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Posté 25 mai 2023
Wuxi, Jiangsu - China
Demander un identifiant 264658
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
Lead and maintain the equipment maintenance, qualification, periodical testing, etc. meet the acceptance of GMP and standard. Avoid equipment failure caused the production interruption.
Ensure compliance of process equipment with the requirement of the local government and standard
Maintenance troubleshooting capability on all plant machines
MTTR, MTBF data analysis to reduce shutdown time
Support new equipment, upgrade and renovation projects
Able to support the SAT/IOQ, and drive for problem solving.
Ensure the behavior in accordance with compliance and EHS, complete the training on time.
Perform routine equipment safety inspection and machinery optimization during daily site survey.
Recommends technical solutions for improving EHS and realize the recommendations after approval into a technical solution.
Support the accident/incident reporting and investigation.
Take over the lead investigation for process equipment deviations and CAPAs
Support the Qualification / Validation activity including start-up for new or maintained equipment/new products
Check and manage to ensure no production interruption caused by maintenance team.
Be responsible for installation and acceptance of new equipment to ensure the compliance with the requirement of the local government and Merck standard.
Ensure the good documentation practice, tidy up and manage the technical drawings, manual, documents, change management, keep the updated drawings and create, revise SOPs to comply with GMP requirement.
Spare parts control with the daily requisition issue and budget including the local manufacture to replace the imported spare parts partly.
According to the production plan of production department, make maintenance plan, estimate working hours and contact production team to arrange personnel.
Communicate with production team to make sure equipment and facility meet their requirements.
Analysis data (MTTR, MTBF, cost, labor-hour etc.) to improve PM and CM. Modify the process equipment to improve the equipment reliability and safety.
Pursue for the optimization of equipment function and continue improvement for equipment and system.
Other works assigned by department head.
Who you are:
Bachelor or above degree in Mechanical engineering or related major.
3-5 years production equipment maintenance/management experience with the pharmaceutical equipment or Biopharmaceutical process line.
Knowledge of occupational safety and GMP
PE bag making industry experience is plus.
Technical & Professional Knowledge:
Knowledge of GMP
High troubleshooting ability
Good customer focus and teamwork coordination
Experienced user of Office software as well as data bases
Functional Area: Engineering & Skilled Trade
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!