Senior Associate Manufacturing - Bulk Drug Substance Downstream - Nights

HOW MIGHT YOU DEFY IMAGINATION? 

You’veworked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills,experience,and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over10 million patientsworldwide. Come do your bestworkalongside other innovative, driven professionals in this meaningful role.

Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the AmgenFleXBatch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. TheFleXBatch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.

Senior AssociateManufacturing- Bulk Drug Substance Downstream-Nights

Live

What youwill do

Let’sdo this.Let’schange the world. In this dynamic role,you will beaSenior Associate inthemanufacturing organization atAmgenNorth Carolina (ANC). The essential position, which supports our critical 24/7 manufacturing operations, works a 12-hour 2-2-3 schedule from 5:45pmto6:15am. Associates will be executing operations on the floorin our downstream       area and will be responsible for the manufacturing of cGMP (Current Good Manufacturing Practices) drug substances.  

With general direction, the Senior Associate is responsible for executing on-the-floor operations within manufacturing in accordance with cGMP practices. As Amgen relies upon the regular attendance of staff members to meet legitimate business needs, staff must be able to work assigned 12-hour shift, including during inclement weather, some holidays and requested overtime in support of our 24/7 operations.  

Responsibilitieswill include…

Compliance: 

• Completes workin accordance withestablished 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 non-conformance (NC) reports 

• Interact with regulatory agencies asneeded andguided

• Assure proper gowning and aseptic techniques arealways followed

Process/Equipment/Facilities: 

• Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)

• Perform hands-ondownstream biotechoperations(Column Chromatography, Tangential Flow Filtration, Viral Filtration, Viral Inactivation, Column Packing among others)including set-up,operation,cleaning, sanitization,monitoringof equipment and assigned area

• Runandmonitorcritical process tasksperassigned procedures

• Perform in-process sampling,operateanalytical equipment, andcompleteprocess documentation(ElectronicBatchRecords[EBR])

• Completewashroom activities:cleaning equipment, small to large scale, used in production activities

• Initiate and own manufacturing relatedprocessdeviations

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

• Assistin the review ofdocumentation for assigned functions (i.e.,equipment logs,EBRs)

• Collaborateas part of across-functional team (i.e.,QA/QC,F&E (Facilities & Engineering), PPIC,Mfg.,PD (Process Development), Regulatory, etc.) in completing production activities

• Responsible forrecognizing andelevating 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, andassistthe 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 managementas an advisorin planningandinescalatingpotential concerns withtheschedule and/or process

Win

What we expectofyou

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

Basic Qualifications:

• HighSchoolDiploma/GED + 4yearsmanufacturing and/orotherregulatedenvironmentexperience 

Or​

• Associate’sDegree+ 2 yearsmanufacturing and/orotherregulated environment experience 

Or​

• Bachelor’sDegree+ 6 monthsmanufacturing and/orotherregulatedenvironmentexperience 

Or

• Master's ​Degree

Preferred Qualifications:

• Completion of NCBioWorksCertification Program

• Experience in biotechnology or pharmaceuticalplant start up 

• Knowledge andprocessexperience within a cGMP manufacturingfacility or other highlyregulated environment 

• Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)

• 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

Thrive

What you can expectofus

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being. 

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.

Amgen offers a Total Rewards Plancomprisinghealth and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including: 

• 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 and bi-annual company-wide shutdowns 

• Flexible work models, including remote work arrangements, where possible

Apply now