A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
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.
This role aim to lead and oversee the day-to-day and end-to-end activities in our research and development function, Site Pharma Technology (SPT). While the role give you the opportunity to ensure the effectiveness of the team as well as cost-efficiency of the ongoing projects, you will showcase your ability in configuring best solutions and deliver ground breaking innovation as well as collaborate cross-functionally to aim the best products for patients and customers.
Responsibilities:
Lead the development and validation of analytical method for developed product/raw material as well as get involved in the selection of external lab.
Lead and supervise day-to-day of qualification projects, e.g. formulation, lab trial, pilot scale trial, stability monitoring, etc.
Manage all quality testing of product development until commercial production stage, e.g. maintenance, non-routine testing, transfer project, etc.
Oversee the documentation in SPTs lab, GMP-GLP compliance, as well as SMLK3 implementation.
Identify and develop all quality document related to Analytical and Galenical Development activities.
Responsible to the cost effectiveness of lab activities or projects.
Who You Are:
Minimum 3-4 years working experience in Analytical Development in Pharma Industry.
Having 1 year experience in Coordinator role/managing team is preferrable
Proven experience in Analytical Development projects.
Good understanding in laboratory instruments.
Strong in data analysis and problem solving
Fluent in English both written and verbal (able to conduct presentation in English)
Strong leadership and excellent task-management
Self-motivated, strong work ethics and good interpersonal communication.
Willing to work on-site
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. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!
Curious? Chat with one of our curious minds on our interactive Q&A platform and catch a glimpse of our people, values, and culture. You can also apply and find more information at https://jobs.vibrantm.com
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.merckgroup.com/en/company/press-positions.html
Job Requisition ID: 251675
Location: Jakarta Timur
Career Level: C - Professional (1-3 years)
Working time model: full-time
North America Disclosure The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at
844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request. You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.
Notice on Fraudulent Job Offers Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information .
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