We apologize your item could not be found. Not all items are listed on our website. Please contact your account manager for details regarding your searched item.
Material number (eg: xxxxxxxxxxx) no space or hyphen needed.
No Results Found
Your Password has changed! Please login again
Cart
Outdated Browser Detected
Our website has detected that you are using an outdated browser that will prevent you from accessing certain features.
Please use one of the below recommended browsers to improve your browsing experience
Team Member Spotlight: Rusli Kartadinata, Associate Quality Manager, Asia Pacific
Here at West, we are working by the side of our patients and customers to help contribute to a healthier world. Meet one of our team members, Rusli Kartadinata, and read his story to learn how he grew in his career at West from a Production Engineer to his current role as the Associate Quality Manager across Asia Pacific.
Tell us about your current role at West
I currently work as a Regional Quality Associate Manager in Asia Pacific. I support regional quality projects, technology transfers as well as China DMF (Drug Master File) submissions with two members on my team.
Can you share some background on your career path at West to date?
I’ve experienced an interesting nine years at West. I joined West in 2011 as a Production Engineer in the Operations department, where I was responsible for the Finishing and Metal production area, and then moved to the molding and trimming production area as a Senior Production Engineer. In 2017, I moved to Quality and took the role of Associate Quality Control Manager, where I was able to develop different skills such as Lean Six Sigma and ISO 9001 auditor. West provided me many useful training courses such as Leading Others, Leadership and People Management to help me grow from an individual contributor to a manager. Most recently, I have been promoted to my current role, Associate Quality Manager, supporting our Asia Pacific region.
What drives you to keep pursuing more opportunities, and do you feel well supported by West in your pursuit?
I’m a firm believer in a lifelong journey of learning. Thanks to the variety of roles I’ve held, as well as opportunities such as projects, mentoring and training courses given by West, I’ve enjoyed fruitful growth for my career and will keep working hard and continuously learning.
What do you like most about working for West?
West is a global company with people coming from different backgrounds, enabling me to have a different perspective on daily work, and providing the opportunity to learn more about different cultures across the world.
When you think about our mission to improve patient lives around the world, how do you think you help accomplish that mission within your role?
As One West Team, we come together to deliver for our customers and help them address their challenges. Most importantly, when we work as a team, everyone has the same mindset to achieve the best outcome, and most importantly, to improve patients’ lives.
To learn more about working at West, visit our Careers page.
The coring and fragmentation of elastomer components used in containment of parenteral drug products continues to be a challenge. Many factors influence these phenomena, so it is critical that a pharmaceutical manufacturer understands how a vial system will be used, for example: what is the recommended needle gauge, is it single- or multi-dose, could spikes, vial adapters or closed system transfer devices be used. Cores and fragments can be generated by needle penetration of the elastomer components. Cores are formed by the needle cannula cutting the elastomer – ordinarily they are cylindrical. Fragments are formed via an abrasion phenomenon of the needle penetration – shapes are irregular. <br />
West’s turns 100 today! A milestone that we are very proud of, and something few companies have the opportunity to celebrate. In honor of our 100th anniversary we are spotlighting our former President, Bill West, son of our founder Herman O. West.
Part 1 of this two part blog series, gave a high-level overview of the new ICH guideline <em>Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management</em>. In part 2 of this blog series, some of the key takeaways will be discussed in more detail. <em>Q12</em> is intended to help companies demonstrate increased product and process knowledge, and understand which post-approval changes will require a regulatory submission, as well as the level of reporting for each category.
West has been busy behind the scenes building our offerings in the West Knowledge Center. The Knowledge Center launched just over a year ago, and since then we’ve more than doubled our content based on customer requests and real-time data and analytics.
We know that performance, as well as sustainability, are equally important to our customers. For West, we are demonstrating our efforts in critical areas such as carbon neutrality, recycling and reuse of products, and secondary packaging. In addition to our own efforts, we collaborate with our customers and suppliers to solve these challenges, including alignment of Environment, Social, and Governance goals, and efficiency in operation.