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Senior Area Manager- APIs
Job in
Jersey City, Hudson County, New Jersey, 07390, USA
Listed on 2026-02-15
Listing for:
Jackson Hogg
Full Time
position Listed on 2026-02-15
Job specializations:
-
Business
Business Development
Job Description & How to Apply Below
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.
Position:
Senior Area Manager
The selected candidate will be responsible for:
- Developing strong, senior-level relationships with decision-makers, technical stakeholders, and regulatory functions within strategic customer accounts
- Identifying and driving new growth opportunities by expanding product portfolios and supply volumes
- Coordinating commercial, technical, and regulatory activities to ensure excellent customer service and effective management of complex projects
- Negotiating supply contracts, framework agreements, pricing, and commercial terms to secure optimal margins
- Collaborating closely with internal functions (Quality, Regulatory Affairs, R&D, Supply Chain, Finance, Production) to ensure successful project execution and customer satisfaction
- Monitoring market trends, competitive dynamics, and regulatory developments to inform commercial strategies
- Representing the organization at strategic meetings, international trade fairs, and industry conferences
- Working closely with a team of Area Managers, fostering a collaborative, results-driven culture
- MSc in a scientific discipline (Chemistry, Chemical Technologies, Biotechnology, Pharmacy)
- or
- Degree in Economics with a strong focus on the pharmaceutical sector
- 8–10+ years of commercial experience within the API, CDMO, or pharmaceutical ingredients industry
- Proven track record managing strategic international accounts and negotiating complex commercial agreements
- Strong knowledge of GMP regulations and regulatory processes (DMF, CEP, ANDA), as well as generic and branded market dynamics
- Solid understanding of the pharmaceutical product life cycle and generic market dynamics
- Ability to interpret technical and regulatory documentation
- Proficient use of CRM systems and standard Office productivity tools
- A dynamic, fast-evolving international environment that values initiative and personal contribution
- Structured training programs to support continuous professional development
- Clear internal career paths with a strong focus on internal growth and leadership development
- 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.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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