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von: Quotient | localité: EysinsN: Quotient
The role is a full-time, permanent position, based in Eysins, Switzerland.
JOB PURPOSE
You will be part of the team that validates and maintains microarrays manufacturing system. You will follow, update and create procedures to maintain the MosaiQ™ manufacture microarrays handling existing and new production equipment. Manufacturing is in compliance with agreed specifications for the manufacture of high-quality diagnostic reagent consumables according to GMP. As a result, you will maintain equipment in accordance with agreed procedures, supporting and ensuring manufacturing operates to achieve planned quality and output targets. You will also actively participate in the creation and review in updating of procedures, SOP’s and any other relevant documents. As a first line technical support, you will implement continuous improvements to increase reliability and productivity of the production line.
JOB RESPONSILITIES
Ensure the daily business.
- Support manufacturing operates to achieve planned quality and output targets.
- Become trained to operate manufacturing equipment.
- Become trained to perform internal maintenance/calibration following SOP’s.
- Intervene in case of equipment breakdowns.
- Track all failures within active trackers.
- Report to and advise line manager on operational activities.
Ensure the Maintenance & Calibration activities.
- Ensure assets are registered on the quality system and up to date.
- Manage Preventive Maintenance & Calibration plans on equipment.
- Pilot and monitor Maintenance & Calibration indicators.
- Maintain and Calibrate equipment, in accordance with agreed procedures, ensuring equipment is operating correctly per qualified process.
- Maintain accurate and legible records to ensure relevant laboratory documentation is kept in a satisfactory condition.
- Check, control and maintain work environments according to the requirements of GMP and relevant Health and Safety policies contributing to the maintenance of agreed standards.
Master training and become a technical expert on equipment and processes.
- Actively participate in the review / update of procedures, and any other relevant documents.
- Participate in continuous training and assessment, in accordance with personal development plan.
- Maintain excellent levels of cleanliness and housekeeping.
- GMP guidelines and Quotient standard operating procedures are always adhered to.
- Participate to new processes or equipment implementation.
- Within an agreed area/process or equipment, implement and/or collaborate on any continuous improvements.
QUALIFICATIONS & EXPERIENCE REQUIRED
- Diploma in Electromechanics or Automation
- 3-5 years of experience in a similar role within a GMP production environment, ideally in a classified ISO8/7 clean room and/or medical device or pharma environment.
- Ability to interface with custom automated production equipment.
- Strong problem-solving skills
- Ability to work independently and work in a team.
- Ensure good communication to give efficient manufacturing processes within the team and across the organization.
- This is a weekly rotating shift position scheduled according to the business needs between 6:00am and 10:00pm
