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Company Description GHPL LIMITED is a medical practice company headquartered in Oldbury, West Midlands, United Kingdom. The organization is focused on delivering healthcare services and supporting medical practice operations. GHPL LIMITED works within regulated healthcare environments, offering opportunities for professionals to engage with medical standards and compliance. Team members benefit from exposure to diverse healthcare processes and structured regulatory frameworks, supporting professional growth and development.
Role Description This is a full-time, on-site Regulatory Affairs Specialist role based in Pondicherry and Baddi The Regulatory Affairs Specialist will prepare, review, and maintain regulatory documentation to support product approvals and ongoing compliance. The role involves interpreting and applying regulatory requirements, monitoring changes in relevant regulations, and ensuring that company policies and procedures remain aligned with current standards. The Specialist will coordinate regulatory submissions to authorities, collaborate with cross-functional teams (such as quality assurance, operations, and clinical staff), and respond to regulatory queries or audits. Day-to-day tasks also include maintaining organized records, supporting internal training on regulatory topics, and contributing to continuous improvement of regulatory processes.
Qualifications
- Candidates should possess skills in Regulatory Documentation and Regulatory Submissions, including drafting, compiling, and tracking regulatory files.
- Candidates should possess skills in Regulatory Compliance and Regulatory Requirements, with the ability to interpret and implement relevant healthcare and medical practice regulations.
- Candidates should possess skills in Regulatory Affairs, including coordination with regulatory bodies and internal stakeholders.
- Strong attention to detail, analytical thinking, and ability to manage multiple projects and deadlines.
- Effective written and verbal communication skills for interaction with authorities and internal teams.
- Experience in healthcare, pharmaceuticals, or medical devices is preferred.
- Bachelor’s degree in life sciences, pharmacy, healthcare management, or a related field; advanced qualifications in regulatory affairs are an advantage.
- Ability to work on-site in Pune City and collaborate in a structured, team-oriented environment.
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