Renaissance Lakewood, LLC · 10 hours ago
Validation Intern
Lakewood, NJ
Internship
Onsite
InternRenaissance 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
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
Required
Assist the Validation Department in maintaining compliance with GMP standards
Broad exposure to core validation disciplines including cleaning validation, computer system validation (CSV), and process validation
Develop practical skills in data analysis, documentation, and system management within a regulated pharmaceutical environment
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
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
Renaissance is a US-based contract development and manufacturing organization (CDMO) for pharmaceutical and biotech companies.
Founded in 1979
501-1000 employees
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 StageTotal Funding
unknown2025-10-13Acquired
Leadership Team
Robert Harrer
Vice President and CFO
Alexis Savoth
Human Resources Business Partner
Recent News
2025-10-13
2025-10-13
Institutional Investor
2025-08-19
Company data provided by crunchbase