- Act as secondary contact for Pharmacovigilance activities, monitoring post‑marketing surveillance, adverse events, product complaints, recalls, and field safety corrective actions, while supporting investigations, deviations and CAPAs.
22 days
200+ Regulatory Affairs Jobs - October 2026 - High Salaries - Page 9
Showing 257 jobs results for
"regulatory affairs"
Senior Executive - Product Compliance
- Translate and clarify compliance requirements into actionable tasks for relevant internal teams.
27 days
Senior Manager - Regional RA-QA (m-f-d)
- Quality Governance: Own SOP lifecycle management and policy alignment with global standards. Embed risk-based compliance controls across business functions. Drive continuous improvement in quality systems and post-market surveillance.
18 days
- Manage the statutory compliance calendar and drive timely completion of financial statement filing, statistical reporting and other assigned local submissions.
30+ days
RAQA Senior Specialist, SEA
- Communicate change regulations, guidance documents and industry standards that impact business to local stakeholders and global RAQA team.
30+ days
Senior Executive - Product Compliance - Market Entry
- Strong stakeholder management and concise, outcome-oriented communication skills (able to extract actionable answers efficiently).
26 days
- Contribute as part of team to maintain APAC document management system to keep product and supplier information up to date.
26 days
Assistant Vice President – Regulatory Compliance
- Review products, marketing materials and related documentation to assess compliance with applicable regulatory and industry requirements, as well as the Company’s policies.
30+ days
- Cross-Border Compliance: Partner with Product, Compliance, and Risk teams to ensure business models and cross-border settlement flows align with local laws.
28 days
- Ability to effectively identify risks to site activations and mitigate as necessary;
30+ days
Intern, CSA
- International Cyber Policy Office
30+ days
Operations - Regulatory Submissions Specialist
- SWEC & Code Submissions: Format, package, and upload technical/general SWEC code applications across all platforms.
30+ days
- Cross-Border Compliance: Partner with Product, Compliance, and Risk teams to ensure business models and cross-border settlement flows align with local laws.
30+ days
- Act as secondary contact for Pharmacovigilance activities, monitoring post‑marketing surveillance, adverse events, product complaints, recalls, and field safety corrective actions, while supporting investigations, deviations and CAPAs.
30+ days
- Ensure that all raw materials comply with policies including allergen management and risk of cross contamination.
30+ days
Operations - Regulatory Submissions Specialist (East Malaysia - PETRONAS)
- SWEC & Code Submissions: Format, package, and upload technical/general SWEC code applications across all platforms.
30+ days
Regulatory - Quality Assurance Executive
- Assist with foreign product registration and regulatory requirements.
30+ days