Qa Associate

Autolus Therapeutics; Stevenage; On-site; GBP 32,000 - 45,000; Full time

Job summary

Autolus is a biopharmaceutical company focused on next-generation T cell therapies for cancer and autoimmune diseases. The QA Operations team ensures GMP-compliant release and continuous improvement across sites in the UK, EU and US, centred at Stevenage.

The QA Associate will support batch release, QA documentation, and inspection readiness while working within a collaborative, fast-paced environment. A relevant BSc and GMP experience are preferred, with opportunities for growth and ongoing

Qualifications

• Higher education required.
• BSc in pharmaceutical services, immunology, biology, chemistry or relevant discipline.
• Experience with GMP systems and controlled documentation.
• Ability to work in a cleanroom environment.

Responsibilities

• Maintain GMP compliance in a multi-product facility.
• Assist in batch release related activities and report issues.
• Manage quality documentation and audit trails.
• Review batch manufacturing and quality control records for issues.
• Prepare and check in-process and drug product labels in line with templates.
• Support in generation of departmental metrics and archiving of records.
• Assist preparedness for inspections and adherence to safety policies.

Skills

Good communication

Attention to detail

Accurate data entry

Workload prioritisation

Reliability

Team player

Multi-tasking

Education

BSc in pharmaceutical services

BSc in immunology

BSc in biology

BSc in chemistry

Job description

Work with us
Our team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.

Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working environment which actively promotes creativity, leadership and teamwork – together we are ONE Autolus.

Job Description

Job Title: QA Associate

Reports to: QA Manager / Senior QA Specialist

Department: Quality Assurance – QA Operations

Hours: Full Time (shift based), Sunday – Wednesday 08:00 – 17:45

Location: Stevenage

About Autolus

Autolus is a biopharmaceutical company, advancing innovative therapies at both clinical and commercial stages of development, focused on next-generation, programmed T cell therapies for the treatment of cancer. Using a broad suite of proprietary and modular T cell programming technologies, the company is engineering precisely targeted, controlled, and highly active T cell therapies designed to better recognize cancer cells, break down their defence mechanisms, and eliminate these cells. Autolus has a pipeline of product candidates in development for the treatment of haematological malignancies, solid tumours, and autoimmune diseases.

Why Autolus

Our team is passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy to deliver life-changing treatments to patients. Whilst working at Autolus you will enjoy a flexible, diverse, and dynamic working environment which actively promotes creativity, leadership and teamwork. In addition to this Autolus is proud to offer a competitive salary, performance related bonus as well as private medical insurance, life assurance, pension and access to an employee share scheme. Autolus promotes flexible working.

Our Promise

Autolus is developing complex, breakthrough therapies for a globally diverse market and equally recognises that diversity amongst our people is critical to our mission. As we draw on our differences, what we’ve experienced, and how we work, we celebrate diversity and are committed to creating an inclusive environment for all employees

Role Summary

Based in Stevenage, the post-holder will work within the Quality Assurance team, supporting the delivery of autologous CAR T-cell products for commercial purposes and clinical trials operating in sites across the UK, EU and US from a central Good Manufacturing (GMP) site in Stevenage (UK). You will be expected to work with a team of quality professionals to provide a high-quality service to external service users.

Key Responsibilities

• Maintaining the requirements of Good Manufacturing Practice in a multi-product facility delivering cell and gene therapies for clinical trial and commercial purposes.
• Interact with various functions to ensure cGMP compliance in batch release related activities. Report or escalat to Line Manager any issues.
• Control of record forms for use in production and QC, applying batch or test article identity traceability features and maintaining an audit trail of issue, use and reconciliation.
• Review of Batch Manufacturing Records and Quality Control records and escalation of quality issues
• Preparation and checking of in-process and Drug Product labels, ensuring compliance with the authorised template and the batch-specific/patient-specific data thus maintaining product traceability and regulatory compliance.
• Identify potential compliance risks/gaps and recommend improvements.
• Under supervision, review of premises and equipment documentation including; logbooks, protocols, reports and equipment maintenance forms.
• To liaise with internal departments regarding quality issues when required.
• Under supervision, supports in the generation of departmental metrics.
• Conduct the archiving of documentation and records within the QA team.
• Support inspection readiness activities.
• Work in adherence to local Health and Safety policies and SOPs.
• To perform other duties which are directed by the line manager/QA Team Lead.
• Any other duties as required following consultation with the post holder.
• Contribute to the continuous improvement of the Pharmaceutical Quality System (PQS).
• Contribute and facilitate in quality event investigations and in the determination of root cause.

Demonstrated skills and competencies

E – Essential

P – Preferred

Experience

• Experience working with GMP systems and controlled documentation (P).
• Meet requirements to work in cleanroom environment (P).

Qualifications

• Higher education (P)
• BSc in pharmaceutical services, immunology, biology, chemistry or relevant discipline (P)

Skills/Specialist knowledge

The post holder will bring expertise related to:

• Good communications skills
• Good eye for detail
• Accurate data entry skills
• Good workload prioritisation skills, decision-making and scheduling skills
• Reliability, flexibility, motivation and a responsible team-orientated attitude
• Ability to manage multiple activities to tight deadlines

Autolus Core Competencies

• Focus on Results: Works to meet business goals set by management and leaders
• Builds Trust and Relationships: Ensures trust with internal and external partners by delivering on commitments
• Resilience: Has the capacity to recover quickly from difficulties; toughness
• Communicates and Collaborates: Builds partnerships and works collaboratively with others to meet objectives

Autolus is committed to the protection of the personal information that we collect & process and we are fully compliant with General Data Protection Regulations (GDPR).

Autolus is committed to providing an inclusive and fair workplace for all. We are an equal opportunity employer and do not discriminate on the basis of race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic. We also provide reasonable accommodations throughout the recruitment process.

Autolus’ success is driven by equality and inclusion; we believe all voices are of equal value and must be heard. Whilst operating with focus and integrity, we are committed to improving diversity and inclusion within our business and our industry.