Taron Solutions Limited Taron Solutions Limited is a contract development and manufacturing company (CDMO) for biopharmaceuticals which provide innovative processes and proprietary know-how for fast and reliable process development and scale-up production that will meet GMP requirements and one-stop...

Taron Solutions Limited

 

Taron Solutions Limited is a contract development and manufacturing company (CDMO) for biopharmaceuticals which provide innovative processes and proprietary know-how for fast and reliable process development and scale-up production that will meet GMP requirements and one-stop solution from early cell development, protein modification, optimization, formulation, to GMP manufacturing.

Method Development and Validation Specialist

Job level Middle
Work exp Minimum 5 Years
Education Bachelor Degree
Location
Within Hong Kong
Industry Biotechnology / Chemicals / Testing / Laboratory
Job function Science / Lab / Research > Biotechnology
Published On 09/11/2019
ref. TS-QC003

Summary

Taron Solutions Limited is entering an exciting period to build our global brand servicing pharma and biopharma industries. We are looking for a Quality Control Professional at our Hong Kong Headquarters to join our project in developing and setting up our Quality Control Laboratory for our sterile manufacturing facility. The individual conducts duties and responsibilities listed below, plus any other tasks as requested by the supervisor.

 

Duties and Responsibilities

  • Conduct test method development for protein and cell testing for R&D project.
  • Prepare test method validation protocol, report and subsequent test procedure.
  • Prepare related QC equipment qualification documents.
  • Conduct QC equipment qualification and calibration and supervise supplier and contractor for related maintenance activities.
  • Perform any ad hoc works assigned by supervisor.
  • Assist in the equipment purchasing and sourcing consumables required for QC testing.
  • Identifies and interprets data independently. Performs data management and tasks to record results effectively in lab notebook or computer system with minimal supervision.
  • Provide training and technology transfer for test method developed.

 

Requirements:

  • Holders of a bachelor's degree in a relevant science subject, such as biological science, biotechnology and molecular technology, life science, biomedical science, cell biology, biochemistry, accredited chemistry, tissue engineering, cell and molecular biology, etc.
  • At least 5 years of working experiences, with a minimum of 3 years relevant working experiences in method development and validation.
  • Working experience or research experience in advance therapeutic product is a plus.
  • Independent and a good team player.
  • Good troubleshooting skills.
  • Good understanding in international standard such as GMP, ISO or other QMS standard.

 

Salary will be based on educational level, discipline, and years of experience. Other benefits based on short-term and long-term incentive performance base (cash and stock options)

Candidates interested in applying for this position can send a cover letter as well as an updated CV with contact information to the following .