Senior Quality Assurance Specialist
Randstad Life Sciences US - thousand oaks, CA
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A global Pharmaceutical company that harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, osteoporosis, inflammatory diseases and rare diseases.Making a positive difference in the world is at the heart of what we do. Join to make a difference!!Top 3 Must Have Skill Sets: Tableau; Smartsheet; Spotfire; Microsoft Project Management ApplicationAble to extract and assess data from multiple systems (LIMS, SAP, LMES, QMTS)Strong leadership skills and PM experienceExcellent conceptual problem-solving skills with demonstrated ability to bring structure to vaguely defined problems, pragmatically scope problem solving approach, and manage executionMust have change control, deviation, investigation process and technical writing experienceDay to Day Responsibilities: Interaction with RM NetworkProvides cross-functional initiative support and works with teams to solve business problemsResponsible for direction, management, planning, coordination and decisions to maintains multisite operational requirements and compliance.Employee Value Proposition: Career growth, opportunityJob ResponsibilitiesCoordinate Global Incoming Quality Process Operations to support Global Process Owner terface with IQA Network, various company sites and business partners to ensure maintain process in compliance and plete 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.Education & Qualifications Requirements: Bachelor's Degree in Life Sciences or related field or the equivalent combination of education andor 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.
Created: 2024-10-19