PerkinElmer is a leader in scientific solutions focused on innovating for a healthier world. They are seeking a Validation Engineer to support project execution through technical contributions and problem-solving within the life sciences sector. The role involves executing technical tasks, ensuring compliance with regulatory requirements, and contributing to business growth through high-quality deliverables.
Identify and close individual knowledge gaps with support from other team members or leads as needed
Execute system and process validation protocols by using GxP best practices
Support necessary billables as forecasted by site dashboards on billable targets per month
Report workload or skill gaps within assigned tasks
Focus on professional development and support team collaboration under the Site Leads guidance
Share technical knowledge with peers to support project delivery
Contribute to project-level success by delivering high-quality work that supports business growth opportunities
Build meaningful internal and external relationships
Present Project Farma as a service to clients as needed
Communicate with clients in a professional manner
Ensure any client feedback or opportunities identified are being escalated properly
Maintain professional relationships with project team members and client POCs at the operational level (e.g., technicians, engineers) to facilitate task completion
Maintain 100% individual billability by completing assigned project tasks
Escalate any roadblocks on achieving billable targets to the site lead
Qualification
Required
Bachelor's Degree in Life Science, Engineering, or related discipline (OR a combination of equivalent work experience in capital project engineering, pharma cGMP facility start-up, CapEx/OpEx project management and/or comparable military experience
0-2 years in consulting and/or engineering services
Willingness to travel up to 100% or as required for client projects
Ability to execute specific technical tasks within a project, ensuring high-quality deliverables
Ability to perform CQV tasks, such as protocol development or equipment testing, under the Site Lead's guidance
Ability to report technical issues to the Site Lead and support resolution efforts
Ability to ensure tasks meet client specifications, regulatory requirements (e.g., FDA, GMP), and industry standards
Ability to identify and close individual knowledge gaps with support from other team members or leads as needed
Ability to execute system and process validation protocols by using GxP best practices
Ability to support necessary billables as forecasted by site dashboards on billable targets per month
Ability to report workload or skill gaps within assigned tasks
Ability to focus on professional development and support team collaboration under the Site Leads guidance
Ability to share technical knowledge with peers to support project delivery
Ability to contribute to project-level success by delivering high-quality work that supports business growth opportunities
Ability to build meaningful internal and external relationships
Ability to present Project Farma as a service to clients as needed
Ability to communicate with clients in a professional manner
Ability to ensure any client feedback or opportunities identified are being escalated properly
Ability to maintain professional relationships with project team members and client POCs at the operational level (e.g., technicians, engineers) to facilitate task completion
Ability to maintain 100% individual billability by completing assigned project tasks
Ability to escalate any roadblocks on achieving billable targets to the site lead
Preferred
Benefits
PerkinElmer focused on improving the health and safety of people and the environment.
