Similar posts
QC Scientist
- Permanent
- Good Clinical Practice (GCP)
- United Kingdom
This vacancy has now expired. Please see similar roles below...
We are seeking a bright, enthusiastic and motivated QC (Quality Control) Scientist, ideally with experience in the a GCLP (good clinical laboratory practice) environment to join a growing multi-disciplinary team and support the development of a next generation personalised cancer medicines. The role is based in Stevenage and is a great opportunity to play an active role in transforming the management of cancer.
Job Responsibilities
- Carrying out QC testing of raw materials, in process controls, and finished product, in line with GMP regulations.
- To assist in the preparation and review of documentation including SOPs and risk assessments to ensure the highest levels of controls and traceability.
- Perform immune monitoring for clinical trials and ensure all activities are undertaken in accordance with GCLP and quality standards.
- Assist in the design and validation of immune monitoring assays using flow cytometry and ELISpot.
- Perform maintenance and calibration of laboratory equipment including flow cytometers.
- To coordinate activities with manufacturing to ensure appropriate and timely sampling and testing of raw materials, in-process samples and finished product.
- Be accountable to the Principal QC Scientist.
Skills and Requirements
- MSC in a Biological Science discipline.
- 3 years' experience in a scientific laboratory role.
- Experience working in a GLP/GCLP regulated environment.
- Experience in human cell isolation, and cell and tissue culture.
- Experience in flow cytometry and ELISpot.
- Experience in assay validation.
- Understanding of GCLP guidelines.
- Strongly focused on quality and safety.
- Have excellent planning and organisational and time management skills.
- Have good communication and interpersonal skills.
- Self-motivated with strong initiative and drive.
To Apply
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Dominic Cappell on 02039671074 or upload your CV on our website - www.proclinical.com/send-cv
A full job description is available on request.
#LI-DC1
#Quality
Related jobs
Highly Competitive Salary
Rochester, USA
Proclinical is seeking a proactive and dedicated individual for a Customer Quality Specialist for a leading pharmaceutical company. This is a permanent position located in Rochester, NY
Highly Competitive Salary
Zebulon, USA
Proclinical Staffing is seeking a QC Chemist to join an ambitious pharmaceutical company.
Highly Competitive Salary
Marietta, USA
Proclinical Staffing is seeking a QC Laboratory Technician to join a cutting-edge biopharmaceutical company.
Highly Competitive Salary
Raritan, USA
Proclinical Staffing is seeking a QC Investigation Specialist (Level 1, 2, 3, & Senior) to join a global biotech company.
Highly Competitive Salary
Cambridge, USA
Proclinical is seeking a QA Specialist - Equipment and Computer Systems to join a global biopharmaceutical company.
Up to US$44 per hour + Highly Competitive Salary
Philadelphia, USA
Proclinical Staffing is seeking a Quality Control Analyst: Cell Therapy to join a cutting-edge biotech company.
US$100000 - US$115000 per annum + Highly Competitive Salary
Philadelphia, USA
Proclinical is seeking a QC Microbiology Supervisor for a leading biotechnology company.
Highly Competitive
London, England
Proclinical is seeking an Associate Director, GCP Quality to contribute to the mission of developing better medicines, faster to work remotely.
US$200000 - US$230000 per annum
San Francisco, USA
Proclinical are recruiting for a Director, Clinical QA (GCP) to join a biotech organisation. This role is on a permanent basis and is located in the Bay Area.