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Technical Process Leader Jobs (NOW HIRING)

Merck & Co.

$101K - $131K/yr

The successful candidate will provide technical leadership and process ownership supporting facility design, commissioning, qualification, and startup through to technology transfer, validation, and ...

RESILIENCE

Process Engineer II

West Chester, OH · On-site

Validation & Technical Support * Leads validation activities for assigned processes, defining success criteria, confirming process capability, and maintaining validated state through change.

Resilience

Process Engineer II

West Chester, OH · On-site

Validation & Technical Support * Leads validation activities for assigned processes, defining success criteria, confirming process capability, and maintaining validated state through change.

RESILIENCE

Process Engineer II

West Chester, OH · On-site

Validation & Technical Support * Leads validation activities for assigned processes, defining success criteria, confirming process capability, and maintaining validated state through change.

Resilience

Validation & Technical Support Leads validation activities for assigned processes, defining success criteria, confirming process capability, and maintaining validated state through change. Authors ...

Resilience

Initiates deviations and independently leads technical investigations and impact assessments for assigned processes.Authors and reviews controlled documents including SOPs, Batch Records, and Rework ...

8 Rivers

Senior Process Engineer

Durham, NC · On-site

$100K - $130K/yr

... industry-leading companies to develop and deploy those technologies. Our process enables us to ... Draft technical documentation including white papers, patents, and specifications to protect ...

8 Rivers

Senior Process Engineer

Durham, NC · On-site

$94K - $121K/yr

Draft technical documentation including white papers, patents, and specifications to protect ... Partner with industry leaders and global vendors to seamlessly integrate proprietary 8 Rivers ...

Fike

Buyer III

Blue Springs, MO · On-site

$67K - $84K/yr

The Buyer 3 influences sourcing, replenishment, and inventory decisions; leads supplier negotiations and contracts; and serves as a technical and process leader within the Purchasing function.

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How much do technical process leader jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for technical process leader in the United States is $34.67, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $46.63 per hour, depending on experience, location, and employer.

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Infographic showing various Technical Process Leader job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $72,110 per year, or $34.7 per hour.

Specialist Manufacturing - Process Owner - Upstream / Downstream / Services

Holly Springs, NC • On-site

Amgen
See more jobs at Amgenexternal

$63K - $84K/yr

Other

Re-posted 2 days ago

Job description

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 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 USD

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