Career Category
Information Systems
Job Description
ABOUT THE ROLE
Role Description:
We seek a skilled Validation Engineer to oversee and manage validation activities for data platforms and solutions. As a key contributor, you will collaborate closely with cross-functional teams to ensure that the data and analytics products follow the required validation processes, documentation, and comply with Amgen’s standard operating procedures, policies, and guidelines. Your expertise will be instrumental in ensuring quality and adherence to required standards so that the engineering teams can build and deploy products that are compliant.
Roles & Responsibilities:
- Plan, coordinate, and lead the execution of validation activities, including qualification and validation of data products and software applications.
- Develop, review, and approve validation documentation such as Validation Plans, Validation Protocols (IQ/OQ), and Validation Reports.
- Ensure validation strategies meet regulatory requirements and company standards.
- Write, review, and approve Installation Qualification (IQ), Operational Qualification (OQ), and Computer System Validation documents.
- Stay updated on relevant changes to Amgen’s SOPs and ensure validation practices are aligned with evolving standards.
- Collaborate with cross-functional teams, including quality assurance, system owners, business owners, RunOps, engineering, and platform teams to drive validation activities and meet project deadlines.
- Track the progress of validation activities and work closely with the product owner and scrum master to ensure validation activities timelines are aligned with the overall project plan.
- Ensure timely and effective completion of all validation activities in line with project objectives and schedules.
- Ensure proper documentation of validation activities, including deviations, change control, and non-conformance management.
- Identify opportunities for process improvements in validation activities.
- Stay current on new technologies, validation trends, and industry best practices to improve validation efficiencies.
- Collaborate and communicate effectively with the product teams.
Functional Skills:
Must-Have Skills:
- 2+ years of experience in validation in a GMP-regulated environment (pharmaceutical, biotech, medical devices, etc.).
- 5+ to 9 Years overall experience in Testing with 2+ years of experience in validation experience is mandatory.
- Experience leading software validation projects.
- Proficiency in developing and executing validation protocols (IQ, OQ, PQ), reports, and related documentation.
- Familiarity with computer system validation and software validation is a plus.
- Strong problem-solving and analytical skills.
- Excellent communication and teamwork skills. ABOUT THE ROLE
Role Description:
We seek a skilled Validation Engineer to oversee and manage validation activities for data platforms and solutions. As a key contributor, you will collaborate closely with cross-functional teams to ensure that the data and analytics products follow the required validation processes, documentation, and comply with Amgen’s standard operating procedures, policies, and guidelines. Your expertise will be instrumental in ensuring quality and adherence to required standards so that the engineering teams can build and deploy products that are compliant.
Roles & Responsibilities:
- Plan, coordinate, and lead the execution of validation activities, including qualification and validation of data products and software applications.
- Develop, review, and approve validation documentation such as Validation Plans, Validation Protocols (IQ/OQ), and Validation Reports.
- Ensure validation strategies meet regulatory requirements and company standards.
- Write, review, and approve Installation Qualification (IQ), Operational Qualification (OQ), and Computer System Validation documents.
- Stay updated on relevant changes to Amgen’s SOPs and ensure validation practices are aligned with evolving standards.
- Collaborate with cross-functional teams, including quality assurance, system owners, business owners, RunOps, engineering, and platform teams to drive validation activities and meet project deadlines.
- Track the progress of validation activities and work closely with the product owner and scrum master to ensure validation activities timelines are aligned with the overall project plan.
- Ensure timely and effective completion of all validation activities in line with project objectives and schedules.
- Ensure proper documentation of validation activities, including deviations, change control, and non-conformance management.
- Identify opportunities for process improvements in validation activities.
- Stay current on new technologies, validation trends, and industry best practices to improve validation efficiencies.
- Collaborate and communicate effectively with the product teams.
Functional Skills:
Must-Have Skills:
- 2+ years of experience in validation in a GMP-regulated environment (pharmaceutical, biotech, medical devices, etc.).
- 5+ to 9 Years overall experience in Testing with 2+ years of experience in validation experience is mandatory.
- Experience leading software validation projects.
- Proficiency in developing and executing validation protocols (IQ, OQ, PQ), reports, and related documentation.
- Familiarity with computer system validation and software validation is a plus.
- Strong problem-solving and analytical skills.
- Excellent communication and teamwork skills.
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