September 16, 2024
Job Type

Full-time

Description

Job Title: Quality Control Specialist I – HPLC
Location: Houston Headquarters’ Facility
Department: Quality Control & Analytic Development
Reports To: QC Scientist
FLSA Status: Full Time/Exempt

Mission Statement

The mission of Packgene Biotech is to accelerate gene therapy product development by providing an integrated one-stop solution including plasmid, viral vector, fill-finish and QC analytical services for the gene therapy industry.

Company Background

Packgene Biotech is founded in 2014 and headquartered in Guangzhou China. It provides CRO/CDMO services to the emerging gene therapy industry and research institutes. Packgene Biotech (US) is a full subsidiary of the parent company and is expanding its global footprint to Houston TX.

Overview

As our business grows quickly, we are looking for a qualified Quality Control Associate to undertake laboratory works under the guidance of senior scientists. The Quality Control Associate will have chance to learn a variety of molecular and cellular laboratory techniques, including cell culture, DNA extraction, solution preparation, etc.

General Responsibilities:

The Quality Control Specialist I  or II- HPLC will undertake laboratory work under the guidance of senior scientists. The Quality Control Specialist I or II is responsible to operate and maintain HPLC instruments; execute HPLC assays. The Quality Control Specialist I will have chance to learn Gene Therapy concepts and cGMP practice, etc

  • Conduct experiments under defined protocols under supervision of QC/AD scientist.
  • Routine lab activities may include
  • Prepare solutions, buffers, and reagents.
  • Execute analytical assays on HPLC instruments. Perform HPLC instruments maintenance.
  • Effectively plan lab activities by ensuring equipment readiness and reagents availability.
  • Order lab reagents and suppliers and monitor expiry of critical raw materials.
  • Maintain an accurate sample inventory.
  • Record all data and results following good documentation practices.
  • Collaborate closely with cross functional teams to ensure timely receipt and testing of samples.
  • Coach and train staff as needed.
  • Maintain clean working lab environment.
  • Revise, format documentation and study reports.
  • All other duties as assigned

Working conditions

In laboratory

Requirements

 

Qualifications

  • Bachelor’s Degree in Biological science or related field.
  • Experience working in a cellular or molecular biology laboratory is preferred.
  • Working knowledge of cell culture, AAV and experience with GxP-based laboratory setting and regulatory guidance is a plus.
  • Strong Interpersonal skills.
  • Strong problem-solving abilities and drive for success.
  • Excellent written and oral communication skills.
  • High level of self-motivation.
  • Keen attention to details.
  • Extensive experience working in a team-oriented, collaborative environment.

Physical Qualifications:

  • Mobility in facility.
  • Ability to lift up to 45lbs.
  • Visual and hearing abilities with or without correction.
  • Sitting and standing for extended periods of time.
  • All other duties as assigned.