Similar posts
GMP Biotechnologist
- Permanent
- Good Manufacturing Practice (GMP)
- United Kingdom
This vacancy has now expired. Please see similar roles below...
An international biotechnology company is recruiting a GMP Biotechnologist to their UK office. The organisation focuses on gene therapy to treat the suffering of people suffering from chronic systemic diseases. With a next-generation gene therapy platform to provide treatments for a wide range of diseases, this position represents an exciting opportunity to work with a leading company.
Job Responsibilities:
- Be part of the GMP manufacturing operations team responsible for delivering GMP manufacturing batches for clinical studies.
- Become fully trained in all areas of the manufacturing process as required and responsible for practical delivery of key process steps.
- Write SOPs and batch records to support GMP manufacture.
- To work closely with Catapult warehouse team, Freeline-QC, and Catapult Scheduler to perform the effective transfer of materials/samples/waste into and out of the grade C cleanroom as required by the daily manufacturing plan and daily BOM.
- Ability to identify issues as they occur and report accordingly with all relevant information.
- To support GMP Operations in deviations, investigations and change controls as required.
- Team member involved in practical delivery of technology transfer of new processes into GMP Operations according to approved protocols.
- General duties involved in the maintenance of clean room production facilities to GMP standards and preparation for manufacture.
- To be trained in USP/DSP equipment SOPs as required for supporting GMP batch manufacture.
Skills and Requirements:
- Educated to degree level or equivalent in a biological science.
- 1-2 years of hands-on, practical experience in GMP manufacture of biopharmaceuticals.
- A sound understanding of the required industry standards for GMP manufacturing of investigational medicinal products.
- Hands on experience in the upstream and/or downstream processing for biopharmaceuticals.
- Experience of working in GMP.
- Experience of mammalian cell culture techniques.
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
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 Joshua Godden at + 442038540101 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
Proclinical Staffing is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#LI-JG1
#Compliance/Quality
Related jobs
US$25 - US$30 per hour
Norton, USA
Proclinical is on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.
Highly Competitive
Visp, Schweiz
Proclinical is seeking a QC Analyst to join our client's team in Switzerland.
Highly Competitive
Solothurn, Switzerland
Proclinical is seeking an Associate Quality Control professional to join our client's team in Switzerland.
Highly Competitive
Basel-Stadt, Schweiz
Are you passionate about quality and precision? Join our client as a dedicated Quality Manager and help ensure top-tier standards every day.
Highly Competitive
Visp, Switzerland
Proclinical is seeking a QC Associate to join the Bioanalytics Microbial Team at our client's facility.
US$0.00 - US$25 per hour + Highly Competitive Salary
Fremont, USA
Proclinical is seeking a Maintenance Technician to ensure the smooth operation of facility systems and equipment.
Highly Competitive
King of Prussia, USA
Are you passionate about quality and precision? Join our client as a GMP Cleaning Associate and help ensure top-tier standards every day.
Highly Competitive
Paris, France
Proclinical is seeking a dedicated professional to join our client's team as a Device Regulatory Documentation & Compliance Senior Manager.