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Join us in shaping the new era of cell and gene therapies

How to apply:
Please email your CV and cover letter to [email protected]

Assistant Production Manager
Posted On: 2022.01.24
Job Description

  • Manage GMP facility site and routine operation of production lines and warehouse to ensure compliance with GMP standards.
  • Prepare, implement and maintaining production document including SOP & Batch Production Records to comply with regulations, standards and requirement from company, government authorities and customers.
  • Participate the planning and implementation of policy and procedures in the areas of product quality, manufacturing strategies, manpower and cost control.
  • Solving practical problems and initiating continuous improvement in manufacturing.
  • Conducting staff training and team supporting for GMP knowledge.
  • Maintain and monitor the maintenance and calibration for machines/ equipment/ tools.
  • To perform cleanroom cleaning according to SOP and GMP procedures.
  • To assist the head of production to monitor the production workflow.
  • To assist monitor the production process according to the production plan.
  • Perform qualification and validation activities (e.g process validation, cleaning validation) by preparation of protocols and reports.
  • To participate in Pharmaceutical Quality System (PQS) activities including change control, deviation investigation, CAPA and quality risk assessment.

    • To perform the daily operation and ad-hoc functions of the Production Department.

Qualification and Requirements

  • A holder of a bachelor’s degree or above in Manufacturing, Life Science
  • discipline such as biotechnology, biochemistry and medical laboratory or related
  • discipline with at least 5 years of GMP experience.
  • Preferably with knowledge and/or experience in cell culture and/or GMP
  • manufacturing of pharmaceutical, biological and cell products.
  • Hardworking, initiative, self-motivated and attentive to details.
  • Able to work under pressure and willing to work overtime.
  • Good communication, problem-solving, time management and prioritization skills
  • Proficiency in English and Chinese, and computer skills.
Production Officer / Assistant Production Officer
Posted On: 2022.02.22
Job Description

  • Assist the Production Manager in developing, implementing and maintaining the documentation system, including the equipment maintenance record.
  • Ensure and maintain adequate and accurate records for controlling and monitoring conformity to specified GMP and statutory requirements.
  • Assist in monitoring the calibration & maintenance program of production equipment and facility.
  • Ensure qualification and validation activities are performed as per prescribed schedules.
  • Handles deviation, performs investigation and corrective actions and preventive actions (CAPA).
  • To perform the daily operation and ad-hoc functions of the Production Department.
Qualification and Requirements

  • A holder of a bachelor’s degree in Life Science discipline such as biotechnology, biochemistry, chemistry and medical laboratory science. Candidates with less experience will be considered for the Assistant position. Fresh graduates in the related field may also be considered.
  • Preferably with knowledge and experience in GMP manufacturing of pharmaceutical, biological and cell products.
  • Hardworking, initiative, self-motivated and attentive to details. Able to work under pressure and a team player.
  • Good communication, problem-solving, time management and prioritization skills.
  • Proficiency in English and Chinese, and computer skills.
QC Research Assistant / Associate (Molecular & Biochemistry)
Posted On: 2022.02.16
Job Description

  • Performing test method validation experiments.
  • Preparation of QC test Standard Operating Procedures (SOPs).
  • Performing QC tests on advanced therapeutic products and publish test reports.
  • To communicate, arrange and keep track of outsourced contract laboratories activities.
  • Preparation and execution of equipment / instrument Qualification as assigned by Management.
  • Raise Change controls and Assist in Deviations/investigations/Quality risk management and CAPA for quality related activities.
  • Proactively suggest and raise concerns to ensure GMP practices are followed.
  • Implement the actions as necessary through proper management follow up.
  • Other ad hoc tasks as assigned by supervisors and management.
Qualification and Requirements

  • Research Assistant: Bachelor’s degree in biotechnology, biological sciences, biomedical engineering, life sciences or other related disciplines with 0-2 year relevant experience.
  • Research Associate: Master’s degree in biotechnology, biological sciences, biomedical engineering, life sciences or other related disciplines with at least 2 years relevant experience.
  • Laboratory experience with tissue culture/ molecular biology / toxicity assays /qPCR / chromogenic assays.
  • Proven ability to work productively in GMP environment is a plus.
  • Strong inter-personal skills, attention to details and a team player with self motivation.
  • Excellent prioritization skills, time management and problem solving skills.
  • Proficiency in English and Chinese, and computer skills such as Office, Zoom/Teams etc.
  • Possess the drive to succeed and to participate in the growth of an exciting, fast-paced company.
Production Supervisor

Job Description:

  • Developing, implementing and maintaining the documentation system, including the Standard Operating Procedures (SOPs) & Batch Production Records.
  • To perform cell culturing, cleanroom cleaning according to SOP and GMP procedures.
  • To assist monitor the production process according to the production plan.
  • Perform qualification, validation and Pharmaceutical Quality System (PQS) activities.
  • Handle deviation, performs investigation and corrective actions and preventive actions (CAPA).
  • To perform the daily operation and ad-hoc functions of the Production Department.

Qualification and requirements:

  • A holder of a bachelor’s degree or above in Life Science discipline preferable with Immunology, Biochemistry or Medical Laboratory science, with at least 3 years of laboratory experience.
  • Preferably with knowledge and experience in cell culture and/of GMP manufacturing of pharmaceutical, biological and cell products.
  • Hardworking, initiative, self-motivated and attentive to details.
  • Able to work under pressure.
  • Good communication, problem-solving, time management and prioritization skills.
  • Proficiency in English and Chinese, and computer skills.
Lab Officer (QC Analytical Team)

Job Description:

  • Research into and perform molecular, biological and biochemical tests in the field of Advanced Therapy Products (ATP), such as flow cytometry, cell viability, qPCR, mycoplasma test
  • Perform test method validation according to industry best practice and international guidelines.
  • Participate in test method development and transfer.
  • Be a team member of the Quality Control (QC) Department, and support laboratory daily operations.
  • Other duties as assigned by the supervisor or management team.

Qualification and requirements:

  • Holder of Bachelor’s degree in biotechnology, biochemistry, biology,  life science and other related disciplines.
  • Minimum 1 year’s work experience in Life Science industry, preferably in Immunology or Cell Biology field. 
  • Interested to join the cell and gene therapy manufacturing and testing industry.
  • Strong inter-personal skills, attention to details and a team player with self motivation.
  • Excellent communication, problem solving, time management and prioritization skills.
  • Proficiency in English and Chinese, and computer skills such as Office, Zoom/Teams etc.
  • Possess the drive to succeed and to participate in the growth of an exciting, fast-paced company.