Ophthalmic QC Microbiology & Stability Scientist

Harrow, Inc.

Ledgewood (NJ)

On-site

USD 65,000 - 95,000

Full time

14 days+
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Job summary

Harrow, Inc. seeks a QC Microbiology professional to oversee routine and non-routine testing, data review, and stability program management in support of GMP manufacturing.

You will handle environmental monitoring, microbial testing, deviations, CAPAs, and compliance with regulatory standards. The role requires a Bachelor’s in a scientific discipline and 5+ years in a pharmaceutical lab, with strong documentation and teamwork skills.

Qualifications

  • Bachelor’s degree in a scientific discipline and 5+ years in a pharmaceutical lab, or equivalent.
  • Detail oriented and well organized; capable of multitasking.
  • Strong communication and teamwork skills; maintain confidentiality.
  • Ability to meet attendance standards and work 40 hours per week.
  • Experience with GMP, FDA/ICH guidelines, and regulatory inspections.

Responsibilities

  • Perform routine and non-routine microbiological testing (environmental monitoring, bioburden, microbial limits, endotoxin, sterility).
  • Review data for accuracy and GMP compliance; support CAPAs, deviations, and change controls.
  • Coordinate stability studies; manage sample inventory, schedules, and reports.
  • Prepare laboratory documentation, SOPs, protocols, and submission paperwork.
  • Assist with QC samples, including raw materials and finished drug products; monitor timelines.

Skills

GMP compliance
Microbiology techniques
Documentation
Regulatory audits
Stability testing
Environmental monitoring

Education

Bachelor's Degree in science

Tools

LIMS

Job description

Harrow, Inc. seeks a QC Microbiology professional to oversee routine and non-routine testing, data review, and stability program management in support of GMP manufacturing.

You will handle environmental monitoring, microbial testing, deviations, CAPAs, and compliance with regulatory standards. The role requires a Bachelor’s in a scientific discipline and 5+ years in a pharmaceutical lab, with strong documentation and teamwork skills.

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