2 Pharmaceutical Regulatory Affairs Manager jobs in whatjobs
Pharmaceutical Regulatory Affairs Manager
Posted 20 days ago
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Job Description
Our client, a leading pharmaceutical company, is actively seeking a seasoned Pharmaceutical Regulatory Affairs Manager to lead their remote regulatory strategy. This senior role is critical for ensuring compliance with global regulatory requirements for drug development, approval, and post-market surveillance. You will be responsible for developing and implementing comprehensive regulatory submission strategies, preparing and filing dossiers with health authorities worldwide, and maintaining ongoing communication with regulatory agencies. Key responsibilities include providing regulatory guidance throughout the product lifecycle, assessing regulatory risks and opportunities, and ensuring adherence to cGMP, GCP, and GLP guidelines. The ideal candidate possesses a deep understanding of pharmaceutical product development, clinical trials, and global regulatory landscapes, including FDA, EMA, and other relevant authorities. Exceptional analytical, scientific writing, and interpersonal skills are essential. You will manage and mentor a remote regulatory affairs team, fostering a collaborative and compliant work environment. This position requires meticulous attention to detail, strong project management capabilities, and the ability to navigate complex regulatory challenges effectively. If you are an experienced regulatory affairs professional seeking a challenging and impactful remote leadership role within the pharmaceutical industry, we invite you to apply. Your expertise will be vital in accelerating the availability of life-saving medications to patients worldwide.
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Pharmaceutical Regulatory Affairs Manager
Posted 4 days ago
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Job Description
Our client, a progressive pharmaceutical company, is seeking an experienced Pharmaceutical Regulatory Affairs Manager to oversee regulatory submissions and compliance. This role is crucial for ensuring that our client's products meet all required national and international regulatory standards. The ideal candidate will have a deep understanding of pharmaceutical regulations, extensive experience in preparing and submitting regulatory dossiers, and a proven ability to navigate complex regulatory landscapes. Responsibilities include liaising with health authorities, developing regulatory strategies, managing product registrations, and ensuring ongoing compliance with evolving regulations. You will work closely with R&D, manufacturing, and marketing teams to facilitate the successful launch and lifecycle management of pharmaceutical products. This position requires strong analytical, communication, and project management skills, with the ability to work effectively in a hybrid environment. The role is based with a strong connection to the operations in Garissa, Garissa, KE , but offers flexibility for remote and in-office collaboration. We are looking for a dedicated professional who is committed to ensuring patient safety and product quality through rigorous adherence to regulatory requirements. A background in pharmacy, life sciences, or a related field is essential. This is a challenging yet rewarding opportunity to contribute significantly to the pharmaceutical industry.
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