Engineering Scheduling Team Lead

Job description:

Do you pride yourself on your integrity? We do what’s right for our employees, patients and partners so can you?

 

We are recruiting for an Engineering Scheduling Team Lead to manage the Engineering Scheduling Team’s activities and associated support functions, including all equipment scheduling for the laboratories and manufacturing shutdowns including planned maintenance and reactive repairs, calibration.

 

Oxford Biomedica’s Engineering team are responsible for all aspects of Plant, Mechanical, Electrical, and Incoming utilities at our facilities.

 

Your responsibilities in this role would be:

 

• Manage and oversight of the Engineering Administrators workloads and priorities to ensure that the scheduling functions operates seamlessly with the business requirements.
• Ensure that Equipment scheduling activities are recorded correctly to allow a comprehensive record of the equipment history to be maintained.
• Management of computerised maintenance management system (CMMS) and supporting procedures.
• Management of maintenance contracts, supporting vendor selection, contractual negotiations, tender process alongside procurement.
• The managing, developing, coaching, and mentoring of Engineering administrators.
• Lead root cause analysis investigations to resolve complex and technical problems, implementing suitable and sustainable solutions.
• Lead asset maintenance and calibration interactions with Health Safety & Environment (SHE), customer and regulatory auditors.

 

 

We are looking for:

 

• Good standard of secondary education with preferably A level or equivalent in English, Maths and Science
• A considerable excellent working knowledge of the preventative maintenance process in a GMP environment
• Experience of managing assets within a regulated engineering or GMP manufacturing environments
• Significant experience working within an Enterprise Resource Planning system (ERP) and or Computerised Maintenance Management System (CMMS)
• Experience of interpreting technical documentation & problem solving.
• Proven ability to manage a team or sub function inclusive of people management.
• The ability to build cross departmental relationships to support the objective of the function.
• Microsoft Office expertise within MS Word & Excel, Outlook & MS Teams.
• A good understanding of Health and safety practices and contractor permit management.

 

 

 

About Us:

 

We are a quality and innovation-led cell and gene therapy CDMO with a mission to enable our clients to deliver life changing therapies to patients around the world.  Our innovative solutions and proven expertise allow our clients in the biotech and biopharma industry, to deliver life-saving therapies to reach even more patients.  The success of cell and gene therapy products transforms outcomes for millions of people suffering from some of the world’s worst diseases and medical conditions.

 

What’s in it for you:

 

• Highly competitive reward packages.
• Wellbeing programmes.
• Development opportunities.
• A 35-hour working week.
• Welcoming, friendly, supportive colleagues
• A diverse and inclusive working environment.
• Our values are: Deliver Innovation, Be Inspiring and Have Integrity.
• 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.

Profile description:

We are looking for:

 

• Good standard of secondary education with preferably A level or equivalent in English, Maths and Science
• A considerable excellent working knowledge of the preventative maintenance process in a GMP environment
• Experience of managing assets within a regulated engineering or GMP manufacturing environments
• Significant experience working within an Enterprise Resource Planning system (ERP) and or Computerised Maintenance Management System (CMMS)
• Experience of interpreting technical documentation & problem solving.
• Proven ability to manage a team or sub function inclusive of people management.
• The ability to build cross departmental relationships to support the objective of the function.
• Microsoft Office expertise within MS Word & Excel, Outlook & MS Teams.
• A good understanding of Health and safety practices and contractor permit management.

 

 

 

About Us:

 

We are a quality and innovation-led cell and gene therapy CDMO with a mission to enable our clients to deliver life changing therapies to patients around the world.  Our innovative solutions and proven expertise allow our clients in the biotech and biopharma industry, to deliver life-saving therapies to reach even more patients.  The success of cell and gene therapy products transforms outcomes for millions of people suffering from some of the world’s worst diseases and medical conditions.

 

What’s in it for you:

 

• Highly competitive reward packages.
• Wellbeing programmes.
• Development opportunities.
• A 35-hour working week.
• Welcoming, friendly, supportive colleagues
• A diverse and inclusive working environment.
• Our values are: Deliver Innovation, Be Inspiring and Have Integrity.
• 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.

We offer:

Oxford Biomedica is a quality and innovation-led viral vector CDMO that enables its clients to deliver life-changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, Oxford Biomedica has more than 25 years of experience in viral vectors, the driving force behind the majority of gene therapies.  

 

Cell and gene therapy is the treatment of disease by the delivery of therapeutic genetic material (DNA or RNA), into a patient’s cells. One highly effective approach to delivering genetic information is to re-engineer existing viruses to be safe delivery vehicles (vectors) to insert the genetic material into patients’ cells. This can be achieved either by directly administering the vector to the patient (often referred to as in vivo gene therapy), or by first introducing the genetic material to cells or tissue outside of the body, before administering the cells or tissue into the patient (often referred to as ex vivo gene therapy or gene-modified cell therapy).  

 

Oxford Biomedica 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. Oxford Biomedica'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.