CMC Development Manager

Job Overview

Karo Healthcare is seeking a highly skilled CMC Development Manager to join their team in Stockholm, Sweden. In this pivotal role, you will be responsible for managing Chemistry, Manufacturing, and Controls (CMC) development activities, ensuring regulatory compliance, and driving the successful progression of pharmaceutical products through their lifecycle.

Company Overview

Karo Healthcare delivers smart choices for everyday healthcare, owning and commercialising branded, original over-the-counter products and prescription medicines. Their extensive portfolio covers categories such as intimate health, skin health, digestive health, foot health, pain, cough and cold, wellness, and specialty products. Available in over 90 countries and sold through various channels, Karo Healthcare has a strong sales presence in more than 10 European countries, with the Nordic region as its core market. Headquartered in Stockholm, Sweden, the company has been owned by KKR since 2025.

Quick Details

• Salary Range: Market Competitive
• Job Type: Full-time
• Qualifications: Bachelor’s Degree
• Experience: 5 Year+

Key Responsibilities

• Manage and oversee CMC development activities for new and existing pharmaceutical products.
• Ensure all CMC aspects comply with relevant global regulatory requirements and guidelines (e.g., GMP, ICH).
• Coordinate closely with R&D, manufacturing, quality assurance, and regulatory affairs teams.
• Oversee and manage outsourced development and manufacturing activities with contract organizations.
• Develop and implement CMC strategies to support product registration and lifecycle management.
• Prepare, review, and approve CMC sections for regulatory submissions globally.

Requirements

• Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific field.
• Minimum of 5 years of proven experience in CMC development within the pharmaceutical or biotechnology industry.
• In-depth understanding of global regulatory requirements, including FDA, EMA, and ICH guidelines.
• Strong project management skills with the ability to manage multiple complex projects simultaneously.
• Excellent communication, interpersonal, and negotiation skills to collaborate effectively with internal and external stakeholders.
• Proficiency in English, both written and verbal, is essential.

Benefits

• Opportunity to work with a leading and innovative global healthcare company.
• Engage in professional development and clear career advancement pathways.
• Work in a collaborative, dynamic, and supportive international team environment.
• Receive a competitive salary and comprehensive benefits package.
• Contribute directly to the development of products that enhance everyday healthcare worldwide.
• Be part of a company driven by smart choices and continuous growth.