Biogen

Biogen

Sr Associate I, Quality Control Microbiology

Research Triangle Park, NC, USA · Senior

Sponsorship not specified$81k-$105kDetected 1 day ago
ExcelProcess ImprovementClinical Laboratory TechniquesGMPCommunicationOrganizational SkillsMicrosoft Office

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odds of building a lasting career here

48Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role82
Entry-level history0
PERM / green-card track0
Lottery odds (Level II)66
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~30% per draw at Level II). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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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 7 green-card filings in this occupation, 100% were for a worker who already held the job.

Files H-1B transfers

14 transfer filings in the last year, covering 14 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

  • Associate I is responsible for leading key operational aspects of the QC Microbiology laboratory.
  • Additionally this role is responsible for method qualification and projects as assigned.

Responsibilities

  • Supports testing for all qualification and study directed testing
  • Perform microbiology testing (e.g. Bioburden, Endotoxin, plate reading, and microbial identification) following standard procedures
  • Comply with SOPs and controlled documents under minimal supervision
  • Maintain laboratory cleanliness, equipment readiness, and inventory
  • Perform investigations (i.e. laboratory and deviations)
  • Perform other assigned duties

Requirements

  • Bachelor's in Microbiology, Biology, or related field
  • Minimum 4 years' experience in pharmaceutical microbiology and GMP-regulated manufacturing
  • Demonstrated knowledge of microbiological assays (bioburden, endotoxin, environmental monitoring), aseptic techniques, and general laboratory techniques
  • Experience with document control including reviewing and editing technical documents
  • Strong written and verbal communication skills, along with proficiency in Microsoft Word and Excel
  • Excellent organizational skills with the ability to prioritize, follow through on tasks, and meet deadlines
  • Work overtime as required by business needs

Nice to have

  • Preferred Skills

Compensation

  • Tuition reimbursement of up to $10,000 per calendar year

Benefits

  • Medical, Dental, Vision, & Life insurances
  • Paid Maternity and Parental Leave benefit
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Employee stock purchase plan
  • Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Company info

  • We are a global team with a commitment to excellence, and a pioneering spirit.
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 401(k) program participation with company matched contributions
  • As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact.

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