Negotiable
Undetermined
Remote
Remote
Summary: The Equipment Engineer role involves planning and executing engineering assignments related to life cycle management initiatives, focusing on commissioning, qualification, and decommissioning of equipment. The position requires documentation of instrument calibration, technical protocol writing, and coordination with cross-functional teams. Candidates must have experience in the consumer, OTC, or pharmaceutical industry, with a strong emphasis on cGMP practices. Proficiency in MS Office and technical documentation is also essential.
Key Responsibilities:
- Plan and execute equipment engineering assignments for life cycle management initiatives.
- Engage in commissioning, qualification, and decommissioning activities.
- Document and maintain instrument calibration records.
- Determine appropriate commissioning and decommissioning activities for equipment.
- Write technical protocols (URS, FRS, SAT, FAT) and reports for equipment qualifications and line clearances.
- Lead and coordinate activities with cross-functional teams.
- Update equipment layouts and ensure drawings are revised for line clearance.
- Ensure equipment is updated or removed from the system as necessary.
- Experience with Lock out and Tag out procedures.
- Utilize MS Office for technical documentation.
- Demonstrate good written and verbal communication and presentation skills.
- Work with cGMP documentation and practices.
Key Skills:
- Commissioning and Qualification experience.
- Experience in the Consumer, OTC, or pharmaceutical industry.
- GMP experience.
- Proficiency in MS Office.
- Technical documentation skills.
- Strong communication and presentation skills.
- cGMP working experience.
Salary (Rate): £30 hourly
City: undetermined
Country: undetermined
Working Arrangements: remote
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Job Description:
>> Plan and execute equipment engineering assignments concerned with large life cycle management initiatives.
>> Engage in the commissioning and qualification of the equipments and line clearances and decommissioning activities.
>> Ensure instrument calibration are documented and up to date.
>> Determine the appropriate Commissioning decommissioning activities for the equipmentsystem being commissioned decommissioned.
>> Write technical protocols (URS,FRS,SAT,FAT) and reports for equipment qualifications, line clearance, equipment removals.
>> Lead and Co-ordinate activities with cross functional teams.
>> Red line equipment layout and ensure drawings updates are made for line clearance. (mechanical, electrical, utility drawings etc.)
>> Ensure equipments are updated in system or removed from the system.
>> Plus to have the experience in Lock out and Tag out procedures practices.
>> MS Office expertise, Technical Documentation.
>> Good written & verbal communication, presentation skills.
>> cGMP (Current Good Manufacturing Practice) working experience. cGMP documentation proficiency.
Requirements:
>> Commissioning & Qualification experience.
>> Specific experience within the Consumer, OTC, or pharmaceutical industry is must.
>> GMP experience