
501 - 1000 employees
🏭 Manufacturing
💼 Consulting
🧬 Biotechnology
Manufacturing • Consulting • Biotechnology
Ardena Careers is a fully integrated Contract Development & Manufacturing Organization (CDMO) focused on navigating drug development and bringing molecules to the clinics. With over 500 professionals across six sites in Belgium, The Netherlands, Sweden, Latvia, and Spain, Ardena specializes in pharmaceutical development, formulation development, pilot batch manufacturing, and drug quality control. They offer opportunities for career growth in an innovative environment.
🕒 May 1
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501 - 1000 employees
🏭 Manufacturing
💼 Consulting
🧬 Biotechnology
Manufacturing • Consulting • Biotechnology
Ardena Careers is a fully integrated Contract Development & Manufacturing Organization (CDMO) focused on navigating drug development and bringing molecules to the clinics. With over 500 professionals across six sites in Belgium, The Netherlands, Sweden, Latvia, and Spain, Ardena specializes in pharmaceutical development, formulation development, pilot batch manufacturing, and drug quality control. They offer opportunities for career growth in an innovative environment.
• Hold full P&L accountability for the Bioanalytical Business Unit, including revenue performance, cost control, margin optimization, and financial outcomes • Lead annual budgeting, quarterly forecasting, and long‑range planning, including OPEX and CAPEX • Develop and execute business strategies that drive sustainable growth, profitability, and return on investment • Establish and monitor financial, operational, and commercial KPIs, translating data into decisive action • Build, launch, and scale the U.S. bioanalytical laboratory with strong scientific capability and operational excellence • Ensure high‑quality delivery of GLP and non‑GLP bioanalytical studies • Provide visible, inspiring leadership; coach, develop, and empower a high‑performing leadership team • Serve as the senior scientific and business representative for prospective and existing clients
• Master’s or PhD in (Bio)Chemistry, Analytical Sciences, or a related discipline • 8+ years of experience in the pharmaceutical, biotech, or CDMO environment, including senior leadership roles • Proven experience leading teams, managing business performance, and driving growth • Strong knowledge of GLP requirements and bioanalytical development from preclinical through Phase I–III • Exceptional communication, influence, and stakeholder management skills • Comfortable operating in a dynamic, fast‑growing, and evolving business environment
• Competitive compensation, including a bonus incentive plan • Flexible working hours
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