Key Account Manager

Job not on LinkedIn

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

💰 Account Manager

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Viatris

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2020

🏥 Healthcare

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Healthcare • Pharmaceuticals • Healthcare Insurance

Viatris is a global healthcare company committed to improving access to high-quality medicines for patients worldwide. They offer a diverse range of products including brands and generics, and focus on various therapeutic areas that address both noncommunicable and infectious diseases. Viatris operates with a goal of providing reliable medication supply, ensuring that patients receive the treatments they need when and where they need them. The company is dedicated to healthcare empowerment, facilitating healthier living through various stages of life, supported by their global healthcare gateway. Their operations are grounded in a strong commitment to sustainability, corporate governance, and regulatory compliance across different geographies.

📋 Description

• Independently prepare regulatory assessments and contribute to global regulatory strategies across the drug development and manufacturing lifecycle, supporting the Upjohn product portfolio • Ensure regulatory conformance and consistency globally, in compliance with external regulatory requirements and internal quality procedures • Develop robust regulatory strategies to mitigate risk • Prepare and deliver high-quality CMC regulatory submissions and submission management plans for global regulatory agencies • Serve as CMC representative on core project teams, assessing regulatory risks and shaping global regulatory strategies • Manage regulatory issues and track regulatory commitments and timelines across projects, products and markets • Author and/or coordinate CMC activities for new registrations, post-approval changes, renewals, annual reports and line extensions, including responses to Agency queries • Act as a technical and scientific resource, providing guidance on complex projects and mentoring colleagues • Build effective relationships with local and global partners across R&D, Quality, and Regulatory teams

🎯 Requirements

• Bachelor's degree (or equivalent); a Master's degree is preferred, and a combination of education and experience will be considered • Significant pharmaceutical experience (Quality, Technical Services or R&D), including a number of years of pharmaceutical regulatory experience • Hands-on CMC authoring experience (initial registrations or post-approval variations) • Solid understanding of development and commercial activities and cGMPs required to assess the technical, scientific and regulatory merits of CMC information • Advanced written and oral communication skills • Prior experience managing projects • Computer literacy in Microsoft Office Suite and Documentum-based applications • Ability to work autonomously with minimal supervision, exercising independent judgment on complex, non-standardized problems

🏖️ Benefits

• Excellent career progression opportunities • Work-life balance initiatives • Bonus scheme • Health insurance • Pension • Competitive salaries • Inclusive environment