Sr. Associate, Manufacturing 12 hour Shift (Evenings 6pm-6am)

Amgen Inc. (IR); New Albany (OH); Hybrid; USD 86,000 - 116,000; Full time

Benefits offered by this job

Retirement plan

Medical/Dental/Vision coverage

Life & Disability insurance

Bonus program

Stock-based incentives

Paid time off (PTO)

Flexible work models

Job summary

Amgen Inc. (IR) in the United States is seeking a Manufacturing Senior Associate to manage and lead a device assembly and packaging line, ensuring full cGMP compliance and timely production.

The role involves supervising technicians, equipment setup, troubleshooting, and safety adherence across the manufacturing floor. The candidate will collaborate with Quality, Engineering and Manufacturing Support, drive continuous improvement, and participate in deviations, CAPA, and change controls.

Qualifications

• High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience
• Or Associate’s + 2 years biotech or pharmaceutical manufacturing, process development or quality experience
• Or Bachelor’s + 6 months biotech or pharmaceutical manufacturing, process development or quality experience
• Or Master’s degree may substitute for experience when applicable
• Degree in Chemical/Industrial Engineering or Life Sciences is preferred
• Experience with cGMP and pharmaceutical/biotech packaging equipment is desirable
• Experience leading cross-functional teams and managing multiple priorities

Responsibilities

• Manage and lead device assembly & packaging line operations.
• Maintain production in full cGMP compliance.
• Supervise and develop technicians and oversee equipment to meet production schedules.
• Lead floor manufacturing operations including equipment setup, operation and troubleshooting.
• Provide training and technical support on processes and equipment.
• Collaborate with Quality, Engineering and Manufacturing Support to resolve events.
• Support CAPA, deviations, and change controls.
• Write and revise SOPs and manufacturing documents.

Skills

Cross-functional teamwork

Change management

Problem solving

Communication

Education

Bachelor's in Chemical Engineering

Bachelor's in Industrial Engineering

Bachelor's in Life Sciences

Tools

MES

LIMS

Maximo

CCMS

SAP

Job description

Career Category Manufacturing Job Description 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. 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.

Manufacturing Senior Associate

What you will do

Let’s do this. Let’s change the world. In this role you will be managing and leading all aspects of a device assembly & packaging line.

• Responsibility includes maintaining production in full cGMP compliance.
• Assist with supervising and developing technicians while overseeing production equipment to ensure production schedules are completed.
• Lead manufacturing operations on the production floor while helping to perform equipment setup, operation and troubleshooting.
• Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.
• Ensure all safety and compliance procedures are followed at all times.
• Escalate appropriate concerns to various levels of management when personnel and environmental safety, equipment functionality, product supply, or quality are at risk.
• Provide training to manufacturing staff on process and equipment.
• Provide troubleshooting, technical support, and resolution of equipment, automation, and process issues on the manufacturing floor.
• Collaborate with Quality, Engineering and Manufacturing Support to resolve manufacturing events in a timely manner.
• Support Deviation Triage and Corrective and Preventive Actions (CAPA) processes
• Write, review & revise controlled documentation (SOPs, Manufacturing Procedures (MPs), Forms, Technical Reports, etc)
• Apply process, scientific, operational, and compliance knowledge with analytical and troubleshooting skills to support manufacturing operations.
• Champion Lean Transformation and OE initiatives, facilitate the drive towards continuous improvement in the plant.
• Participate in the design, development, and implementation of processes in support of the manufacturing floor.
• Participate in the development, implementation, and issue resolution associated with process equipment Commissioning, Qualification and Validation.
• Collaborate with Quality, Mfg Managers, Plant Engineering, Process Development and Regulatory Compliance staff in cross‑functional teams.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The manufacturing professional we seek will possess these qualifications.

Basic Qualifications:

• High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience
• Or Associate’s + 2 years biotech or pharmaceutical manufacturing, process development or quality experience
• Or Bachelor’s + 6 months biotech or pharmaceutical manufacturing, process development or quality experience work experience
• Or Master’s

Preferred Qualifications:

• Degree in Chemical Engineering, Industrial Engineering or Life Sciences
• Technical understanding of pharmaceutical/biotech packaging equipment and processes
• Experience with Current Good Manufacturing Practices (cGMP)
• Ability to be flexible and manage change
• Experience participating in and leading cross‑functional teams
• Experience in managing multiple, competing priorities in a fast‑paced environment
• Strong scientific, technical interactions with partner organizations such as PD and F&E.
• Experience in GMP Tech Support roles, GMP operations, process development or scheduling.
• Experience with Commissioning and Qualification, New Product Introduction, Cleaning Validation, and Process Performance Qualification
• Ability to organize, analyze, and interpret technical data that is impacting operations
• Background in lean manufacturing methodologies and operational excellence
• Expertise in electronic systems used in manufacturing (MES, LIMS, Maximo, CCMS, SAP, etc.)

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well‑being.

From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

• 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, including remote and hybrid work arrangements, where possible

Salary Range 86,048.05USD -116,417.95 USD

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is a Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

For more information, visit www.amgen.com and follow us on www.twitter.com/amgen