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Biotech Supply Chain Jobs in Raleigh, NC (NOW HIRING)

Danaher

Director of Operations Strategy

Raleigh, NC · On-site

... biotechnology? At Integrated DNA Technologies (IDT), one of Danaher's 15+ operating companies, our ... Bachelor's degree in Business, Engineering, Operations, Supply Chain, or a related field with 10+ ...

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Biotech Supply Chain information

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How much do biotech supply chain jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for biotech supply chain in Raleigh, NC is $24.45, according to ZipRecruiter salary data. Most workers in this role earn between $18.70 and $27.60 per hour, depending on experience, location, and employer.

What is a biotech supply chain?

A Biotech Supply Chain job involves managing the sourcing, production, and distribution of materials and products used in biotechnology, such as pharmaceuticals, biologics, and medical devices. Professionals in this role ensure that raw materials, laboratory supplies, and finished products move efficiently while complying with strict regulatory standards. They collaborate with suppliers, manufacturers, and logistics teams to optimize costs, minimize delays, and maintain product integrity. Effective supply chain management in biotech is crucial for ensuring that life-saving treatments reach patients safely and on time.

What are some of the main challenges faced in a biotech supply chain role?

Professionals in Biotech Supply Chain often navigate tight regulatory requirements, variable lead times for specialized materials, and the importance of maintaining cold chain logistics for sensitive products. Balancing product quality, traceability, and cost efficiency can be challenging when dealing with highly regulated and rapidly evolving processes. You’ll also frequently collaborate with R&D, quality assurance, manufacturing, and external vendors to ensure products move smoothly from development to distribution. Overcoming these challenges requires attention to detail, proactive communication, and adaptability, making the role both dynamic and rewarding for those who thrive in fast-paced environments.

What are the key skills and qualifications needed to thrive in a biotech supply chain position, and why are they important?

To excel in Biotech Supply Chain, you need strong analytical and organizational skills, industry knowledge of biotechnology supply chains, and often a bachelor’s degree in supply chain management, logistics, or a life sciences field. Expertise with enterprise resource planning (ERP) systems like SAP, as well as familiarity with compliance standards such as GMP or ISO, is usually required. Strong communication, problem-solving, and the ability to collaborate across multidisciplinary teams set top candidates apart. These abilities ensure efficient and compliant supply chain operations, critical for meeting regulatory requirements and delivering biotech products safely and on time.

What are popular job titles related to Biotech Supply Chain jobs in Raleigh, NC?

For Biotech Supply Chain jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Biotech Supply Chain jobs in Raleigh, NC look for?

The top searched job categories for Biotech Supply Chain jobs in Raleigh, NC are:

Biotech Supply Chain jobs near you
Infographic showing various Biotech Supply Chain job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $50,850 per year, or $24.4 per hour.

Senior Manager - Manufacturing Programs - Process Owner Organization

Amgen, Inc.

Holly Springs, NC • On-site

$90K - $116K/yr

Full-time

Re-posted 26 days ago

Job description

Career Category
Manufacturing
Job Description
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like you're part of something bigger, it's because you are. 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. We are global collaborators who achieve together-researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of.
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 single use 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.
Senior Manager - Manufacturing Programs
Live
What you will do
We are seeking a Senior Manager of Manufacturing Programs to lead the Process Owner organization within Manufacturing Support at ANC. This leadership role is responsible for providing technical process stewardship, manufacturing support, process governance, and manufacturing change control support for Upstream, Downstream, and Services Drug Substance Unit Operations.
The Process Owner team serves as the technical process steward for manufacturing operations, partnering closely with Manufacturing Operations and cross-functional support functions to ensure manufacturing processes are effectively governed, implemented, maintained, and continuously improved throughout their lifecycle.
Process Owners serve as the primary technical liaisons between Manufacturing Operations and support organizations including Quality, Engineering, Process Development, Commissioning & Qualification (C&Q), Supply Chain, and Digital Manufacturing. Through floor presence, hypercare support, process ownership, operational readiness activities, and manufacturing change implementation, the team enables reliable, compliant, and efficient manufacturing execution.
The Senior Manager will lead a growing organization of Process Owners responsible for process ownership, floor support and hypercare activities, operational readiness assessments, dry and water run execution, electronic batch record implementation support, manufacturing change implementation, BOM support, and procedural governance. This role will also be responsible for expanding organizational capabilities, including establishing and leading a swing-shift Process Owner team to provide enhanced operational support and manufacturing coverage.
What You Will Do
  • Lead and develop the Process Owner organization responsible for providing technical process stewardship and manufacturing support for Upstream, Downstream, and Services Drug Substance Unit Operations.

