Hobson Prior is seeking a QC Analyst to ensure quality control activities comply with Good Manufacturing Practice (GMP) standards. The successful candidate will support the production and release of gene therapy products and assist in the start-up of a new GMP facility.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Perform routine tests to ensure products are released on time.
- Support testing of raw materials and final products at external labs.
- Operate and maintain lab equipment, ensuring it is calibrated and ready for use.
- Record and investigate any deviations or non-conformances, and implement corrective actions.
- Help develop and update standard operating procedures (SOPs) and lab documents.
- Complete required training promptly to perform designated tasks.
- Maintain QC facilities to meet GMP standards and support site visits.
- Support the Quality Management System and ensure data integrity.
- Execute equipment qualification and method validation when needed.
- Propose and support continuous improvement programs.
- Ensure all work complies with GMP, Data Integrity, and Good Documentation Practice (GDP).
Key Skills and Requirements:
- Degree in a scientific discipline (e.g., Biochemistry, Chemistry).
- Familiarity with gene therapy and biologics methods (e.g., qPCR, HPLC, Western Blot).
- Experience with mammalian cell culture and/or flow cytometry is a plus.
- Strong problem-solving skills and ability to work well in group settings.
- Analytical skills to synthesize information and design workflows.
- Motivation to set and achieve challenging goals.
- Professionalism in handling pressure and interacting with others.
- Innovative thinking to improve work processes.
- Effective oral and written communication skills.
- Ability to occasionally lift items and work in a moderate noise environment.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Eagerness to learn and understand systems and processes.
- Ability to work in a fast-paced environment.
For more information, please contact Danielle Hull.
Apply now
If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.
Similar jobs
Negotiable
인천광역시, South Korea
Hobson Prior is working alongside a biotech company Technical Transfer Project Manager to join their team.
Negotiable
Shannon, Republic of Ireland
Hobson Prior is working alongside a biotechnology company to recruit for a dedicated QA Associate. This is a permanent position based in Shannon, Ireland.
Negotiable
Shannon, Republic of Ireland
Hobson Prior is working alongside a biotech seeking a QC Validation professional to join their growing teams. This is a 6-month contract role.
Negotiable
London, England
Hobson Prior is working alongside a pharmaceutical company seeking a Bioprocessing Team Leader Upstream to join their team.
Negotiable
Galway, Republic of Ireland
Hobson Prior is working alongside a client in Ireland to seek a Project Manager to join their team.
Can’t find what you’re looking for?
We don’t advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
Register