Metric Bio
Overview
Title:
Director of Manufacturing Science & Technology Location:
Midwest US - Onsite - relocation support is provided! Context:
Biologics DS & DP CDMO About the job ***Candidates need to be based within the US for consideration*** Responsibilities
Develop annual plans for MST-related work, supervise implementation, and ensure alignment with company strategy. Lead the MST team to provide technical support to production, ensuring smooth and compliant execution of production activities. Guide and supervise the development of production-related process technologies to improve process capability, efficiency, and compliance. Resolve technical problems encountered in production and ensure stable process operation. Promote technology transfer and scale-up, ensuring process reproducibility and robustness. Support audits and inspections, ensuring the process and related documentation comply with GMP and regulatory requirements. Establish and optimize laboratory systems, procedures, and quality standards to ensure accuracy, reliability, and compliance of experimental data. Provide leadership, training, and professional development for the MST team to continuously improve their technical ability and overall performance. Qualifications
Master’s degree or above in biotechnology, pharmaceuticals, chemical engineering, or a related field. At least 10 years of relevant work experience in the biopharmaceutical industry, including more than 5 years of team management experience. Proficient knowledge in large molecule drug development, technology transfer, process optimization, and GMP compliance. Excellent problem-solving skills, communication, and teamwork spirit. Strong leadership and talent development capabilities. Proficient English skills (written and spoken). Desired Competencies (Preferred but not mandatory)
Experience with CDMO operations is preferred. Familiar with U.S. FDA and EU regulatory requirements.
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Title:
Director of Manufacturing Science & Technology Location:
Midwest US - Onsite - relocation support is provided! Context:
Biologics DS & DP CDMO About the job ***Candidates need to be based within the US for consideration*** Responsibilities
Develop annual plans for MST-related work, supervise implementation, and ensure alignment with company strategy. Lead the MST team to provide technical support to production, ensuring smooth and compliant execution of production activities. Guide and supervise the development of production-related process technologies to improve process capability, efficiency, and compliance. Resolve technical problems encountered in production and ensure stable process operation. Promote technology transfer and scale-up, ensuring process reproducibility and robustness. Support audits and inspections, ensuring the process and related documentation comply with GMP and regulatory requirements. Establish and optimize laboratory systems, procedures, and quality standards to ensure accuracy, reliability, and compliance of experimental data. Provide leadership, training, and professional development for the MST team to continuously improve their technical ability and overall performance. Qualifications
Master’s degree or above in biotechnology, pharmaceuticals, chemical engineering, or a related field. At least 10 years of relevant work experience in the biopharmaceutical industry, including more than 5 years of team management experience. Proficient knowledge in large molecule drug development, technology transfer, process optimization, and GMP compliance. Excellent problem-solving skills, communication, and teamwork spirit. Strong leadership and talent development capabilities. Proficient English skills (written and spoken). Desired Competencies (Preferred but not mandatory)
Experience with CDMO operations is preferred. Familiar with U.S. FDA and EU regulatory requirements.
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