Regulatory Affairs Manager at AMGOMED | GlassEver Jobs

Regulatory Affairs Manager at AMGOMED | GlassEver Jobs

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Jobs / Regulatory Affairs Manager

Regulatory Affairs Manager

Islamabad Oct 07, 2026 FULLTIME

Job Description

Company Description AMGOMED is a healthcare-focused organization committed to delivering safe, effective, and high-quality medical products and services. The company emphasizes strong regulatory practices and robust quality systems to ensure compliance with local and international standards. AMGOMED values collaboration, professional development, and a culture of continuous improvement. Team members are encouraged to contribute ideas that enhance patient safety, product reliability, and operational efficiency.

Role Description The Regulatory Affairs Manager is a full-time, on-site role based in Islamabad. This role is responsible for overseeing regulatory strategy, ensuring that AMGOMED’s products and processes comply with applicable regulatory requirements, and maintaining up-to-date documentation. Day-to-day tasks include preparing, reviewing, and submitting regulatory dossiers, coordinating with internal teams on regulatory timelines, and monitoring changes in local and international regulations. The manager will collaborate closely with quality assurance, manufacturing, and R&D to support product registrations, renewals, and audits, and will provide guidance and training on regulatory standards to relevant stakeholders.

Qualifications • Candidates should possess strong expertise in Regulatory Affairs and Regulatory Requirements relevant to healthcare and medical products. • Candidates should possess skills in Regulatory Compliance and Regulatory Submissions, including preparation, review, and lifecycle management of regulatory dossiers. • Candidates should possess experience with Quality Systems, including implementation, maintenance, and continuous improvement of compliant processes. • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biomedical Engineering, or a related field. • Proven experience in a regulatory affairs role within healthcare, pharmaceuticals, medical devices, or a similar regulated industry. • Strong analytical, documentation, and organizational skills, with attention to detail and the ability to meet deadlines. • Effective communication and collaboration skills for working with cross-functional teams and regulatory authorities. • Ability to work on-site in Islamabad and adapt to evolving regulatory landscapes and business needs.