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Quality Assurance Manager
hace 1 mes
As a Quality Supervisor at TPR, you will provide leadership to the Quality Operations team, ensuring the delivery of high-quality products that meet regulatory requirements. This role requires excellent communication and problem-solving skills, as well as knowledge of quality systems and manufacturing processes.
Key Responsibilities- Lead a team of Quality Inspectors and technicians to perform quality tasks and coordinate schedules, staffing, and deliverables.
- Develop and implement quality systems and processes to ensure compliance with FDA and ISO requirements.
- Conduct regular performance evaluations, provide constructive feedback, and implement performance improvement plans as needed.
- Ensure smooth operations by coordinating workflows, resolving issues, and addressing concerns promptly.
- Prepare reports to communicate QC's production progress, accomplishments, and issues on a frequent basis.
- Bachelor's degree in a relevant field, such as Science, Engineering, or Administration.
- Minimum of 5 years of work-related experience in a FDA-regulated environment, such as Medical Devices or Pharmaceuticals.
- At least 3 years of previous experience in a medical device, biotechnology, or pharmaceutical industry.
- Excellent communication and problem-solving skills.
- Knowledge of quality systems, manufacturing processes, and regulatory requirements.
This role requires a strong understanding of quality systems and manufacturing processes, as well as excellent communication and problem-solving skills. The ideal candidate will be able to work in a fast-paced environment and prioritize multiple tasks and deadlines.
Equal Employment OpportunityTerumo is an equal employment opportunity employer and prohibits discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination, or any other terms and conditions of employment.
