About this role
Job Title Operation Manager Location(s) Taiwan - BioLegend About Us
Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11,000+ colleagues from around the globe are vital to our success and the reason we’re able to push boundaries in pursuit of better human health.
Find your future at Revvity
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Ensures that the assigned departments and employees adhere to all policies, procedures and regulations governing processes, products, and employees as well as environmental, health and safety requirements • Ensure that manufacturing teams following all company policies and procedures at all times and takes immediate corrective actions when needed e.g. pipetting calibrations, safety training • Provide ongoing leadership, support and mentorship of direct reports and department team members • Develop, monitor and report key performance indicators and metrics and take countermeasures when necessary to ensure continued attainment of long-term goals and objectives • Create and enact plans and projects that support manufacturing’s performance goals, budgets and business strategy • Regularly collaborate with leaders of other manufacturing groups, quality control, quality assurance and product development team to achieve company’s goals and meet customer needs • Other projects or responsibilities as may be required. Minimum Qualifications – Education and Experience
• Bachelor’s degree in biology related field • More than 5 years of relevant biotechnology work experience • More than 3 years of leadership experience
Preferred Qualifications – Education and Experience
• PhD or Masters degree in biology related field • Working knowledge of equipment and process used in protein purification and conjugation process • More than 3 years of working knowledge of GMP and ISO13485 regulations as well as quality management system • Working knowledge of ERP systems