Sr Associate Software Engineer
Amgen
Sr Associate Software Engineer
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
- Participate in technical discussions related to clinical Trial Management, Monitoring, and Engagement (CTMME) product team.
- Drive development/maintenance activities per release calendar by working with various members of the product team and business partners.
- Conduct user acceptance testing with the customer, including coordination of all feedback, resolution of issues, and acceptance of the study.
- Support requirements gathering and specification creation process for the development/maintenance work.
- Communicate potential risks and contingency plans with project management to ensure process compliance with all regulatory and Amgen procedural requirements.
- Participate and contribute to process product or standard methodologies initiatives and support developers and testers during the project lifecycle.
- Define, author, and present various architecture footprints i.e. Business, Logical, Integration, Security, Infrastructure, etc.
- Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations.
- Develop and implement unit tests, integration tests, and other testing strategies to ensure quality of the software following IS change control and GxP Validation process.
- Identify and resolve technical challenges/bugs & maintenance requests effectively.
- Work closely with multi-functional teams, including product management, design, and QA, to deliver high-quality software on time.
- Designing, developing, and maintaining software applications and solutions that meet business needs and ensuring the availability and performance of critical systems and applications.
- Supporting Veeva ClinOps vault (suite of applications).
- Working closely with product managers, designers, and other engineers to create/maintain high-quality, scalable software solutions and automating operations, monitoring system health, and responding to incidents to minimize downtime.
What we expect of you
- Masters/Bachelors degree and 5 to 9 years of experience in Computer Science
Must-Have Skills
- Proficiency in programming languages such as Python, JavaScript preferred or other programming languages.
- Strong understanding of software development methodologies, including Agile and Scrum.
- Experience with version control systems like Git.
- Solid understanding & Proficient in writing SQL queries.
- Working knowledge of clinical trial processes specifically software validation.
- Excellent communication skills - Explaining design decisions, collaborating with teams.
- Familiarity with relational databases (such as MySQL, SQL server, PostgreSQL etc.).
- Outstanding written and verbal communication skills, and ability to explain technical concepts to non-technical clients.
- Sharp learning agility, problem solving and analytical thinking.
- Experienced in implementing GxP projects.
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, change control.
- Experience with API integrations such as MuleSoft.
- Experience with ETL Tools (Informatica, Databricks).
- Knowledge in Veeva vault configuration/customization.
Good-to-Have Skills
- Good Problem-solving skills - Identifying and fixing bugs, adapting to changes.
What you can expect of us
- Competitive benefits
- Collaborative culture
- Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
- Support for professional and personal growth and well-being
Locations
- Hyderabad, India
Salary
Salary not disclosed
Estimated Salary Rangehigh confidence
25,000 - 40,000 USD / yearly
Source: xAI estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Proficiency in programming languages such as Python, JavaScript preferred or other programming languages.intermediate
- Strong understanding of software development methodologies, including Agile and Scrum.intermediate
- Experience with version control systems like Git.intermediate
- Solid understanding & Proficient in writing SQL queries.intermediate
- Working knowledge of clinical trial processes specifically software validation.intermediate
- Good Problem-solving skills - Identifying and fixing bugs, adapting to changes.intermediate
- Excellent communication skills - Explaining design decisions, collaborating with teams.intermediate
- Familiarity with relational databases (such as MySQL, SQL server, PostgreSQL etc.).intermediate
- Outstanding written and verbal communication skills, and ability to explain technical concepts to non-technical clients.intermediate
- Sharp learning agility, problem solving and analytical thinking.intermediate
- Experienced in implementing GxP projects.intermediate
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, change control.intermediate
- Experience with API integrations such as MuleSoft.intermediate
- Experience with ETL Tools (Informatica, Databricks).intermediate
- Knowledge in Veeva vault configuration/customization.intermediate
Required Qualifications
- Masters/Bachelors degree and 5 to 9 years of experience in Computer Science (experience)
Responsibilities
- Participate in technical discussions related to clinical Trial Management, Monitoring, and Engagement (CTMME) product team.
- Drive development/maintenance activities per release calendar by working with various members of the product team and business partners.
- Conduct user acceptance testing with the customer, including coordination of all feedback, resolution of issues, and acceptance of the study.
- Support requirements gathering and specification creation process for the development/maintenance work.
- Communicate potential risks and contingency plans with project management to ensure process compliance with all regulatory and Amgen procedural requirements.
- Participate and contribute to process product or standard methodologies initiatives and support developers and testers during the project lifecycle.
- Define, author, and present various architecture footprints i.e. Business, Logical, Integration, Security, Infrastructure, etc.
- Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations.
- Develop and implement unit tests, integration tests, and other testing strategies to ensure quality of the software following IS change control and GxP Validation process.
- Identify and resolve technical challenges/bugs & maintenance requests effectively.
- Work closely with multi-functional teams, including product management, design, and QA, to deliver high-quality software on time.
- Designing, developing, and maintaining software applications and solutions that meet business needs and ensuring the availability and performance of critical systems and applications.
- Supporting Veeva ClinOps vault (suite of applications).
- Working closely with product managers, designers, and other engineers to create/maintain high-quality, scalable software solutions and automating operations, monitoring system health, and responding to incidents to minimize downtime.
Benefits
- general: Competitive benefits
- general: Collaborative culture
- general: Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
- general: Support for professional and personal growth and well-being
Tags & Categories
Sr Associate Software Engineer
Amgen
Sr Associate Software Engineer
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
- Participate in technical discussions related to clinical Trial Management, Monitoring, and Engagement (CTMME) product team.
