Specialist Manufacturing – Process Owner - Upstream / Downstream / Services
Company websiteamgen.com (Amgen, opens in new tab)
Base salary $107,545 to $145,503
Employer-published annual base salary, USD. Advertised base range in Holly Springs, NC
You apply on the employer's own site. Six Figure Work does not handle applications.
- LocationHolly Springs, NC
- WorkplaceOn-site
- Status at last checkSource accepting applications when checked
- Last checked (2 min ago) · observed since
About this job
Career Category
ManufacturingJob Description
HOW MIGHT YOU DEFY IMAGINATION?
You’ve worked 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 over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.
Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX Batch facility will combine the latest in disposable technologies with traditional stainless-steel equipment to allow for maximum flexibility in operations. The FleX Batch 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.
Specialist Manufacturing – Process Owner - Upstream / Downstream / Services (Multiple Positions)
Live
What You Will Do
In this vital role, you will serve as a Process Owner within the Manufacturing Support organization at Amgen North Carolina (ANC). The Process Owner serves as a technical process steward and key interface between Manufacturing Operations and support organizations. This role is responsible for supporting manufacturing execution through technical process ownership, floor support, operational readiness activities, process governance, manufacturing change implementation support, and continuous improvement initiatives.
This position may support one of the following manufacturing areas depending on business needs and organizational assignment: Upstream Manufacturing, Downstream Manufacturing, or Manufacturing Services (Raw Material Dispensing and Solution Preparation).
Serve as the technical process owner for assigned manufacturing processes, equipment, and unit operations.
Provide manufacturing floor support, troubleshooting assistance, and hypercare during routine manufacturing operations, process changes, startup activities, and first-time executions.
Support operational readiness activities including water runs, dry runs, equipment readiness verification, and Electronic Batch Record (EBR) testing support.
Partner with Manufacturing Operations to support reliable, compliant, and efficient manufacturing execution.
Monitor process performance and identify opportunities for process optimization, operational improvement, and risk reduction.
Support manufacturing-related change controls associated with process, equipment, procedural, and operational improvements.
Author, revise, review, and maintain manufacturing SOPs, forms, and other GMP documentation.
Ensure manufacturing processes are effectively translated into SOPs, manufacturing workflows, training materials, and associated digital manufacturing processes.
Provide technical input to manufacturing risk assessments and support identification and mitigation of process, equipment, procedural, and operational risks.
Participate in root cause analysis (RCA) activities and provide technical process expertise to support manufacturing investigations, major deviations, and quality events.
Support CAPA applicability assessments, CAPA implementation activities, and CAPA effectiveness checks.
Partner with Process Development to support process overviews, knowledge transfer activities, and facility fit assessments.
Partner with Supply Chain, Manufacturing, and Engineering to support material readiness and Bill of Material (BOM) alignment, including single-use assemblies and consumables.
Support MES and EBR activities by providing process expertise and manufacturing representation.
Participate in inspection readiness activities and support audits as required.
Appropriately escalate process, operational, quality, and compliance concerns.
Win
What We Expect of You
Basic Qualifications
Doctorate degree and 2 years of biotechnology operations experience OR
Master's degree in Engineering, Biology, Chemistry, Biochemistry, or related field and 4 years of biotechnology operations experience OR
Bachelor's degree and 6 years of biotechnology operations experience OR
Associate's degree and 10 years of biotechnology operations experience OR
High school diploma / GED and 12 years of biotechnology operations experience
Preferred Qualifications
Technical expertise in Upstream Manufacturing, Downstream Manufacturing, or Manufacturing Services (Raw Material Dispensing and Solution Preparation).
Strong technical knowledge of drug substance manufacturing processes, equipment, and unit operations.
Experience supporting GMP manufacturing operations in a biotechnology or pharmaceutical environment.
Experience supporting manufacturing floor operations, troubleshooting, and hypercare activities.
Experience supporting operational readiness activities including water runs, dry runs, equipment testing, and startup support.
Experience authoring and maintaining GMP documentation including SOPs and manufacturing procedures.
Experience supporting manufacturing change controls and implementation activities.
Experience participating in risk assessments, root cause analyses, investigations, and CAPA implementation activities.
Experience supporting CAPA applicability assessments and effectiveness checks.
Experience supporting Manufacturing Execution Systems (MES) and Electronic Batch Records (EBRs) within a GMP manufacturing environment.
Knowledge of single-use technologies and Bill of Material (BOM) structures.
Strong technical writing, communication, problem-solving, and organizational skills.
Thrive
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 through comprehensive benefits, career development opportunities, and a collaborative culture.
.Salary Range
107,545.40USD -145,502.60 USDSource: Amgen on Workday · View original posting (opens in new tab)
Pay in context
This role's base floor ($107,545) is above 11% of the 1,148 Manufacturing & Production roles nationwide listed on this site; 2 others list the same floor. Their median floor is $136,000; the middle half runs from $117,450 to $158,000.
Only jobs on this site count, and each one publishes a base salary of $100,000 or more, so this compares six-figure jobs with each other, not with the whole market. Computed Nov 7, 2026.
This listingSpecialist Manufacturing – Process Owner - Upstream / Downstream / Services$107,545 to $145,503
Project Manager, Congress Planning$110,031 to $148,865
Specialist IS Business Systems Analyst$110,038 to $148,876
Program Manager$109,641 to $148,337
Manager - Business Operations Partner - Neurology & IgG4-RD$109,641 to $148,337
Scientist - LC-MS Bioanalytical$109,020 to $147,498
Scientist, Immunogenicity Bioanalytical$109,020 to $147,498
Chart as a table
| Role | Published base |
|---|---|
| Specialist Manufacturing – Process Owner - Upstream / Downstream / Services (this listing) | $107,545 - $145,503 |
| Project Manager, Congress Planning | $110,031 - $148,865 |
| Specialist IS Business Systems Analyst | $110,038 - $148,876 |
| Program Manager | $109,641 - $148,337 |
| Manager - Business Operations Partner - Neurology & IgG4-RD | $109,641 - $148,337 |
| Scientist - LC-MS Bioanalytical | $109,020 - $147,498 |
| Scientist, Immunogenicity Bioanalytical | $109,020 - $147,498 |
Observed changes
- First observed on the employer's board
- Began meeting the published-salary criteria
- Observed since
- Employer-stated posting date
- 2026-08-17
Where this pay comes from
Location as the employer wrote it: US - North Carolina - Holly Springs
107,545.40USD -145,502.60 USD
- Method
- Employer text, read with fixed rules and re-verified
- Checked
- Rule set
- us-base-v2
The pay passage appears in the employer's own job text. Fixed, deterministic rules located it, and the passage below was checked against the stored copy of the posting.
What we verified
- The pay figures come from the employer's own listing, quoted exactly above.
- The pay is an annual base salary in US dollars with a minimum of at least $100,000.
- The role was publicly listed on the employer's job board when last checked.
We do not verify what the employer will actually offer, whether the employer is still recruiting for the role, or anything beyond what the employer published. Full methodology.
