Manufacturing Training Officer - #141772

We are currently recruiting for two roles: Training Officer and Senior Training Officer to join the Manufacturing and MSAT department.

The purpose of this roles is to provide support to GMP manufacturing by ensuring the training activities for new and existing employees within the department are coordinated and fully implemented to meet the regulatory requirements.

Our manufacturing team is a critical part of OXB’s operations. We produce multiple clinical and commercial lentiviral vector-based gene therapy products and manufacture the adeno-based vaccines.

Your responsibilities in this role would be:

• Delivering induction sessions of new employees within the Manufacturing and MSAT department, such as classroom presentations and practical training in the clean room.
• Delivering various training sessions to the departmental staff as required, in the office environment and in the clean room facilities.
• Scheduling and performing operator’s initial qualifications and requalification’s required for GMP manufacturing in timely manner.
• Performing reviews of documentation such as qualifications protocols and following up the sign offs of documentation to ensure qualifications are finalized in timely manner.
• Supporting departmental managers in keeping the staff training records up to date with all relevant documentation and evidence required to prove competencies of the staff.
• Organisation of resources and materials to be used during training activities.
• Providing support for creating and improving training materials.
• Monitoring departmental training trackers and supporting completion of necessary activities to meet training requirements.
• Delivering key metrics and trends to reflect the current training status of the teams in the department.
• Acting as the Subject Matter Expert (SME) for training and aseptic procedures in the Manufacturing team.
• Completing QMS records within the Manufacturing department. This includes DEV, DI, CAPA, CC’s and EME’s/EMEI’s.
• Traveling between OXB sites as required.
  
  

We are looking for:

• Proven experience performing training sessions for individuals and groups.
• Experience in performing clean room qualifications such as gowning and aseptic would be an advantage.
• Strong knowledge of Microsoft Office applications such as Excel, Word and PowerPoint.
• Knowledge of GMP production, documentation requirements and regulatory standards would be desirable.
• Excellent verbal and written communication skills.
• Ability to schedule multiple activities and prioritise.
  
  

About Us:

OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies.

OXB collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus (AAV) and adenoviral vectors. OXB’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.

What’s in it for you:

• Highly competitive total reward packages
• Wellbeing programmes
• Development opportunities
• Welcoming, friendly, supportive colleagues
• A diverse and inclusive working environment
• Our values are: Responsible, Responsive, Resilient, Respect
• State of the art laboratory and manufacturing facilities
  
  

We want you to feel inspired every day. We’re future-focused and our business is growing rapidly. We succeed together through passion, commitment and teamwork, and so can you.

Collaborate. Contribute. Change lives