Sr Associate Manufacturing

Amgen • West Greenwich, RI

1d

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. Sr Associate Manufacturing What you will do Let’s do this. Let’s change the world. In this vital role you will report into the Senior Manager of MFG Support Investigation team and interact broadly across the site owning and facilitating Major deviation investigations. This role requires strong critical thinking, technical writing, and the ability to effectively manage projects to closure within defined timelines. Additionally, it drives technical growth while enhancing communication and facilitation capabilities across cross-functional teams.

Requirements

• High School/GED and 4 years of manufacturing or operations work experience OR Associate’s Degree and 2 years of manufacturing or operations work experience OR Bachelor’s Degree and 6 months of manufacturing or operations work experience OR Master’s Degree

Nice To Haves

• Familiarity with the deviation management systems and corrective/preventative actions
• Experience presenting in audits and inspection
• Project management skills with ability to maintain deliverables and timelines
• Excellent communication skills and sense of urgency
• Demonstrated ability to forge and maintain strong relationships

Responsibilities

• Lead major investigations record at the site – Managing meeting, sending minutes, RCA, identification of CAPA, and development of a deviation report
• Building technical aptitude through investigation events
• Purposeful presence on the floor walking down deviating events and investigating contributing factors
• Collaborating cross site and network with investigation leads for alignment and learning
• Representing audits and inspections presenting record defense
• Identifying and autonomously implementing continuous improvement opportunities and AI usage
• Supporting process owner tasks as applicable including but not limited to CAPA/EV owner, risk assessment support, SOP revisions, EN/SICAR management, and CAPA applicabilities

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
• Number of Employees: 5,001-10,000 employees