Telma Rodrigues

Quality and Compliance professional with 6+ years of experience owning quality management systems, driving non-conformance and CAPA resolution, and leading root cause analysis across regulated environments.

Background spans pharmaceutical analytical quality (GMP/GLP, ICH Q2(R2), ALCOA+ data integrity) and cross-functional compliance governance, policy and audit support.

Six Sigma Green

Belt certified, with a track record of building SOP frameworks recognised internally with a "SOP Pioneer" award. Seeking to bring proven QMS ownership and audit-readiness discipline to a regulated manufacturing and engineering environment.

Compliance & Trust and Safety Specialist - G2 - Bangalore, India

(2022-01 - 2026-01)

• Owned escalations and enforcement processes across a high-volume compliance operation, driving investigation, root cause analysis and resolution of policy violations and process breakdowns.
• Led fraud investigation and data analysis workstreams, identifying systemic risk patterns and recommending corrective and preventive actions to cross-functional stakeholders.
• Authored and governed SOPs across the compliance function, recognised internally with a "SOP Pioneer" award for improving process consistency and audit readiness.
• Partnered with policy, legal and cross-functional teams to translate regulatory and platform policy requirements into operational compliance processes.
• Used Looker, Metabase, Snowflake, SQL and Power BI to build reporting for compliance governance, trend analysis and stakeholder decision-making.

Quality Control / Quality Assurance Analyst - Cipla - India

(2019-01 - 2022-01)

• Executed and reviewed analytical testing (HPLC, GC-MS) against GMP and regulatory specifications, ensuring product quality and data integrity in a regulated pharmaceutical environment.
• Managed deviation investigations, root cause analysis and CAPA implementation, closing non-conformances within defined quality timelines.
• Supported change control processes and contributed to internal audit and inspection readiness activities.
• Maintained ALCOA+ data integrity standards across laboratory documentation and eQMS records.

Analytical Chemist - Syngene International - Bangalore, India

• Performed analytical method validation and testing (HPLC, LC-MS, GC-MS) in line with ICH Q2(R2) and GLP requirements.
• Investigated out-of-specification and out-of-trend results, driving root cause analysis and corrective actions in partnership with QA.
• Maintained laboratory quality documentation and supported audit and inspection preparedness.

MSc - Analytical Chemistry

BSc - Biological Chemistry