Quality Assurance Senior Specialist - Aequor Technologies LLC
Thousand Oaks, CA 91320
About the Job
Fully remote
Responsibilities: Coordinate Global Incoming Quality Process Operations to support Global Process Owner lead. Interface with IQA Network, various *** sites and business partners to ensure maintain process in compliance and alignment. Complete and approve multisite procedures, deviation, change control and other quality records to support RM Network. Candidate must have strong leadership skills, communication skills, and the ability to approach issues from a strategic perspective. This includes the ability to translate strategy into challenging, actionable objectives to effectively drive your team, advocate client positions throughout the life cycle of the project and make value-based decisions.
Requirements: Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation and documentation according to company guidelines. Be self motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data. Basic project management skills. Independently understand, follow and implement instructions. Strong word processing, database and spreadsheet application skills. Strong organizational skills with the ability to manage multiple projects or assignments.
Responsibilities: Coordinate Global Incoming Quality Process Operations to support Global Process Owner lead. Interface with IQA Network, various *** sites and business partners to ensure maintain process in compliance and alignment. Complete and approve multisite procedures, deviation, change control and other quality records to support RM Network. Candidate must have strong leadership skills, communication skills, and the ability to approach issues from a strategic perspective. This includes the ability to translate strategy into challenging, actionable objectives to effectively drive your team, advocate client positions throughout the life cycle of the project and make value-based decisions.
Requirements: Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation and documentation according to company guidelines. Be self motivated, attentive to details and able to prioritize and meet deadlines. Basic statistical mathematical skills including the ability to trend data. Basic project management skills. Independently understand, follow and implement instructions. Strong word processing, database and spreadsheet application skills. Strong organizational skills with the ability to manage multiple projects or assignments.
Source : Aequor Technologies LLC
