Sr Quality Specialist, Systems

Sr Quality Specialist, Systems page is loaded## Sr Quality Specialist, Systemslocations : Rochester, Michigantime type : Full timeposted on : Posted Todayjob requisition id : R002562We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. Job Description Summary The Senior Quality Specialist, Systems monitors, tracks, and trends Non-Conformances, CAPA, complaints and other Quality Systems, assesses the risk level associated with Non-Conformances and escalates the issue to management. Gathers, analyzes, reports, and presents metrics to the Quality Systems and Technology Department for the corporate Quality Index. Reviews or approves the Site Quality Review for complaint investigations and monitors complaints to ensure that potential field alerts are investigated within 72 hours. May attend meetings in place of the Manager Quality Systems and determines priorities and makes appropriate decisions. The job requires coordination with different departments within the respective site as well as the Quality Systems and Technology department to ensure compliance to current Standard Operating Procedures for the Quality Systems defined within the corporation and government regulations. All incumbents are responsible for following applicable Division & Company policies and procedures. Job Description Scope of AuthorityManages the Quality Systems at his / or her site as well as metrics, but may also assist other sites with metrics on an as needed basisKey Accountabilities - Continuous Improvement

• Monitors, tracks, and trends CAPA and complaints, tracks due dates, analyzes data, prepares reports, and presents findingsCompliance
• Assesses risk level associated with NCRs, notifies Planning / Scheduling, and escalates to management
• Reviews or approves Site Quality Reviews of complaint investigations and monitors complaints to ensure that potential field alerts are investigated within 72 hours
• Attends meetings as requested in place of the Manager Quality Systems and determines priorities and makes appropriate decisions
• Initiates communication due dates for Quality Systems (NCRs, CAPA, Complaints, etc.) to ensure they are completed on time
• Reviews current Quality Systems, works with cross functional teams and recommends improvementsManagement Review
• Coordinates and prepares metrics and materials for Quality Council and Management ReviewContinuous Improvement
• Performs and evaluates CAPA effectiveness checksQualificationsEducation & Experience Minimal acceptable level of education, work experience and certifications required for the job
• BA / BS preferably in life sciences plus a minimum of 6+ years' experience in the pharmaceutical industry OR
• MS +4 years' relevant experience in pharmaceutical industryKnowledge
• Strong knowledge of all current state, federal and local standards and regulations, e.g., cGMP, OSHA, and DEA
• Strong knowledge of 21-CFR-210, 21-CFR-211 and ICH Guidelines
• Technical and quality background related to pharmaceuticalsSkills&Abilities
• Strong communication skills
• Strong focus on quality and proven ability to apply a high degree of integrity
• Customer / Stakeholder focused (understand business plans and operating environment)
• Technical Writing ability
• Clear problem-solving and decision-making skillPhysical Requirements
• Walk across plant / warehouse Disclaimer : The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required. EEO Statement : We firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.locations : Rochester, Michigantime type : Full timeposted on : Posted 20 Days AgoBe the change you wish to see. Come join us! We want the best and brightest people at Endo to help us achieve our mission to develop life-enhancing products through focused execution. Our 3,000+ global team members are united by the important role that we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward.

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