Associate Scientist

Introduction to Ardena

As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market. Our fully integrated services span drug substance and drug product development, manufacturing, nanomedicine, clinical logistics, bioanalytical services, state research, fill & finish, and CMC regulatory support.

With a rapidly growing international footprint, Ardena is home to over 750 professionals across six strategic locations—Belgium (Ghent), the Netherlands (Oss and Assen), Sweden (Södertälje), Spain (Pamplona), and Somerset, New Jersey (the US). Our open and transparent culture is built on collaboration, ownership, and innovation, guided by our We CARE values. We foster a communicative environment where mutual respect, accountability, and excellence empower our team.

We are looking for skilled and motivated professionals eager to grow their careers in an exciting and fast-paced environment. Whether you’re an experienced expert or just starting out, Ardena provides a dynamic workplace where you can contribute to meaningful drug development projects, expand your knowledge, and be part of a global team committed to making a difference. As an international organization, we help you navigate a career path that expands your possibilities beyond borders, opening doors to personal and professional growth without limits. Your potential to grow is limitless with us.

If you are ready to take on new opportunities, work alongside industry experts, and contribute to the future of medicine, Ardena is the place for you.

For the Ardena Business Unit based in Somerset (US), we are looking for an Associate Scientist.

What You Will Work On

YOUR KEY RESPONSIBILITIES

• Works on problems of moderate scope where analysis requires evaluation and exercises judgement within defined practices.
• With supervision completes and performs analytical activities efficiently (execution and documentation).
• Conducts QC activities required for the timely completion of sample analysis associated with raw material, in-process, finished product and stability test samples.
• Analytical techniques used include but are not limited; Chromatographic analysis, dissolution testing and standard wet chemistry using conventional methods of analysis, instrumentation and electronic systems including where applicable CDMS, LIMS, ELN.
• Performs other miscellaneous technical and administrative duties as required to meet company objectives.
  
  

YOUR PROFILE

• AS Chemistry/Analytical Chemistry is required, BS Chemistry/Analytical Chemistry is preferred.
• 1 years of relevant experience is preferred.
• Good understanding of scientific principles, concepts and compendial requirements.
• Proficiency in Microsoft Office; not limited to Teams, Word, Excel, PowerPoint.
• Individual maybe required to occasionally lift 0-15 pounds and will access GMP laboratory and plant and office areas. Required to read and understand written documents and will have frequent use of computer screens.
• Soft skills that align with our CARE values- Communicative, Accountable, Reliable, and Excellent.
• Fluent English is required.
  
  

What We Offer

At Ardena, we recognize that our people drive our success. We offer:

✔ A competitive salary with a tailor-made benefits package, including: medical, dental and vision benefits effective day one of employment

✔ Paid Time Off

✔ A dynamic, international work environment with career growth opportunities

✔ Access to Ardena Academy, our internal learning platform for professional development

✔ A chance to contribute to groundbreaking drug development projects that make a real impact

How To Apply

Ready to start your career path with Ardena? Click the application button and join us in shaping the future of drug development!