- Drive development/maintenance activities per release calendar by working with various members of the product team and business partners.
- Conduct user acceptance testing with the customer, including coordination of all feedback, resolution of issues, and acceptance of the study.
- Support requirements gathering and specification creation process for the development/maintenance work.
- Communicate potential risks and contingency plans with project management to ensure process compliance with all regulatory and Amgen procedural requirements.
- Participate and contribute to process product or standard methodologies initiatives and support developers and testers during the project lifecycle.
- Define, author, and present various architecture footprints i.e. Business, Logical, Integration, Security, Infrastructure, etc.
- Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations.
- Develop and implement unit tests, integration tests, and other testing strategies to ensure quality of the software following IS change control and GxP Validation process.
- Identify and resolve technical challenges/bugs & maintenance requests effectively.
- Work closely with multi-functional teams, including product management, design, and QA, to deliver high-quality software on time.
- Designing, developing, and maintaining software applications and solutions that meet business needs and ensuring the availability and performance of critical systems and applications.
- Supporting Veeva ClinOps vault (suite of applications).
- Working closely with product managers, designers, and other engineers to create/maintain high-quality, scalable software solutions and automating operations, monitoring system health, and responding to incidents to minimize downtime.
What we expect of you
- Masters/Bachelors degree and 5 to 9 years of experience in Computer Science
Must-Have Skills
- Proficiency in programming languages such as Python, JavaScript preferred or other programming languages.
- Strong understanding of software development methodologies, including Agile and Scrum.
- Experience with version control systems like Git.
- Solid understanding & Proficient in writing SQL queries.
- Working knowledge of clinical trial processes specifically software validation.
- Excellent communication skills - Explaining design decisions, collaborating with teams.
- Familiarity with relational databases (such as MySQL, SQL server, PostgreSQL etc.).
- Outstanding written and verbal communication skills, and ability to explain technical concepts to non-technical clients.
- Sharp learning agility, problem solving and analytical thinking.
- Experienced in implementing GxP projects.
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, change control.
- Experience with API integrations such as MuleSoft.
- Experience with ETL Tools (Informatica, Databricks).
- Knowledge in Veeva vault configuration/customization.
Good-to-Have Skills
- Good Problem-solving skills - Identifying and fixing bugs, adapting to changes.
What you can expect of us
- Competitive benefits
- Collaborative culture
- Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
- Support for professional and personal growth and well-being
Locations
- Hyderabad, India
Salary
Salary not disclosed
Estimated Salary Rangehigh confidence
25,000 - 40,000 USD / yearly
Source: xAI estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Proficiency in programming languages such as Python, JavaScript preferred or other programming languages.intermediate
- Strong understanding of software development methodologies, including Agile and Scrum.intermediate
- Experience with version control systems like Git.intermediate
- Solid understanding & Proficient in writing SQL queries.intermediate
- Working knowledge of clinical trial processes specifically software validation.intermediate
- Good Problem-solving skills - Identifying and fixing bugs, adapting to changes.intermediate
- Excellent communication skills - Explaining design decisions, collaborating with teams.intermediate
- Familiarity with relational databases (such as MySQL, SQL server, PostgreSQL etc.).intermediate
- Outstanding written and verbal communication skills, and ability to explain technical concepts to non-technical clients.intermediate
- Sharp learning agility, problem solving and analytical thinking.intermediate
- Experienced in implementing GxP projects.intermediate
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, change control.intermediate
- Experience with API integrations such as MuleSoft.intermediate
- Experience with ETL Tools (Informatica, Databricks).intermediate
- Knowledge in Veeva vault configuration/customization.intermediate
Required Qualifications
- Masters/Bachelors degree and 5 to 9 years of experience in Computer Science (experience)
Responsibilities
- Participate in technical discussions related to clinical Trial Management, Monitoring, and Engagement (CTMME) product team.
- Drive development/maintenance activities per release calendar by working with various members of the product team and business partners.
- Conduct user acceptance testing with the customer, including coordination of all feedback, resolution of issues, and acceptance of the study.
- Support requirements gathering and specification creation process for the development/maintenance work.
- Communicate potential risks and contingency plans with project management to ensure process compliance with all regulatory and Amgen procedural requirements.
- Participate and contribute to process product or standard methodologies initiatives and support developers and testers during the project lifecycle.
- Define, author, and present various architecture footprints i.e. Business, Logical, Integration, Security, Infrastructure, etc.
- Create and maintain documentation on software architecture, design, deployment, disaster recovery, and operations.
- Develop and implement unit tests, integration tests, and other testing strategies to ensure quality of the software following IS change control and GxP Validation process.
- Identify and resolve technical challenges/bugs & maintenance requests effectively.
- Work closely with multi-functional teams, including product management, design, and QA, to deliver high-quality software on time.
- Designing, developing, and maintaining software applications and solutions that meet business needs and ensuring the availability and performance of critical systems and applications.
- Supporting Veeva ClinOps vault (suite of applications).
- Working closely with product managers, designers, and other engineers to create/maintain high-quality, scalable software solutions and automating operations, monitoring system health, and responding to incidents to minimize downtime.
Benefits
- general: Competitive benefits
- general: Collaborative culture
- general: Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards
- general: Support for professional and personal growth and well-being
Tags & Categories