Ardena Careers · 1 month ago
Senior Associate Scientist
Somerset, NJ
Contract
Onsite
Mid, Senior Level
$70K/yr - $78K/yr
2+ years expArdena is a leading Contract Development and Manufacturing Organization (CDMO) that partners with pharmaceutical companies to aid in drug development. They are seeking a Senior Associate Scientist in Quality Control to perform analytical testing of raw materials and finished products, ensuring compliance with quality standards in a GMP-regulated laboratory environment.
Pharmaceuticals
Responsibilities
Works 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 procedures
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
Qualification
Required
AS Chemistry/Analytical Chemistry is required
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
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
Preferred
BS Chemistry/Analytical Chemistry is preferred
2+ years related experience is preferred
Benefits
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
Company
Ardena Careers
Find your career path with Ardena At Ardena, we’re more than a global Contract Development and Manufacturing Organization (CDMO)—we’re a team of innovators, problem-solvers, and experts dedicated to advancing drug development.
501-1000 employees
Funding
Current Stage
Late StageCompany data provided by crunchbase