Teva Global Open Innovation Senior Analyst 

Israel, Center District 

767106894

• Responsible for ensuring the Teva Larne Engineering Systems, Procedures, Documentation, Facilities and Equipment are maintained and fully functional
• Plan, direct and coordinates activities concerned with design, construction, modification, and maintenance of equipment and machinery in industrial plant
• Establishes standards and policies for pollution control, installation, modification, quality control, testing, operating procedure, inspection, and maintenance of equipment, according to engineering principles and safety regulations
• Directs maintenance of plant, buildings and equipment and coordinates requirements for new designs, surveys, and maintenance schedules
• Tests newly installed machines and equipment to ensure fulfilment of contract specifications
• Undertake any other duties, which may be assigned by Senior Management
• Create and organise new preventive maintenance / calibration / non- routine maintenance and review existing records on computerised asset management system e.g. breakdowns / non-routine
• Organise preventive maintenance / calibration internally including external contractor(s)
• Maintain / monitor site Building Management System
• Procurement of additional plant / Equipment. This includes creating / reviewing qualification documentation and sourcing plant / equipment from relevant suppliers
• Create / review risk assessments for engineering and general site health and safety
• Supports Site Health and Safety committee, provide advice and carry out duties attached to this role. Carryout Health and safety inspections and Audits for the Teva Larne Site and create / review risk assessments for engineering and general site health and safety
• Create / review / maintain engineering SOPs
• Raise any corrective and preventive actions (CAPAs) / Change Controls (CCRs) / Deviations (DRs) as and when required. Liaise with relevant departments about site / equipment issues to ensure cGMP compliance
• Proactively implement safe systems of work. Be responsible for the protection and safety of other company personnel and minimising environmental impacts
• Upkeep documentation necessary for compliance with FDA, MHRA and external and internal audits

Are you….

• Educated to HNC level or above would be preferred

Do you have?

• Significant practical experience of working within an engineering based role in a highly regulated manufacturing environment
• GMP environment expereince
• Practical knowledge of the following techniques:
  • Project Management Experience
  • Health & safety Experience
  • Fault Finding Experience
• Demonstrable IT Skills e.g. Microsoft Office
• Strong communication skills
• Proven ability to maintain high standards of work, attention to detail and right first time approach
• Self-motivated with the ability to work largely unsupervised
• The ability to work proactively and under time constraints
• Team working and interpersonal skills
• A flexible approach to changing priorities and able to adjust working hours as necessary including participation in an on-call rota

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Deadline for internal applications will close on Wednesday 23rd July2025