
Senior Technology Regulatory Compliance Analyst - Technology IT
- South Africa
- Permanent
- Full-time
- Lead compliance efforts for technology functions to ensure adherence to global regulatory standards, including FDA 21 CFR Part 11, GAMP 5, ICH GCP, and EMA guidelines.
- Develop, implement, and maintain compliance frameworks for Enterprise IT, Cloud Operations, and R&D.
- Provide expert advice on regulatory requirements during the development and deployment of software products.
- Ensure software products meet global regulatory requirements applicable to the life sciences industry.
- Plan and lead internal audits of IT systems and processes to assess compliance readiness.
- Support external audits and inspections by regulatory authorities and customers.
- Conduct risk assessments, identify potential compliance gaps, and oversee the implementation of mitigation strategies.
- Develop, review, and update policies, SOPs, and other documentation to align with regulatory requirements.
- Ensure validation and verification processes for IT systems and software are adequately documented and maintained.
- Collaborate with Enterprise IT, Cloud Operations, and R&D teams to embed compliance into system design, software development, and operations.
- Act as a liaison with external stakeholders, including auditors and regulatory bodies, to address compliance-related queries.
- Design and deliver training programs on regulatory compliance requirements for technology teams in India.
- Mentor and guide junior analysts to ensure consistent application of compliance principles.
- Drive continuous improvement initiatives to enhance compliance processes and frameworks across technology functions.
- Stay updated on emerging trends and regulatory changes impacting the life sciences and software development industries.
- Bachelor’s degree in Information Technology, Computer Science, Regulatory Affairs, or a related field.
- Advanced degree or certifications (e.g., RAC, CRCP, or equivalent) preferred.
- 5-10 years of experience in IT regulatory compliance, particularly in life sciences or software development.
- Strong experience with global regulatory frameworks, including FDA 21 CFR Part 11, GAMP 5, and ICH GCP.
- Comprehensive understanding of IT systems, cloud operations, and software development lifecycle (SDLC).
- Proven ability to manage audits and regulatory inspections with strong problem-solving skills.
- Excellent project management, communication, and leadership abilities.
- Experience in working with geographically dispersed teams and global stakeholders.
- Familiarity with Agile and DevOps methodologies.
- Experience with compliance in cloud-based environments and data security standards.
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