of a modern web applicationintermediate
- Proficiency in automation tools, data systems, and validation softwareintermediate
- Demonstrated expertise in a scientific domain area and related technology needsintermediate
- Understanding of scientific software systems strategy, governance, and infrastructureintermediate
- Familiarity with low-code, no-code test automation softwareintermediate
- Technical thought leadershipintermediate
- Able to communicate technical or complex subject matters in business termsintermediate
- Knowledge of DevOps, Continuous Integration, and Continuous Delivery methodologyintermediate
- SAFe for Teams certification (preferred)intermediate
- Able to work under minimal supervisionintermediate
- Skilled in providing oversight and mentoring team membersintermediate
- Demonstrated ability in effectively delegating workintermediate
- Excellent analytical and gap/fit assessment skillsintermediate
- Strong verbal and written communication skillsintermediate
- Ability to work effectively with global, virtual teamsintermediate
- High degree of initiative and self-motivationintermediate
- Ability to manage multiple priorities successfullyintermediate
- Team-oriented, with a focus on achieving team goalsintermediate
- Strong presentation and public speaking skillsintermediate
Required Qualifications
- Master's degree / Bachelor's degree and 5 to 9 years of relevant experience (experience)
- Good to have 4-5 years of experience in the Pharmaceutical Industry (experience)
Responsibilities
- Work on a GxP platform supporting the automation of regulatory content
- Automate repetitive tasks using VBA, including creating macros to streamline processes and improve efficiency
- Design user-friendly interfaces within MS Office applications, including creating forms, buttons, and other interactive elements
- Implement robust error handling and debugging techniques to ensure code reliability and maintainability
- Document code and processes clearly, ensuring that others can understand and maintain the codebase
- Review and analyze existing VBA code to understand its structure and functionality
- Customize and enhance existing code to meet new requirements, including adding new features and modifying existing ones
- Test and validate changes to ensure they meet the specified requirements and do not introduce new issues
- Work collaboratively with stakeholders, including regulatory experts, to gather requirements and ensure that changes align with regulatory standards
- Provide expert technical support in validation to optimize quality, efficiency, and cost for developing, troubleshooting, and improving new and existing applications and platforms
Benefits
- general: Competitive benefits
- general: Collaborative culture
- general: Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
Tags & Categories
Sr Associate Software Engineer – Regulatory Structured Submission
Amgen
Sr Associate Software Engineer – Regulatory Structured Submission
Job Description
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
What you will do
- Work on a GxP platform supporting the automation of regulatory content
- Automate repetitive tasks using VBA, including creating macros to streamline processes and improve efficiency
- Design user-friendly interfaces within MS Office applications, including creating forms, buttons, and other interactive elements
- Implement robust error handling and debugging techniques to ensure code reliability and maintainability
- Document code and processes clearly, ensuring that others can understand and maintain the codebase
- Review and analyze existing VBA code to understand its structure and functionality
- Customize and enhance existing code to meet new requirements, including adding new features and modifying existing ones
- Test and validate changes to ensure they meet the specified requirements and do not introduce new issues
- Work collaboratively with stakeholders, including regulatory experts, to gather requirements and ensure that changes align with regulatory standards
- Provide expert technical support in validation to optimize quality, efficiency, and cost for developing, troubleshooting, and improving new and existing applications and platforms
What we expect of you
- Master's degree / Bachelor's degree and 5 to 9 years of relevant experience
- Good to have 4-5 years of experience in the Pharmaceutical Industry
Must-Have Skills
- Experienced in VBA Development
- Appian programming
- MS Office Macros and MS Office automation
- Experience of engaging with Business stakeholders for gathering requirements, demonstrating the capabilities developed and taking feedback for continual improvement
- Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technology
- Experience with Agile software development methodologies (Scrum)
- Experience in writing requirements for development of a modern web application
- Proficiency in automation tools, data systems, and validation software
