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 ROLE

An Associate Scientist, under the guidance of other scientists, is primarily responsible for conducting laboratory experiments and analytical testing of raw materials, intermediates, finished product, and stability samples to ensure they meet established quality standards, by analyzing data and interpreting results, and communicating findings through reports for the development of new and existing products.

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.
• Keeps accurate and detailed records of experiments including results and conclusions.
• Provides written and verbal updates on projects and activities as required.
• Assists others as necessary for timely project completion.
• Maintains appropriate standards of cGMP, Health, Safety and Environmental.
• Adheres to company and site standards for data integrity and regulatory compliance.
• Perform duties in accordance with the company mission and values.
• Performs other miscellaneous technical and administrative duties as required to meet company objectives.
• Other tasks as required.
  
  

YOUR PROFILE

Education and Experience:

• AS Chemistry/Analytical Chemistry is required.
• BS Chemistry/Analytical Chemistry is preferred.
• 1 years of relevant experience is preferred.
  
  

Knowledge and Skills:

• Good understanding of scientific principles, concepts and compendial requirements.
• Proficiency in analytical techniques, instrumentation, and quality systems.
• Proficiency in Microsoft Office; not limited to Teams, Word, Excel, PowerPoint.
• Ability to interpret a variety of instructions furnished in written, oral, visual, or schedule form
• Ability to work effectively under pressure to meet deadlines
  
  

Physical Requirements:

• Mathematical and reasoning ability with verbal and written communication proficiency.
• 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.
  
  

Work Environment/Safety Conditions

• Must wear safety glasses, in addition to other specified PPE, in all designated areas.
• Must be fit-tested as per OSHA regulations, trained and capable of wearing air purifying respirator.
• Must follow any applicable site safety requirements.
• Must be trained in site hazardous material procedures.
• Must use approved fall prevention devices when performing elevated tasks.
• Must be capable of wearing safety shoes for 8 to 12 hours a day, depending on duration of the shift.
• Working conditions will be Temperature and Humidity controlled as needed for product.
• Individual’s primary work-area is located in the Laboratory and office area, where the noise level can be low to moderate.
  
  

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, 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
  
  

Salary range for this role is $65,000.00 - $72,000.00.

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!