Senior / Principal Analyst, Quality Control

Posted 17 Days Ago
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Cambridge, MA
Senior level
Biotech
The Role
The Senior / Principal Analyst in Quality Control will lead method transfer and qualification activities, execute QC testing, manage testing programs, conduct investigations for root cause analysis, implement QC systems compliant with cGMP, and maintain compliance and inspection readiness in the QC unit.
Summary Generated by Built In

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

Top Skills

Elisa
Flow Cytometry
Mammalian Cell Culture
Qpcr
The Company
HQ: Cambridge, MA
97 Employees
On-site Workplace
Year Founded: 2015

What We Do

eGenesis is revolutionizing the field of transplantation with an unparalleled, multiplexed gene editing platform for the development of human-compatible organs, tissues and cells. Harnessing the latest gene-editing techniques, eGenesis has the capability to solve the global organ crisis by providing an alternative to allotransplantation.

eGenesis is uniquely positioned to reinvigorate the field of xenotransplantation by addressing both the key virology and immunology hurdles that have impeded its advancement to date and provide commercially-viable products to save and enhance the lives of patients in need.

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