Site Engineer
- Location:
- Liverpool jobs
,
Merseyside jobs
- Salary:
- £28000 - £34000 per annum
- Company:
- RHL.
- Job type:
- Permanent jobs
- Date posted:
- 05/11/2009 15:39
- Job id:
- 45869657
- Contact:
- Nigel Billinge
- Ref:
- Totaljobs/0911-30
Site Engineer
Job Purpose
As a member of the Engineering Department the successful candidate will be required to perform a wide range of activities associated with the scheduled and unscheduled maintenance and/or calibration of equipment.
Job Summary
Engineers will be required to perform all assigned activities in accordance with regulatory requirements and company engineering, safety and quality systems.
Initially reporting directly to the Engineering and Validation Director, the Site Engineer will perform both the day to day routine requirements, scheduled and unscheduled PPM (planned preventative maintenance) tasks as well as more varied project dependant tasks.
Key Responsibilities
Carry out planned and unplanned preventative maintenance on all site equipment in accordance with regulatory guidelines and company procedures.
Ensuring all associated documentation is completed fully in real time in accordance with company procedures.
Systems such as HVAC with HEPA filtration, steam boilers, LTHW boilers, compressed air systems and multiple water systems are maintained as per their validated status, thus ensuring compliance with all quality procedures and regulations.
Continuously strive to improve equipment operation and offer solutions for best practice.
To participate in activities relating to corrective and preventative actions, change control and investigation of deviations.
Achieve compliance with all company and site SOP?s, written schemes of examination and production plans by forward planning for all tasks.
Maintain a safe working environment by continuously promoting safety awareness, recognising and rectifying unsafe conditions and completing thorough investigations and reports when incidents occur.
To understand and comply with HS&E rules and regulations with regards to the site.
To communicate and co-operate with other departments such as Production, Process Development, Quality Control and Quality Assurance.
Manage sub-contractors where appropriate
To participate in the writing and review of Standard Operation Procedures data collection sheets.
On call out of hours roster duties.
Provide detailed reports on works completed and parts used to Supervisor.
To train on equipment, techniques and procedures as required.
To take responsibility for the maintenance and expansion of a personal training record.
To participate in regulatory and client inspections as required.
To participate in special projects and validation activities as required.
Experience
Hands-on experience within a cGMP biopharmaceutical or pharmaceutical environment.
Ideally a range of experience with different clean room utility or biopharmaceutical manufacturing equipment.
Skills, Knowledge and Personal Attributes