- Demonstrated expertise in a scientific domain area and related technology needs
- Understanding of scientific software systems strategy, governance, and infrastructure
- Familiarity with low-code, no-code test automation software
- Technical thought leadership
- Able to communicate technical or complex subject matters in business terms
- Knowledge of DevOps, Continuous Integration, and Continuous Delivery methodology
- SAFe for Teams certification (preferred)
- Able to work under minimal supervision
- Skilled in providing oversight and mentoring team members
- Demonstrated ability in effectively delegating work
- Excellent analytical and gap/fit assessment skills
- Strong verbal and written communication skills
- Ability to work effectively with global, virtual teams
- High degree of initiative and self-motivation
- Ability to manage multiple priorities successfully
- Team-oriented, with a focus on achieving team goals
- Strong presentation and public speaking skills
Good-to-Have Skills
- Good communication skills and the ability to work with senior leadership with confidence and clarity
What you can expect of us
- Competitive benefits
- Collaborative culture
- Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
Compensation
4-5
Locations
- Hyderabad, India
Salary
Salary not disclosed
Estimated Salary Rangehigh confidence
20,000 - 35,000 USD / yearly
Source: xAI estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Experienced in VBA Developmentintermediate
- Appian programmingintermediate
- MS Office Macros and MS Office automationintermediate
- Experience of engaging with Business stakeholders for gathering requirements, demonstrating the capabilities developed and taking feedback for continual improvementintermediate
- Excellent problem-solving skills and a passion for tackling complex challenges in drug discovery with technologyintermediate
- Experience with Agile software development methodologies (Scrum)intermediate
- Good communication skills and the ability to work with senior leadership with confidence and clarityintermediate
- Experience in writing requirements for development of a modern web applicationintermediate
- Proficiency in automation tools, data systems, and validation softwareintermediate
- Demonstrated expertise in a scientific domain area and related technology needsintermediate
- Understanding of scientific software systems strategy, governance, and infrastructureintermediate
- Familiarity with low-code, no-code test automation softwareintermediate
- Technical thought leadershipintermediate
- Able to communicate technical or complex subject matters in business termsintermediate
- Knowledge of DevOps, Continuous Integration, and Continuous Delivery methodologyintermediate
- SAFe for Teams certification (preferred)intermediate
- Able to work under minimal supervisionintermediate
- Skilled in providing oversight and mentoring team membersintermediate
- Demonstrated ability in effectively delegating workintermediate
- Excellent analytical and gap/fit assessment skillsintermediate
- Strong verbal and written communication skillsintermediate
- Ability to work effectively with global, virtual teamsintermediate
- High degree of initiative and self-motivationintermediate
- Ability to manage multiple priorities successfullyintermediate
- Team-oriented, with a focus on achieving team goalsintermediate
- Strong presentation and public speaking skillsintermediate
Required Qualifications
- Master's degree / Bachelor's degree and 5 to 9 years of relevant experience (experience)
- Good to have 4-5 years of experience in the Pharmaceutical Industry (experience)
Responsibilities
- Work on a GxP platform supporting the automation of regulatory content
- Automate repetitive tasks using VBA, including creating macros to streamline processes and improve efficiency
- Design user-friendly interfaces within MS Office applications, including creating forms, buttons, and other interactive elements
- Implement robust error handling and debugging techniques to ensure code reliability and maintainability
- Document code and processes clearly, ensuring that others can understand and maintain the codebase
- Review and analyze existing VBA code to understand its structure and functionality
- Customize and enhance existing code to meet new requirements, including adding new features and modifying existing ones
- Test and validate changes to ensure they meet the specified requirements and do not introduce new issues
- Work collaboratively with stakeholders, including regulatory experts, to gather requirements and ensure that changes align with regulatory standards
- Provide expert technical support in validation to optimize quality, efficiency, and cost for developing, troubleshooting, and improving new and existing applications and platforms
Benefits
- general: Competitive benefits
- general: Collaborative culture
- general: Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
Tags & Categories