Job Description

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.

Your role:
Fully support equipment selection, FAT, test and final acceptance in Solvent project. Avoid any equipment relative work delay affect the overall project progress.
Manage and ensure the Solvent equipment maintenance, qualification, periodical testing, etc. meet the acceptance ISO9001:2015. Avoid SOLVENT equipment failure cause the production interruption.
Ensure compliance of SOLVENT equipment with the requirement of the local government and company standard.
Visit and investigate the potential vendor and provide the conclusion of technical assessment in Solvent Project.
Actively participate in quality culture building and quality related activities
Actively report quality related events and participate in continuous quality improvement activities
Strictly comply with company EHS safety regulations and master skill of safety work and emergency rescue knowledge
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.
Take over the lead investigation for SOLVENT 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 of SOLVENT production interruption caused by maintenance & utility team.
Be responsible for installation and acceptance of new equipment to ensure the compliance with the requirement of the local government and company standard.
Ensure the good documentation practice, organize and manage technical drawings, manuals, documents. Keep drawings updated. Create, modify sops. To meet the requirements and ISO9001:2015.
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.
Analysis data (MTTR, MTBF, cost, labor-hour etc.) to improve PM and CM. Modify the process equipment to improve the equipment reliability and safety.

Who you are:
Bachelor or above degree in Mechanical engineering or related major.
At least 10 years production equipment maintenance/management experience with the pharmaceutical equipment or chemical process line.
Knowledge of occupational safety and basic GMP
Experience in non-standard equipment URS creation & FAT execution& Installation & Qualification.
Technical & Professional Knowledge:
English can read, write and speak fluently.
Strong coordination, analytical, judgment, communication and problem-solving skill.
Knowledge of GMP
High troubleshooting ability
Good customer focus and teamwork coordination

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety 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 a team that is dedicated to Sparking Discovery and Elevating Humanity!