This role is a new role designed to drive in-process quality tasks in the Manufacturing area. The role is primarily Evening shift (3p-11:30p). This position will report to the 5W Site Quality Manager. This will be a 4-6-month assignment. Responsibilities · Responsible for ensuring GMP Standards, MMCC Compliance, Quality policies and procedures are adhered to. · Write, update, and maintain SOP's (Standard Operating Procedures) for the Quality Assurance Program related to Manufacturing. · Collaborate with external and internal audit processes. · Responsible for departmental non-conformances and implementation of corrective action ensuring all corrective actions are documented and outstanding actions closed in timely manner. · Participate in root cause analysis for Manufacturing quality outages. · Support training for line operators to ensure process checks are accurate. · Approve standard work for cells prior to production. · 100% execution of daily tasks, projects & objectives. · Conduct and monitor testing and inspection of materials and products to ensure finished product quality. · Identify coaching and training needs to meet quality standards. Qualifications and Skills Required: · Minimum 1 year of Manufacturing quality experience or related degree. · Worked in a GMP environment. · Self-motivated, · Coaching & development, · Analytical and data interpretation · Good Microsoft Office interface skills Preferred: • Experience in Lean Management
Curio Wellness is cultivating a better way of life. As a trusted healthcare partner providing safe, effective and reliable products, we seek to continually elevate the healthcare conversation through education and patient experiences that are truly transformative. Whether for our patients, partners or employees, we seek to inspire and affect innovative healthcare solutions.