Validation Intern jobs in United States
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Renaissance Lakewood, LLC · 1 day ago

Validation Intern

Renaissance Lakewood, LLC is seeking a Validation Intern to assist the Validation Department in maintaining compliance with GMP standards. This internship provides broad exposure to core validation disciplines while developing practical skills in data analysis, documentation, and system management within a regulated pharmaceutical environment.

HealthcareManufacturingPharmaceuticalHealth CareMedical
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H1B Sponsor Likelynote

Responsibilities

Collect, organize, and analyze data from environmental monitoring and validation activities
Support drafting, sorting, and archival of validation documents per GDP (Good Documentation Practice) requirements
Assist in maintaining equipment and instrument inventories, traceability matrices, and document templates within the electronic quality management system (e.g., Valgenesis, TrackWise, Documentum etc.)
Review and update facility, equipment, and critical utility storyboards to ensure alignment with current configurations
Participate in execution of equipment qualification and cleaning validation protocols under supervision of senior validation staff
Provide support in developing and reviewing cleaning validation documentation, including sampling plans and acceptance criteria
Assist with computer system validation activities such as user requirement specifications, test scripts, and validation summary reports
Observe and contribute to process validation activities, including protocol preparation, data trending, and deviation evaluation
Collaborate with Engineering, Quality Control, and Manufacturing teams to support cross-functional validation projects

Qualification

GMP complianceCleaning validationComputer system validationData analysisDocumentation managementData integrityTeam collaboration

Required

Assist the Validation Department in maintaining compliance with GMP standards across equipment, facility, and computerized systems
Collect, organize, and analyze data from environmental monitoring and validation activities
Support drafting, sorting, and archival of validation documents per GDP (Good Documentation Practice) requirements
Assist in maintaining equipment and instrument inventories, traceability matrices, and document templates within the electronic quality management system (e.g., Valgenesis, TrackWise, Documentum etc.)
Review and update facility, equipment, and critical utility storyboards to ensure alignment with current configurations
Participate in execution of equipment qualification and cleaning validation protocols under supervision of senior validation staff
Provide support in developing and reviewing cleaning validation documentation, including sampling plans and acceptance criteria
Assist with computer system validation activities such as user requirement specifications, test scripts, and validation summary reports
Observe and contribute to process validation activities, including protocol preparation, data trending, and deviation evaluation
Collaborate with Engineering, Quality Control, and Manufacturing teams to support cross-functional validation projects

Company

Renaissance Lakewood, LLC

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Renaissance is a US-based contract development and manufacturing organization (CDMO) for pharmaceutical and biotech companies.

H1B Sponsorship

Renaissance Lakewood, LLC has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (5)
2024 (1)
2022 (2)
2020 (3)

Funding

Current Stage
Late Stage
Total Funding
unknown
2025-10-13Acquired

Leadership Team

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Robert Harrer
Vice President and CFO
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Alexis Savoth
Human Resources Business Partner
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Company data provided by crunchbase