Manufacturing Executive (Biotechnology)

Company Description Credence Genomics (Pte) Ltd is a biotechnology company focused on developing clinical-grade, agnostic diagnostic tests using cutting-edge technologies. The organization is committed to advancing precision diagnostics that support timely and accurate clinical decision-making. Credence Genomics emphasizes high scientific rigor, quality, and regulatory compliance in all aspects of its work. Team members collaborate in an innovation-driven environment that values integrity, continuous improvement, and patient-centered outcomes.

Medisequence (Pvt) Ltd. subsidiary of Credence Genomics is a manufacturing facility located in Chennai, India..

Role Description This is a full-time, on-site Manufacturing Executive (Biotechnology) role based in Chennai, India. The Manufacturing Executive will oversee day-to-day manufacturing operations for clinical-grade diagnostic products, ensuring adherence to quality, safety, and regulatory standards. Responsibilities include planning and processing production schedules, Manufacturing the products according to the protocol, coordinating on Inventory and resources, and monitoring workflow to meet output and quality targets. The role will involve implementing manufacturing processes, troubleshooting operational issues, and supporting continuous improvement initiatives. The Manufacturing Executive will collaborate closely with quality assurance, R&D, and supply chain teams, maintain accurate production documentation, and support audits and inspections as required.

Qualifications

• Strong foundation in Manufacturing and Manufacturing Operations, with experience in a biotechnology production environment.
• Demonstrated Production Management skills, including planning, scheduling, and coordinating day-to-day manufacturing activities.
• Proficiency in Industrial Engineering concepts, such as process optimization, workflow design, and resource utilization.
• Well-developed Analytical Skills to interpret production data, identify trends, and propose evidence-based improvements.
• Master's degree in Biotechnology, Genetic Engineering, or Molecular Biology
• Familiarity with GMP, ISO standards, or other relevant quality and regulatory frameworks for clinical diagnostics or biomanufacturing.
• Strong documentation, organizational, and communication skills, with the ability to collaborate effectively in cross-functional teams.
• Proven ability to work on-site in a laboratory or manufacturing environment, with attention to safety protocols and compliance.