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：
Routine Operations：
Overall manage, optimize, and review site quality systems, including but not limited to quality risk management, change control management, deviation management etc.In charge of build-up site quality manual, monthly quality management review and annually quality system review, to ensure the effectiveness of quality system meet with business requirements.In charge of participation and implementation of self-inspection, internal audit, and customer activities. Ensures that audits are performed per developed schedule. Review findings and makes recommendations for findings. Ensures timely response and closure of all action items / commitments.In charge of supplier quality management implementation which covers supplier/contractor audit, quality oversight of suppliers and contractors, quality & technical agreement with suppliers etc. And cooperate closely with global and peer site supplier management team to ensure the effective and efficient supplier management.Support on site quality KPIs and performance monitoring and Quality governance structure to maintain the process of management review and report the quality relevant metrics team with APAC quality.Ensure site quality system related documents aligned with ISO9001 standard and LSQ policy and procedure requirements.Responsible for facilitation of Annual Quality System Review activities such as risk register and Integration management review.Additional tasks assigned by line manager, as necessary.R&R on Compliance:
Strictly follow regulation\\SOP requirements, execute the operations with GMP common sense, fulfill Data Integrity requirements every time, all the time.Point out the activities or issues which is not compliance, report to manager in timely manner.
Who you are：
BS in Pharmaceutical, Science or equivalent.6+ years quality management experience in pharmaceutical, medical device, or life science industry.Excellent communication, problem-solving, planning and organization skillsFluent in English, both of written and oral.
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!