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Posted Mar 6, 2026

[Hiring] Regulatory Affairs Manager @Clinglobal Group

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This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description This role drives regional regulatory strategy for Veterinary Medicinal Products (VMPs), ensuring compliance and supporting successful product development, approval, and lifecycle management. • Lead regional regulatory activities for Veterinary Medicinal Products (VMPs) and innovation projects. • Develop and execute effective regulatory strategies in collaboration with cross-functional teams. • Provide expert guidance on regulatory pathways and support decision-making when challenges arise. • Prepare, review, and manage high‑quality regulatory submissions, including dossiers, variations, and renewals. • Coordinate submission documentation and ensure all materials are complete, accurate, and on schedule. • Build and maintain strong relationships with regulatory authorities, customers, and internal stakeholders. • Represent the company in key meetings with regional regulatory authorities. • Monitor regulatory changes, assess their project impact, and communicate actionable insights. • Identify and mitigate regulatory risks throughout the product lifecycle. • Partner with R&D and clinical teams to integrate regulatory requirements into development and trial planning. • Support and improve internal SOPs and regulatory processes to enhance efficiency and compliance. • Mentor junior regulatory staff and provide regulatory training to internal teams. • Develop and track a regional regulatory project roadmap, managing timelines and resources effectively. • Contribute to continuous improvement initiatives within the regulatory affairs function. Qualifications • A Bachelor’s degree in life sciences, pharmacy, veterinary medicine, or a related field is required. • Advanced degrees such as a Master’s (MS, MSc), Doctorate (PhD, DVM, MD, PharmD), or equivalent professional qualifications are highly preferred. • Minimum of five years’ experience in regulatory affairs, project management, or a related field, preferably within the Animal Health, Human Pharma, or Healthcare sectors. • Strong technical writing and oral presentation skills in English. • Excellent knowledge and understanding of current industry regulations and applicable local legislation. • Experience in leading cross-functional teams is a plus. • Must be willing and able to travel locally and internationally. Requirements • This is a remote position with potential for regular travel. • Applicants must be aware that Internet Explorer is not compatible with BambooHire. • The Company complies with local and international data protection and privacy legislation. • As part of the hiring process, candidates need to willingly take part in personality and behaviour assessments. • The Company may perform criminal and/or other relevant checks on all applicants applying for this position. Benefits • Compensation: $65,000 - $80,000