Amgen

Amgen

Senior Associate Manufacturing - Bulk Drug Substance Downstream - Days

US - North Carolina - Holly Springs · Senior

Sponsorship not specifiedDetected 71 days ago
GMPResearchCommunicationMicrosoft Office

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odds of building a lasting career here

38Risky
Cap-exempt (no lottery)0
Sponsors this role85
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 101 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 92%

Of 75 labor certifications old enough to have been used, 6 expired without the employer filing the next step. Median time from filing to decision: 486 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Files H-1B transfers

17 transfer filings in the last year, covering 17 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • Join Amgen's Mission of Serving Patients
  • At Amgen, if you feel like you're part of something bigger, it's because you are.
  • Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases.

Responsibilities

  • Perform hands-on downstream biotech operations (Column Chromatography, Tangential Flow Filtration, Viral Filtration, Viral Inactivation, Column Packing among others) including set-up, operation, cleaning, sanitization, monitoring of equipment and assigned area
  • Perform in-process sampling, operate analytical equipment, and complete process documentation (Electronic Batch Records [EBR])
  • Initiate and own manufacturing related process deviations
  • Identify, recommend, and implement innovative process improvements and optimizations related to daily routine functions

Requirements

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

Nice to have

  • Completion of NC BioWorks Certification Program
  • Experience in biotechnology or pharmaceutical plant start up
  • Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment
  • Understanding of downstream purification operation (Column Chromatography, TFF, Viral Filtration, Viral Inactivation)
  • Excellent verbal and written communication (technical) skills
  • Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems
  • What you can expect of us
  • careers.amgen.com

Compensation

  • 86,048.05USD -116,417.95 USD

Company info

  • Career Category Manufacturing Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are.
  • If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team.
  • Be part of Amgen's newest and most advanced drug substance manufacturing plant.
  • Collaborate as part of a cross-functional team (i.e., QA/QC, F&E (Facilities & Engineering), PPIC, Mfg., PD (Process Development), Regulatory, etc.) in completing production activities

This listing is sourced directly from Amgen's careers page and normalized into a canonical job model.