Senior Associate Scientist

Introduction to ArdenaAs 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 Associate Scientist, Quality Control.WHAT YOU WILL WORK ONYOUR ROLEThe Senior Associate Scientist, QC performs analytical testing of raw materials, in-process samples, finished products, and stability samples to ensure compliance with established quality standards. This role applies standard analytical techniques, evaluates and documents results, and supports investigations and technical documentation in a GMP-regulated laboratory environment. The position requires strong scientific judgment, attention to data integrity, and effective collaboration to support timely QC operations and product development.YOUR KEY RESPONSIBILITIESWorks on problems of moderate scope where analysis requires evaluation and exercises judgement within defined practices. With minimal supervision completes and performs analytical activities 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.Assists in investigations, and writing technical documents, such as protocols, test methods, test reports, certificate of analysis and operating proceduresKeeps 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 AS Chemistry/Analytical Chemistry is required.BS Chemistry/Analytical Chemistry is preferred.2+ years related experience is preferred.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 formAbility to work effectively under pressure to meet deadlinesMathematical 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.                                                                                                                                                              WHAT WE OFFERAt 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 impactSalary range for this role is $70,000 - $78,000.HOW TO APPLYReady to start your career path with Ardena? Click the application button and join us in shaping the future of drug development