Specialist Manufacturing – Process Owner - Upstream / Downstream / Services
Notify me about similar jobsAbout this opportunity
Career Category
Manufacturing
Job 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 initi atives.
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 USD
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 3672 comparable Manufacturing & CMC roles across 170 biopharma companies.
Salary context
898 of 3672 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 3672 comparable roles
+ 54 more countries
Seniority mix
1627 of 3672 peers have a known seniority level
Therapeutic area mix
24 of 3672 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
Or follow a whole field: get every new Manufacturing & CMC job in the United States, and choose locations and companies.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.