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Senior / Principal Analyst, Quality Control

COMPANY MISSION

At eGenesis, we aspire to deliver safe and effective human transplantable cells, tissue and organs utilizing the latest advancements in genome editing. 


POSITION SUMMARY

eGenesis is seeking a Senior / Principal Analyst to join the Quality Control unit. You will be responsible for method transfer, qualification, troubleshooting, and release and stability testing of our innovative drug substance and products. You will ensure activities are executed in a cGMP compliant manner and play a pivotal role in the build-out of our internal Quality Control function as eGenesis expands clinical capabilities. The ideal candidate will be highly motivated, excited by technical challenges, and work well in a team environment.


PRIMARY RESPONSIBILITIES
  • Lead method transfer and qualification activities in support of our pre-clinical and clinical programs
  • Execute QC testing to support release and stability analysis for drug substance and drug product
  • Manage method qualification and release testing conducted at contract testing organizations
  • Conduct testing investigations and deviations to support root cause analysis and corrective and preventative actions, as required
  • Implement QC systems and procedures compliant with cGMP
  • Manage programs for critical laboratory reagents, assay controls/reference standard, and equipment
  • Independently analyze and summarize data in technical reports and presentations
  • Author, review, and/or approve data, logbooks, SOPs, CoAs, analytical methods, protocols, reports, deviations, and other quality records
  • Maintain the QC Unit in a state of compliance and inspection readiness


BASIC QUALIFICATIONS
  • BS/MS in biology, immunology, biochemistry or a related scientific discipline with at least 5-8 years industry experience
  • Experience working in a regulated GMP QC laboratory is required
  • Proficient in a range of analytical methods (mammalian cell culture, flow cytometry, ELISA, qPCR etc.) and aseptic technique
  • Strong knowledge of US cGMP regulations/guidelines
  • Detail oriented and organized with the ability to work in a fast-paced environment
  • Effective communication skills, both verbal and written, across various functions including Manufacturing, Quality Assurance, and Analytical Development


Average salary estimate

$100000 / YEARLY (est.)
min
max
$80000K
$120000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

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MATCH
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FUNDING
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
No info
LOCATION
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EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
February 8, 2025

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