Senior Associate Manufacturing – Manufacturing Investigations

Amgen

Holly Springs (NC)

On-site

USD 86,000 - 116,000

Full time

14 days+

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Benefits offered by this job

Retirement and savings plan
Stock-based incentives
Flexible work arrangements

Job summary

Amgen Inc. (IR) in North Carolina seeks a Senior Associate Manufacturing – Manufacturing Investigations Live to investigate deviations at a biologics Drug Substance plant.

You will interface with GMP teams, Process Development, Facilities, and Quality to ensure investigations are conducted and documented, driving process improvements. The role requires experience in biologics manufacturing, environmental monitoring, and cross-functional project management, with strong communication skills and

Qualifications

  • High School Diploma or GED with relevant manufacturing/regulatory experience.
  • Associate’s Degree with 2+ years in a regulated environment or manufacturing.
  • Bachelor’s Degree with 6 months in manufacturing or regulated environment.
  • Master’s Degree preferred for advanced roles.

Responsibilities

  • Manage deviation and environmental monitoring investigations, lead root cause analysis, develop CAPAs, document findings.
  • Apply microbiology principles to environmental monitoring investigations and contamination control.
  • Interpret monitoring data, identify trends, assess impact on product quality and operations.
  • Present investigations to regulators, auditors, and leadership; communicate progress to stakeholders.
  • Lead cross-functional teams to complete milestones on schedule; write clear technical reports.

Skills

Deviation investigations
CAPA
Environmental monitoring
Root cause analysis
GMP knowledge

Education

Bachelor's Degree + 6 months manufacturing and/or other regulated environment experience
Associate’s Degree + 2 years manufacturing and/or other regulated environment experience
High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience
Master's Degree

Tools

Veeva QMS

Job description

Senior Associate Manufacturing – Manufacturing Investigations Live

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.

What you will do

In this vital role, you will be a key member of the team that investigates major deviations in the Amgen North Carolina Biologics Drug Substance Manufacturing plant. You will communicate and interface between the GMP manufacturing teams and stakeholder groups including, Process Development, Facilities & Engineering, Automation, EHSS, and Quality. This position is responsible for ensuring deviation investigations are successfully conducted and documented while driving improvements in the investigation process.

Responsibilities
  • Manage simple deviation and environmental monitoring investigations, specifically within the Controlled Environmental Monitoring space, leading root cause analysis, development of CAPAs, and compliant documentation of all findings.
  • Apply a basic understanding of microbiology principles, environmental monitoring programs, and contamination control strategies to support environmental monitoring investigations.
  • Interpret environmental monitoring data, identify trends, and assess potential impacts to product quality, manufacturing operations, and contamination control programs.
  • Present investigations to regulatory inspectors, internal auditors, and management.
  • Clearly communicate investigation progress to impacted areas and leadership.
  • Coordinate and effectively lead cross‑functional teams through investigations, and complete milestones on‑schedule.
  • Present investigation findings and technical information to diverse audiences and communicate moderately complex issues in a clear and concise manner.
  • Build effective relationships across functions.
  • Navigate through ambiguity and provide a structured problem‑solving approach.
  • Apply inductive and deductive reasoning in the investigation process.
  • Clear and concise technical writing.
  • Use Operational Learning Team strategies to promote open collaboration with staff to maximize investigation findings.
  • Develop tracking tools to ensure on‑time closure and proactive review of deviation investigations.
Win What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The collaborative investigator we seek has a biologics Drug Substance manufacturing and microbiological investigations background with strong cross‑functional project management and communication skills as well as the below qualifications.

Basic Qualifications
  • High School Diploma/GED + 4 years manufacturing and/or other regulated environment experience
  • Associate’s Degree + 2 years manufacturing and/or other regulated environment experience
  • Bachelor’s Degree + 6 months manufacturing and/or other regulated environment experience
  • Master's Degree
Preferred Qualifications
  • 3+ years related work experience (manufacturing, microbiology, process development, or quality assurance) in biotech or pharmaceutical industry with progressively increasing responsibility
  • Basic understanding of Drug Substance manufacturing, environmental monitoring programs, and contamination control principles.
  • Experience with compliance, problem‑solving, simple and complex root cause analysis tools (5-whys, fishbone etc.) critical thinking, project management, and quality systems.
  • Degree in Science or Engineering (Microbiology or similar a plus)
  • Experience leading investigations
  • Experience using Veeva QMS for Deviation investigations and CAPAs
  • Demonstrated project management ability
  • Excellent written and verbal communication skills
  • Ability to work in a team matrix environment and build relationships with partners
  • Strong interpersonal skills
  • Thrive
What you can expect of us
  • Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
  • A discretionary annual bonus program, or for field sales representatives, a sales‑based incentive plan
  • Stock‑based long‑term incentives
  • Award‑winning time‑off plans and bi‑annual company‑wide shutdowns
  • Flexible work models, including remote work arrangements, where possible

Salary Range 86,048.05USD -116,417.95 USD

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 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 accommodation. #AmgenNorthCarolina .

A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen

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