A global pharmaceutical CDMO, recognized as a leader in the development and manufacturing of active pharmaceutical ingredients (APIs), is seeking to strengthen its Sales organization.
The company operates multiple manufacturing sites and R&D centers worldwide, integrating chemical synthesis and biological processes while adhering to the highest international standards of safety, quality, and environmental compliance.
The selected candidate will be responsible for:
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Developing strong, senior-level relationships with decision-makers, technical stakeholders, and regulatory functions within strategic customer accounts
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Identifying and driving new growth opportunities by expanding product portfolios and supply volumes
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Coordinating commercial, technical, and regulatory activities to ensure excellent customer service and effective management of complex projects
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Negotiating supply contracts, framework agreements, pricing, and commercial terms to secure optimal margins
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Collaborating closely with internal functions (Quality, Regulatory Affairs, R&D, Supply Chain, Finance, Production) to ensure successful project execution and customer satisfaction
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Monitoring market trends, competitive dynamics, and regulatory developments to inform commercial strategies
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Representing the organization at strategic meetings, international trade fairs, and industry conferences
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Working closely with a team of Area Managers, fostering a collaborative, results-driven culture
Requirements
Education
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MSc in a scientific discipline (Chemistry, Chemical Technologies, Biotechnology, Pharmacy)
or -
Degree in Economics with a strong focus on the pharmaceutical sector
Experience
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8–10+ years of commercial experience within the API, CDMO, or pharmaceutical ingredients industry
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Proven track record managing strategic international accounts and negotiating complex commercial agreements
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Strong knowledge of GMP regulations and regulatory processes (DMF, CEP, ANDA), as well as generic and branded market dynamics
Technical Skills
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Solid understanding of the pharmaceutical product life cycle and generic market dynamics
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Ability to interpret technical and regulatory documentation
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Proficient use of CRM systems and standard Office productivity tools
What’s Offered
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A dynamic, fast-evolving international environment that values initiative and personal contribution
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Structured training programs to support continuous professional development
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Clear internal career paths with a strong focus on internal growth and leadership development
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An inclusive workplace that values cultural diversity and different perspectives
The company is committed to equal employment opportunities and provides a workplace free from discrimination in accordance with applicable local laws.
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Consultant
Lexie Farrar
Lexie primarily focuses on Precision Medicine, OMICS and CGT tools within the US and Europe. Lexie joined Jackson Hogg at the beginning of May 2024 with 4 years of experience in life science recruitment. She has worked with a variety of businesses in this area ranging from early stage startups to 5000+ people global organisations; on cross-functional roles from R&D to Sales.
Managing Consultant - Science
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