RoslinCT
Senior Talent Acquisition Manager at Taylor Strategy Partners a Syneos Health Company
How You Will Make an Impact: Assist with operations in a state-of-the-art cGMP facility by providing direct support to Manufacturing and GMP support activities to ensure seamless production across shifts. Perform hands-on manufacturing processes on the production floor by executing validated protocols, batch records, and SOPs to ensure safe, compliant operations. Carry out daily aseptic sampling to evaluate cell count, viability, and other key process parameters. Process clinical material using automated, single-use systems for cell selection, expansion, harvest, and washing steps. Support inventory management, material kitting, and transfers in compliance with established SOPs. Execute setup and cleaning activities for equipment and cleanrooms per defined schedules in compliance with GMP/GDP standards. Participate in engineering and GMP runs in close collaboration with MS&T and other operational teams. Adhere to cGMP regulations and SOPs while ensuring accurate and timely completion of all associated documentation. Review in-process documentation daily to verify completeness and compliance with cGMP standards. Escalate any processing or equipment issues promptly to ensure timely resolution and minimal impact on production. Perform other duties as assigned by the Supervisor or Manager to support operational readiness and execution. What You Will Bring: A highly organized work style that ensures timely execution of tasks. A mindset that ensures accurate results. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Effective problem-solving capabilities. Strong oral and written communication skills. Qualifications: 0-5 years of experience with a Bachelor's degree in biology or related scientific discipline, or an equivalent combination of experience and education Physical ability to perform routine cleanroom tasks, including gowning and standing for extended periods. Excellent skills in Microsoft Word, Excel, and commonly used Manufacturing and Quality systems Comfortable in a fast-paced and dynamic environment with minimal direction and able to adjust workload based upon changing priorities Our Commitment All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal-opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics. #J-18808-Ljbffr
How You Will Make an Impact: Assist with operations in a state-of-the-art cGMP facility by providing direct support to Manufacturing and GMP support activities to ensure seamless production across shifts. Perform hands-on manufacturing processes on the production floor by executing validated protocols, batch records, and SOPs to ensure safe, compliant operations. Carry out daily aseptic sampling to evaluate cell count, viability, and other key process parameters. Process clinical material using automated, single-use systems for cell selection, expansion, harvest, and washing steps. Support inventory management, material kitting, and transfers in compliance with established SOPs. Execute setup and cleaning activities for equipment and cleanrooms per defined schedules in compliance with GMP/GDP standards. Participate in engineering and GMP runs in close collaboration with MS&T and other operational teams. Adhere to cGMP regulations and SOPs while ensuring accurate and timely completion of all associated documentation. Review in-process documentation daily to verify completeness and compliance with cGMP standards. Escalate any processing or equipment issues promptly to ensure timely resolution and minimal impact on production. Perform other duties as assigned by the Supervisor or Manager to support operational readiness and execution. What You Will Bring: A highly organized work style that ensures timely execution of tasks. A mindset that ensures accurate results. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Effective problem-solving capabilities. Strong oral and written communication skills. Qualifications: 0-5 years of experience with a Bachelor's degree in biology or related scientific discipline, or an equivalent combination of experience and education Physical ability to perform routine cleanroom tasks, including gowning and standing for extended periods. Excellent skills in Microsoft Word, Excel, and commonly used Manufacturing and Quality systems Comfortable in a fast-paced and dynamic environment with minimal direction and able to adjust workload based upon changing priorities Our Commitment All RoslinCT employees embrace the principles of our culture and values and are deeply committed to fostering an environment where diversity and inclusion are not only valued but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. RoslinCT is proud to be an equal-opportunity employer, we seek to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other applicable legally protected characteristics. #J-18808-Ljbffr