Your mission
As a QC Analyst, you will be responsible for ensuring continued Good Manufacturing Practice (GMP)-compliant activities within QC to support the manufacture and release of plasmid and gene therapy products.
This role will be a part of aiding the start-up of a new GMP facility for the production of gene therapy products. As such, it will involve participating in equipment qualification, method transfer and routine in-process and release testing within the QC labs, in addition to other QC-supporting activities.
Job Description
- Execute routine analytical testing to support timely release of product.
- Support testing at external contract labs for raw materials and final product.
- Operation and maintenance of laboratory equipment ensuring all equipment is calibrated and suitable for use in alignment with test schedule.
- Record Out-of-Specification, non-conformances, investigations and implementation of corrective action(s) where applicable.
- Assistance with the development and updating of SOPs and laboratory documentation.
- Ensure all training is undertaken in a timely manner as required to perform activities designated.
- Maintain QC facilities to meet GMP requirements, conduct necessary checks to support any health authority, customer/stakeholder site visits.
- Support with maintaining the Quality Management System and controlling of documents and assuring the data integrity of all data produced.
- Execution of equipment qualification and method validation/transfer when required.
- Propose and/or support the development and implementation of continuous improvement programs.
- Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures.
- Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken.
- Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions are closed timely and in a RFT state.
Job Experience
- BSc in a scientific discipline e.g. Biochemistry, Chemistry.
- Minimum 0-2 years’ experience working in a GMP environment.
- Experience in working with gene therapy and/or biologics methods e.g. qPCR, HPLC, Western Blot, SDS-PAGE, DNA extraction, Spectrophotometry.
- Experience with mammalian cell culture and/or flow cytometry preferred.
- Proficiency in Microsoft Office software preferred, specifically Word, Excel and PowerPoint.
- Wants to learn and have a natural curiosity to understand systems and processes.
- Ability to work in a fast-paced environment essential.
Why us?