TECHFull-time
Tech Compliance Analyst II
By Admin · Quality Assurance & Quality Control
HYDERABAD (IN)HYBRIDPOSTED: 9/11/2026
TECHFull-time
HIRING ORGANIZATIONSYNEOS HEALTHBiopharmaceutical / Healthcare Services
ROLE OVERVIEW
Join Syneos Health as a Tech Compliance Analyst II to manage software validation and compliance for global life sciences solutions.
ROLE DEFINITION & RESPONSIBILITIES
- •Manage and/or coordinate the writing and execution of validation protocols
- •Provide support for Information Technology's project portfolio
- •Coordinate assigned project deliverables with external consultants
- •Serve as subject matter expert for audits
- •Lead compliance efforts for CAPA plans
- •Perform training in computerized systems validation
Reporting Hierarchy: Reports to IT Compliance Manager • Team size: 5-10
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- 4+ Yrs of Experience, with Bachelor's Degree in Computer Science or related science field or equivalent
- Experience with 21 CFR Part 11 required
- Experience in computer systems validation/software development life cycle approaches
- Experience in working in a clinical trials environment, including a comprehensive knowledge of GCP regulations guidelines
PREFERRED QUALIFICATIONS
- •Familiarity with global regulatory frameworks
- •Experience with automated testing tools
REQUIRED VERIFIED SKILLS
21 CFR Part 11
Computer Systems Validation
GCP Regulations
SDLC
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Health insurance, PF, Paid leave
Competitive compensation aligned with mid-level compliance analyst standards in the life sciences sector.
ORGANIZATION CONTEXT & CULTURE
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success.
TEAM SIZE: 25,000+ employees
INDUSTRY: Biopharmaceutical / Healthcare Services
Culture: We are committed to building an inclusive culture where you can authentically be yourself and shape solutions that impact lives.
EXPECTED CAREER ROADMAP
Clear progression path into senior compliance lead or managerial roles within life sciences IT quality assurance.
APPLICATION ADVISORY
Highlight your specific experience with 21 CFR Part 11 and clinical trial regulations in your resume.
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.