QA Validation Specialist

We currently have an opportunity for 3x QA Specialists to join Autolus' growing QA Team, with roles split across our QA Validation and QA Supplier Management Teams. The roles will see you supporting the delivery of autologous CAR T-cell production in compliance with Good Manufacutring (GMP). The role is based from our Stevenage site (hybrid working between...

**Location**: - Stevenage**Job Summary**: We currently have an opportunity for 3x QA Specialists to join Autolus' growing QA Team, with roles split across our QA Validation and QA Supplier Management Teams. The roles will see you supporting the delivery of autologous CAR T-cell production in compliance with Good Manufacutring (GMP). The role is based from...

**Location**: - Stevenage**Job Summary**: We currently have an opportunity for a QA Specialist to join Autolus' growing QA team, working within their QA Compliance team. We are recruiting this role to increase the compliance support to our cell manufacturing operations outside of core hours. As such the role will be a shift based role, with the days worked...

**Bring more to life.** Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you...

**Location**: - StevenageThe (Senior) Clinical Quality Assurance Specialist is responsible for quality oversight activities within Clinical development by supporting and managing cross-functional relationships with business process owners and external stakeholders. Maintains Quality Assurance oversight in Clinical Operations and Clinical Development. This...

**Role Summary** Qualification and validation of manufacturing systems capable of producing high quality drug products for use in Autolus clinical trial and later commercial programs. The role is based within the Autolus Manufacturing sites, Stevenage, but may involve travel to other sites in London such as White City. They will perform qualification and...

**Employer description**: Primenet UK are a Managed Services Provider and trusted IT solutions company. They offer a range of trusted IT services, from support to security to maintenance — well known for their customer service as well as their IT services. **Overview:** You will have the opportunity to gain valuable skills, knowledge and experience as...

Job Title: QA Specialist - Document Controller Job Type: 6 Months Industry: Pharmaceuticals Location: Stevenage Salary: £18-£20 per hour Start Date: ASAP To provide management of the Veeva Quality Docs (VQD) system, the core GxP Documentation System used on site. Key Activities Provide role of VQD Process owner, including acting as superuser and local...

The post holder will work in the Product Delivery Quality Assurance team, supporting the delivery of autologous CAR T-cell products for clinical trials operating in sites across the UK and EU from a central Good Manufacturing (GMP) site in Stevenage (UK) and headquarters in White City, London. Please note this role is working Monday to Friday, 9am to 5pm...

**Role Summary** Qualification and validation of manufacturing systems capable of producing high quality drug products for use in Autolus clinical trial and later commercial programs. The role is based within the Autolus Manufacturing sites, Stevenage, but may involve travel to other sites in London such as White City. They will perform qualification and...