Empowering biotech with innovative gene synthesis solutions
GenScript Biotech Corporation, headquartered in Piscataway, New Jersey, is a leading global biotechnology company specializing in gene synthesis, peptide synthesis, and antibody development. With over 1,000 employees, GenScript serves more than 20,000 customers worldwide, including major pharmaceuti...
GenScript offers competitive salaries, equity options, generous PTO, flexible remote work policies, and comprehensive health benefits to support emplo...
GenScript fosters a research-driven culture that emphasizes innovation and collaboration, encouraging employees to contribute to groundbreaking advanc...
GenScript • Pennington, NJ
GenScript is hiring a Senior Scientist for Analytical Development to lead processes suitable for GMP manufacturing of clinical trial materials. This role requires extensive technical knowledge and a proven track record in the biotechnology field.
You are a seasoned professional with extensive technical knowledge in analytical development, ideally with a background in biotechnology. Your proven track record in developing and executing processes suitable for GMP manufacturing of clinical trial materials sets you apart. You have experience in technology transfer and are eager to lead and evolve functions within a CDMO business.
You possess strong problem-solving skills and are adept at collaborating with cross-functional teams to support a broad portfolio of projects. Your ability to communicate complex scientific concepts clearly and effectively is essential for success in this role. You are committed to advancing manufacturing capabilities and ensuring compliance with industry standards.
Experience in cell and gene therapy, vaccine development, or biologics discovery is a plus. Familiarity with regulatory requirements and quality assurance processes will enhance your candidacy. You are proactive in seeking innovative solutions and are passionate about contributing to the health of humans and nature through biotechnology.
In this role, you will report to the Senior QC Manager and take on the responsibility of developing and implementing analytical methods for various clinical trial materials. You will lead efforts in technology transfer and ensure that all processes align with GMP standards. Your expertise will be crucial in supporting the manufacturing of a wide range of products, including those related to cell and gene therapy.
You will collaborate closely with other scientists and engineers to optimize processes and troubleshoot any issues that arise during production. Your leadership will help shape the analytical development function within the organization, driving improvements and efficiencies in manufacturing capabilities.
You will also be involved in training and mentoring junior staff, fostering a culture of continuous learning and development within the team. Your contributions will directly impact the success of projects and the overall mission of GenScript to provide reliable biotech solutions.
GenScript offers a dynamic work environment where innovation and collaboration are encouraged. You will have the opportunity to work on cutting-edge projects that make a real difference in the biotechnology field. The company is committed to your professional growth and provides resources for continuous learning and development.
In addition to a competitive salary, GenScript offers a comprehensive benefits package that includes health insurance, retirement plans, and opportunities for career advancement. You will be part of a team that values diversity and inclusion, and your contributions will be recognized and rewarded.
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