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Apollopros is seeking a Research Associate III - Assay Development for an onsite contract role in the United States. You will design and execute experiments, analyze data, maintain compliant documentation, and collaborate with cross-functional teams to advance diagnostic assay development and regulated processes.
The role emphasizes GLP/GMP-compliant documentation, data reporting, and potential collaboration on process improvements and patentable ideas within a regulated laboratory environment.
Research Associate III - Assay Development (Contract) Work Arrangement: Onsite Experience Level: Research Associate III Experience Required: 4-6 Years of Relevant Post-College Experience Advance Innovative Assay Development and Laboratory Research We are seeking a talented Research Associate III - Assay Development to join a collaborative scientific team supporting research, development, and manufacturing initiatives in a regulated laboratory environment. This is an excellent opportunity for a hands-on scientist who enjoys experimental design, data analysis, problem-solving, and contributing to the development of advanced diagnostic and laboratory technologies. In this role, you will help drive assay development projects by designing and executing experiments, analyzing results, maintaining compliant documentation, and collaborating with cross-functional teams to deliver high-quality scientific outcomes.
Research & Experimental Execution Design, execute, and analyze experimental protocols with minimal supervision. Conduct laboratory research and development activities that support assay development and manufacturing projects. Make scientific observations, interpret results, and apply technical expertise to project strategies. Select and implement appropriate methods and techniques to solve complex technical challenges. Data Analysis & Scientific Reporting Prepare technical reports, study summaries, protocols, presentations, and quantitative analyses. Clearly communicate scientific findings and project updates to team members and stakeholders. Maintain accurate, complete, and well-organized laboratory records and documentation. Ensure compliance with applicable quality and regulatory standards, including: Good Laboratory Practices (GLP) Good Manufacturing Practices (GMP) Design Control requirements Problem Solving & Continuous Improvement Troubleshoot experimental, process, or technical issues and implement corrective actions. Contribute innovative ideas and recommendations to improve laboratory processes and workflows. Support the identification and development of potentially patentable innovations. Participate in project planning and provide scientific input to support team goals. Team Collaboration & Leadership Work effectively within a cross-functional and collaborative laboratory environment. Train and mentor colleagues on laboratory practices, processes, and procedures. Help ensure quality standards through adherence to the "Quality First Time" principle. Foster a culture of continuous learning, accountability, and scientific excellence.
Education & Experience Bachelor's degree in Life Sciences or a related scientific discipline with 4-6 years of relevant post-college experience, OR Master's degree in Life Sciences or a related field with 1-2 years of relevant post-college experience.
Hands-on proficiency with common wet-laboratory techniques, including: Pipetting Weighing and balance operation Stir plate usage General laboratory experimentation Ability to review and interpret scientific literature to support research activities. Strong proficiency with Microsoft Office applications, including: Word Excel PowerPoint Demonstrated ability to analyze complex scientific data and generate clear, evidence-based technical reports.
Excellent technical writing and documentation abilities. Strong communication and presentation skills. Meticulous attention to detail and commitment to data integrity. Proven ability to learn quickly, accept feedback, and adapt in a dynamic environment. Collaborative mindset with strong interpersonal and teamwork skills.
Candidates with experience in the following areas are highly desirable: Signals Electronic Laboratory Notebook (eLN) Minitab statistical software GLP-compliant laboratory environments Design Control processes Medical device development or regulated product development SAFe (Scaled Agile Framework) methodologies Agile planning, reporting, and project management practices.
This contract role offers the opportunity to contribute to meaningful scientific innovation while gaining experience in assay development, regulated laboratory operations, and cross-functional product development. You'll work alongside experienced scientists and researchers in a collaborative environment focused on advancing high-impact technologies and delivering quality scientific results.