Manufacturing Manager Programs – Cleaning Validation

Regulatory Jobs

Holly Springs (NC)

On-site

USD 130,000 - 190,000

Full time

2 days ago
Be an early applicant
Application generator

Get a reply from this employer — a resume and cover letter tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Career development resources
Diversity & inclusion
Total rewards plan

Job summary

Amgen seeks a senior validation leader for the North Carolina manufacturing site. The role leads the cleaning/sterilization validation program, develops the Validation Master Plan, and ensures readiness for regulatory filings and inspections.

You will oversee design and execution of validation strategies, coordinate with cross-functional teams, and drive continuous improvement in validation processes while maintaining compliance with FDA regulations.

Qualifications

  • Doctorate degree OR Master’s degree with 3+ years of Validation/Engineering experience.
  • In addition to degree requirements, must have experience directly managing people or leadership roles.
  • Proficient technical writing and presentations skills to collaborate with technical and senior management.

Responsibilities

  • Lead team responsible for cleaning validation and sterilization programs at ANC.
  • Provide technical support for commissioning, qualification, cleaning/sterilization validation, and maintenance activities.
  • Collaborate with project leads on validation outputs for equipment commissioning and qualification.
  • Prepare and review cleaning-related documents (e.g., validation reports, acceptance limits).
  • Coordinate with Manufacturing, Engineering, Quality, Supply Chain, and Process Development to meet validation requirements.

Skills

Leadership
Technical writing
Validation expertise
Project management

Education

Doctorate degree
Master’s degree
Bachelor’s degree

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.

Manufacturing Manager Programs – Cleaning Validation

Live

What you will do

Let’s do this. Let’s change the world. In this vital role the Senior Engineer-Validation will serve as a technical lead/subject matter expert (SME) and lead the development and implementation of the Validation strategy at the Amgen North Carolina (ANC) manufacturing facility. Specifically, this role has responsibility for developing and generating documents such as the site’s Validation Master Plan, validation plans, equipment qualification protocols/reports, among others. In addition, the position will be accountable for completing landmarks related to results for autoclave performance qualification, cleaning validation, and validation maintenance.

Responsibilities:

  • Lead a team responsible for implementing and maintaining the facility cleaning validation and sterilization program.
  • Provide technical support and domain expertise for commissioning, qualification, cleaning/sterilization validation, and validation maintenance activities in ANC
  • Collaborate with project leads with direct accountability for project results related to validation outputs for commissioning and qualification of manufacturing process equipment
  • Supply cleaning/sterilization validation expertise including generation/review/approval of cleaning related documents (e.g., cleaning characterization/inactivation reports, acceptance limits reports)
  • Coordinate actions with Manufacturing, Engineering, Quality, Supply Chain, and Process Development to ensure that the overall Amgen validation requirements are met
  • Furnish technical assistance and represent validation for regulatory filings, audits, and inspections
  • Ensure maintenance of site validation master plan and routine monitoring of validation status/regulatory compliance of equipment and systems
  • Support site/network validation driven continuous improvement initiatives

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek will possess these qualifications.

Basic Qualifications

Doctorate degree OR

Master’s degree and 3 years of Validation or Engineering experience OR

Bachelor’s degree and 5 years of Validation or Engineering experience OR

Associate’s degree and 10 years of Validation or Engineering experience OR

High school diploma/GED and 12 years of Validation or Engineering experience

AND In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, prograns, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications

  • Experience managing staff executing technical skills in a safe and compliant manner.
  • Proficient technical writing and presentations skills so as to collaborate with technical and senior management staff
  • Expertise in equipment qualification & cleaning validation (including establishing validation strategies and procedures) for biologics facility
  • Extensive experience in reviewing/approving validation protocols and reports in support of facility/equipment commissioning, qualification, and change administration
  • Involvement in technical implementation of validation tasks associated with cleaning validation, steaming validation (including autoclaves) and controlled temperature chambers (CTC)
  • Knowledge of Regulations Eudralex Annex 15, FDA Title 21 CFR Part 210 and 211, Guidelines ASTM E2500 and ICH Q7
  • Participation in supporting regulatory submissions, response to submission questions, pre-approval/biennial inspections, and observational response plans

Thrive

Some of the vast rewards of working here

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

  • Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
  • A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Amgen requires all staff in the United States and Puerto Rico to be vaccinated from COVID 19 as a condition of employment. In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff.

Salary Range

USD -USD
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Manufacturing Manager Programs – Cleaning Validation
Manufacturing Manager Programs – Cleaning Validation

Amgen SA • Holly Springs (NC), Northern (KY)

Hybrid
USD 140,000 - 190,000
Career development resources
Total rewards plan
Manufacturing Manager Programs – Cleaning Validation
Manufacturing Manager Programs – Cleaning Validation

Amgen Inc. (IR) • Holly Springs (NC)

On-site
USD 140,000 - 190,000
Manufacturing Programs Senior Manager: Cleaning Validation
Manufacturing Programs Senior Manager: Cleaning Validation

amgen • Holly Springs (NC)

Hybrid
USD 136,000 - 184,000
Total Rewards Plan
Stock-based incentives
Flexible work model
Manufacturing Programs Senior Manager: Cleaning Validation
Manufacturing Programs Senior Manager: Cleaning Validation

Amgen Inc. (IR) • Holly Springs (NC)

On-site
USD 136,000 - 184,000
Comprehensive benefits
Retirement plan
Medical coverage
+9
Validation Engineer I
Validation Engineer I

Amgen • Holly Springs (NC)

On-site
USD 110,000 - 150,000
Retirement & Savings Plan
Group medical/dental/vision coverage
Life and disability insurance
+5
Specialist Manufacturing – Cleaning Validation
Specialist Manufacturing – Cleaning Validation

Amgen Inc. (IR) • Thousand Oaks (CA)

On-site
USD 108,000 - 146,000
Stock-based incentives
Flexible work models
Retirement and savings plan
Associate Mfg Systems Engineer I
Associate Mfg Systems Engineer I

Amgen • Holly Springs (NC)

On-site
USD 110,000 - 140,000
Retirement plan
Medical/dental/vision coverage
Bonus program
+3
Specialist Manufacturing – Cleaning Validation
Specialist Manufacturing – Cleaning Validation

Amgen SA • Thousand Oaks (CA)

On-site
USD 110,000 - 160,000
Validation Engineer
Validation Engineer

amgen • West Greenwich (RI)

On-site
USD 86,000 - 116,000
Retirement plan
Stock options
Discretionary bonus
+1
Senior Associate - Bulk Drug Substance Manufacturing Services - Days
Senior Associate - Bulk Drug Substance Manufacturing Services - Days

Amgen • Holly Springs (NC)

On-site
USD 65,000 - 95,000
Flexible work models
Discretionary annual bonus
Stock-based long-term incentives
+1