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 a Senior Scientist - Project Manager.

 

WHAT YOU WILL WORK ON

YOUR ROLE

The Senior Scientist – Project Manager plays a dual role in leading scientific innovation and managing bioanalytical studies. This position combines deep expertise in method development and validation with full accountability for project execution, client communication, and regulatory compliance. The role ensures scientific excellence while coordinating cross-functional teams and maintaining operational efficiency.

YOUR KEY RESPONSIBILITIES

• Lead bioanalytical projects from initiation to completion, ensuring scientific, regulatory, and operational excellence.
• Act as Study Director (SD) or Principal Investigator (PI) for GLP-compliant studies.
• Develop, validate, and optimize analytical methods (e.g., LC-MS/MS, ELISA, and qPCR).
• Serve as primary client contact, ensuring satisfaction and repeat business.
• Contribute to business development through proposals and client meetings.
• Coordinate cross-functional teams including scientists, technicians, QA, and support functions.

YOUR PROFILE                                                                                                                             

• MSc in (Bio)analytical Chemistry, Life Sciences, Pharmacy, or related field with minimum 8 years of experience in bioanalytical method development and project management.
• PhD in (Bio)analytical Chemistry, Life Sciences, Pharmacy, or related field with minimum 5 years of experience in bioanalytical method development and project management.
• Proven leadership and client engagement skills.
• Deep understanding of method development, validation, and application of techniques such as LC-MS/MS, ELISA, and qPCR in regulated environments.
• Comprehensive knowledge of GLP, GCP, FDA, EMA, and ICH guidelines relevant to bioanalytical studies.
• Hands-on experience with laboratory instruments, data interpretation, and use of LIMS and ERP/CRM systems.
• Soft skills that align with our CARE values- Communicative, Accountable, Reliable, and Excellent.

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

✔Salary Range: $118,000.00-$135,000.00

✔ A dynamic, global 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!