This job listing is no longer available for applications. The position may have been filled or the posting period has ended.
Job Description
Join TEKsystems as a Validation Specialist and play a crucial role in ensuring compliance with regulatory standards. You will develop and document validation protocols, collaborate with various teams, and support continuous improvement initiatives, all while working in a dynamic and supportive environment.
Key Responsibilities
Develop, execute, and document validation protocols for equipment and processes
Ensure compliance with FDA, GMP, and regulatory standards
Collaborate with Quality Assurance, Manufacturing, and Engineering teams
Analyze data and prepare validation reports
Participate in audits and inspections
Support continuous improvement initiatives
Required Qualifications
1+ year of GMP Validations
IQ, OQ, PQ validations experience
Bio Lab experience
Validation Engineering experience
Experience working with cold storage units
Preferred Qualifications
Six Sigma blackbelt
Qualification Engineer
Benefits & Perks
Medical, dental & visionCritical Illness, Accident, and Hospital insurance401(k) Retirement PlanLife InsuranceShort and long-term disabilityHealth Spending Account (HSA)Transportation benefitsEmployee Assistance ProgramTime Off/Leave (PTO, Vacation or Sick Leave)