Senior Associate Manufacturing - Bulk Drug Substance Upstream - Days

Senior Associate Manufacturing - Bulk Drug Substance Upstream - Days

What you will do

Let’s do this! Let’s change the world! In this dynamic role, you will be anSenior Associate in the manufacturing organization at Amgen North Carolina (ANC) supporting the facility expansion program and facility startup. This essential role will be part of a team responsible for manufacturing cell culture operationsincluding seed train, SUBs, Perfusion, RTF, Stainless Steel BRXs, Depth Filtration and Centrifugation,while partnering across functions to ensure successful operational readiness, technology transfer, and ramp‑up of manufacturing operations within the new facility.

This role may require work outside standard business hours, including non‑standard shifts, as needed to support startup, commissioning and qualification (C&Q), and engineering execution.  During this phase of the startup, you will be expected to work a Monday – Friday schedule from 8am – 5pm.As the business moves from C&Q to manufacturing operations, this essential positionwillwork ona 12-hour 2-2-3 schedule from 5:45 am to6:15pmsupporting our critical 24/7 manufacturing operations.As Amgen relies upon the regular attendance of all staff members to meet legitimate business needs, this role must be able to work assigned 12-hourshift, including during inclement weather, some holidays and requested overtime in support of our operations.

During early phases, this role will focus on operational readiness, training, and startup execution. As the facility transitions to steadystate operations, the role will shift toward routine manufacturing execution and continuous improvement.

Compliance:

Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance

Initiate Quality observations (Discrepancies, Deviations, Testing Results Analysis (TRA), etc.) as well as support or lead evaluations and investigations into quality observations

Interact with regulatory agencies as needed and guided

Assure proper gowning and aseptic techniques are always followed

​

Operational Readiness & Facility Startup

Support operational readiness activities for facility expansion and startup

Execute manufacturing readiness tasks including equipment preparation, procedure execution, and process walkthroughs

Participate in commissioning, qualification, and startup activities as trained and assigned

Provide operational feedback during startup activities to support safe, compliant, and efficient manufacturing

Support readiness planning through execution of training, procedures, workflows, and operational practices required for startup and ramp‑up

​

Process/Equipment/Facilities:

Perform hands-on operations including set-up, cleaning, sanitization, monitoring of equipment of assigned area

Run and monitor critical process tasks per assigned procedures

Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBR])

Complete washroom activities: cleaning equipment, small to large scale, used in production activities

Identify, recommend, and implement innovative process improvements and optimizations related to daily routine functions

Assist in the review of documentation for assigned functions (i.e., equipment logs, EBRs, ESPs)

Collaborate cross-functionally (i.e., QA/QC, F&E (Facilities & Engineering), PPIC (Production Planning and Inventory Control), Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

Responsible for recognizing and elevating problems during daily operations

Participate in the implementation of programs and CAPAs (Corrective Action Preventive Action) with an eye toward continuous improvement

Drive safety in all operations, and assist the manager in escalating concerns as needed

Maintain an organized, clean, and workable space

Administrative:

Draft and revise documents (SOPs, technical reports, and MPs)

Interacts with management as an advisor in planning and in escalating potential concerns with the schedule and/or process

​

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The hard-working professional we seek is a team player with these qualifications.

Basic Qualifications:

High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience OR

Associate’s Degree + 2 years manufacturing and/or other regulated environment experience OR

Bachelor’s Degree + 6 months manufacturing and/or other regulated environment experience OR

Master's Degree

​

Preferred Qualifications:

Completion of NC BioWork Certificate Program

Experience in biotechnology or pharmaceutical plant start up

Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment

Basic understanding of Upstream operation (Vial Thaw, Inoculation/Cell Expansion, Single Use Bioreactor, Production Bioreactor, ATF, Harvest Centrifuge, Depth Filtration)

Excellent verbal and written communication (technical) skills

Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems

​

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.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

.

Salary Range

86,048.05USD -116,417.95 USD