Quality Sepcialist

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.  

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

• Assist to set up and maintain operation quality document system, guide and monitor document execution, make sure NTLC meets the requirement of GSP and Merck standard.
• Responsible for products inspection and release, be strictly follow with the standards, methods and sampling principles stipulated by GSP, inspect the products purchased and sold return etc. and complete inspection and acceptance record in time.
• Responsible for quality operation monitoring, guide and supervise the quality management during processes like purchase, storage, maintenance, sales, rejection, transportation, etc.
• Responsible for warehousing quality monitor, including periodic onsite quality check, communications with LSP, quality KPI monitor etc.
• Support the investigation, handling and report of quality incident (deviation).
• Responsible for non-conforming products confirmation and process supervision.
• Product Returns: assessment of product returns and supporting information to verify if products are suitable for return to saleable status or destruction.
• Organize and coordinate validation and calibration related activities, to ensure completion in time and compliance with regulatory and Merck requirements.
• Organize and coordinate the training of business operation.
• Support the internal and external audits.
• Support supplier and distributor qualification and audit.
• Responsible for quality management and quality guarantee capability of the carrier authorized for transportation.
• Monitor T&T system implementation
• Responsible for local quality index data collection and follow-up, report to management team as required.
• To recognize a reportable Adverse Event (AE) or Safety Information and ensure the information is forwarded to the Local Patient Safety Person (LPS) in Merck, Inc. within 24 hours.
• Keep well relationship with stakeholders.
• Backup for the other quality members.

• Bachelor's degree or above in pharmacy, biology, chemistry, medicine, or other related areas
• Licensed Pharmacist. is preferred
• Good English skill at reading, writing, listening, and speaking
• Above 3 years' quality experience in GMP or GDP (GSP) area is preferred
• Good communication skills in both scientific and non-scientific information
• Professional knowledge in GSP, GMP and GDP
• Problem solving ability and skills
• Ability to face challenges and self-learning
• Teamwork

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!