Senior Quality Engineer

Kindeva Drug Delivery•Los Angeles, CA

20h•Onsite

About The Position

This is an exciting opportunity to join the Kindeva team as a Senior Quality Engineer! This role will be responsible for management and oversight of their respective products to ensure compliance with regulatory standards and customer and company specifications. The Senior Quality Engineer will be able to effectively assist in troubleshooting issues related to the manufacture of their products and drive continuous improvement to the defined processes. The role involves liaison with Value Stream Engineers, Production Managers, External Customers, Regulatory and Project Teams to provide expert advice on matters relating to the product and manufacturing processes.

Requirements

Bachelors degree or higher in a science or engineering discipline
Minimum 5 years’ experience within the pharmaceutical or medical device industry.
Ability to work independently, with little or no guidance.
Working in an operational environment
Experience with investigations, deviations, Non-conformances, CAPAs

Responsibilities

Primary Quality Contact for their products
Responsible for reviewing and approving investigations for their products and, collaborating with key stakeholders and customers to ensure investigations are closed in a timely manner.
Lead effective root cause analysis / corrective action through use of cause mapping, process mapping, fishbone diagrams, etc. Effectively identify, troubleshoot and resolve non-routine problems.
Participate in New Product Introduction (NPI) activities for their respective customer/product.
Provide direction and support to Quality Improvement programs using Six Sigma principles.
Interact with Customers, through technical interfaces and audits. Be available to discuss quality issues with Customers, in compliance with Quality Agreements and to present Kindeva position.
Participate in Inspection readiness activities and Regulatory Inspections.
Review and approval of SOPs, Protocols, Technical Reports, Deviations, CAPAs, planned deviations, change controls, customer complaints, validation and other GMP documentation.