PHARMAFull-time
Tech Compliance Analyst II
HYDERABAD (IN)HYBRIDPOSTED: 8/14/2026
PHARMAFull-time
HIRING ORGANIZATIONSYNEOS HEALTHBiopharmaceutical / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Manage and coordinate the writing and execution of validation protocols, specifications, test scripts, and change controls for software and equipment.
Ensure IT project portfolio deliverables comply with 21 CFR Part 11, GxP, and GCP regulatory standards.
Serve as subject matter expert for IT activities during client and regulatory agency audits and inspections.
Lead CAPA compliance efforts, perform periodic system validation reviews, and conduct impact assessments on GxP change management requests.
Deliver training on Computerized Systems Validation (CSV) principles and perform quality reviews on validation deliverables.
REQUIRED VERIFIED SKILLS
Computer System Validation (CSV)
21 CFR Part 11
GCP
GxP
SDLC
Change Control
CAPA
Audit Support
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
Syneos Health is a leading fully integrated biopharmaceutical solutions organization. They provide end-to-end clinical and commercial solutions designed to accelerate the development and commercialization of new therapies worldwide. The company combines clinical development, medical affairs, and commercialization expertise to help clients bring innovative treatments to patients faster.
TEAM SIZE: 25,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare Services
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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