  • Provide direct management, coaching, mentoring, and career development for Process Owners.

  • Develop and implement a swing-shift Process Owner organization to provide expanded manufacturing support and floor coverage.

  • Foster a culture of safety, quality, compliance, accountability, collaboration, operational excellence, and continuous improvement.

  • Provide strategic leadership for process ownership, operational readiness, manufacturing change implementation, manufacturing procedures, manufacturing CAPAs, and technical process stewardship.

  • Coordinate with site scheduling to ensure Process Owners provide timely hyper-care support and technical assistance during manufacturing campaigns, startup activities, process changes, first-time executions, and routine operations.

  • Serve as the primary interface between Manufacturing Operations and support organizations including Quality, Engineering, Process Development, C&Q, Supply Chain, and Digital Manufacturing.

  • Oversee execution of dry runs, water runs, engineering runs, and operational readiness activities supporting manufacturing.

  • Own manufacturing-related CAPAs and change controls associated with process, procedural, and operational improvements.

  • Provide leadership and input for electronic batch record (EBR) and manufacturing execution system (MES) implementation activities impacting manufacturing operations.

  • Partner with Technology teams to ensure manufacturing processes are effectively translated into digital workflows and manufacturing execution platforms.

  • Partner with Supply Chain organizations to ensure manufacturing processes, material strategies, and Bill of Materials (BOM) support efficient manufacturing execution.

  • Provide process ownership oversight for BOM creation, maintenance, and updates associated with manufacturing process changes.

  • Ensure creation, revision, maintenance, and periodic review of GMP documentation supporting manufacturing operations.

  • Drive strategic initiatives to improve process reliability, manufacturing efficiency, operator experience, and operational performance.

  • Support inspection readiness activities and represent the Process Owner organization during audits and regulatory inspections as required.

Win
What We Expect of You
Basic Qualifications:
Doctorate degree and 2 years of biotechnology or pharmaceutical industry experience
OR
Master's degree and 6 years of biotechnology or pharmaceutical industry experience
OR
Bachelor's degree and 8 years of biotechnology or pharmaceutical industry experience
OR
Associate's degree and 10 years of biotechnology or pharmaceutical industry experience
OR
High school diploma / GED and 12 years of biotechnology or pharmaceutical industry experience
In addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above
Preferred Qualifications:
  • 8+ years related work experience in biotechnology or pharmaceutical manufacturing with progressively increasing responsibility.

  • Prior people leadership experience managing and developing technical teams.

  • Strong understanding of GMP manufacturing operations supporting Upstream, Downstream, and Services Drug Substance Unit Operations.

  • Experience with process ownership, manufacturing support, and technical process stewardship.

  • Experience supporting digital manufacturing systems, electronic batch records (EBRs), manufacturing execution systems (MES), and associated process implementation activities within a GMP manufacturing environment.

  • Experience authoring, approving, and governing manufacturing SOPs and GMP documentation within Quality Systems (i.e. Veeva, Documentum, etc.).

  • Experience leading manufacturing CAPAs/change controls and implementation activities.

  • Experience supporting operational readiness activities, including dry runs, water runs, process implementation, and startup support.

  • Experience partnering with Supply Chain organizations to support BOM management, material readiness, and manufacturing execution.

  • Excellent organizational, written, verbal communication, and cross-functional leadership skills.

Salary Range
154,173.00USD -208,587.00 USD

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