QA Specialist

Amgen • New Albany, OH

1d • $104,287 - $141,095

About The Position

Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Specialist QA
What you will do
Let’s do this. Let’s change the world. In this role you will have the opportunity to be part of the continued expansion of Quality Operations at Amgen Ohio (AOH) supporting our growing state-of-the-art Final Drug Product (FDP) Plant. You will lead and direct cross functional staff as an informed Subject Matter Expert in the Quality deliverables. A key aspect of this role is to apply critical thinking skills to ensure quality and compliance to GMP regulations for operations and associated processes. Duties include oversight on daily manufacturing operations, development and approval of standard operating procedure, quality approval of deviations and final batch disposition. Responsibilities will include evaluation of compliance and quality issues, providing recommendations for improvement projects, and assuring progress of records to completion.

Requirements

• Doctorate degree
• Master’s degree and 2 years of Quality and/or Manufacturing experience
• Bachelor’s degree and 4 years of Quality and/or Manufacturing experience
• Associate’s degree and 8 years of Quality and/or Manufacturing experience
• High school diploma / GED and 10 years of Quality and/or Manufacturing experience

Nice To Haves

• Master's or Bachelor’s Degree in Science
• Educated in a science field with 5 years of experience in GMP/GCP operations or similarly regulated industry
• Affinity with digital innovation, data sciences and Quality engineering
• Experience in review/approval validation documentation
• Ability to complete tasks autonomously, providing updates to senior management, and identifying potential issues
• Ability in problem solving and experience in managing Root Cause Analysis / Deviation investigations
• Experience working with dynamic cross-functional teams and abilities in decision making
• Strong organizational skills, including ability to follow assignments through to completion
• Strong leadership capabilities and experience applying GMP requirements in an operational setting
• Ability to independently interact with various levels, drives tasks to completion, and is a self-starter.

Responsibilities

• Review and approve controlled documents, including Standard Operating Procedures, Validation Protocols, Validation Reports, Electronic Master Batch Records etc.
• Provide quality oversight for quality records including deviations/CAPAs, technical change controls and work orders assuring adherence to procedural requirements and confirming assessments and evaluations of different partners are complete and accurate
• Drive investigations and resolution of deviations, ensuring timely, thorough, and compliant outcomes
• Ensure that all activities & related documentation for facilities, equipment, materials and processes align with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and Controls.
• Own quality related Standard Operating Procedures, Work Instructions, Forms and Methods and ensure document control excellence, including timely periodic review of controlled documents
• Provide quality oversight for manufacturing and be responsible for batch disposition.
• Provide quality and compliance expertise & guidance and agrees on strategies related to process lifecycle management.
• Support and represent Quality during audits and inspections; may directly interact with regulatory agencies during on-site inspections.
• Support Lean Transformation and Operational Excellence initiatives
• Ensure production records and test results are accurate, complete, and inspection-ready
• Champion and lead continuous improvement initiatives to strengthen quality systems and operational performance
• Partner cross-functionally with Manufacturing, QC, Engineering, Supply Chain, and other stakeholders

Benefits

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed