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.
<br />In 2016, the China Federal Drug Administration (CFDA) made two announcements regarding packaging of parenteral drug products. Per these announcements, stability studies of packaging materials should refer to protection, compatibility, safety and functionality properties.
The rise in type 2 diabetes has sparked a variety of treatment options, including glucagon-like peptide-1 (GLP-1) receptor agonists. GLP-1s are a class of injected drugs (additional oral options are currently in development) that “mimic the action of GLP-1 and increase the incretin effect in patients with type 2 diabetes, stimulating the release of insulin.”<sup>1</sup> Commonly used when oral treatment alone is not enough, the benefits of GLP-1s include a reduction of glucagon and glycosylated haemoglobin (HbA1c), weight loss and a low risk of hypoglycemia.<sup>2</sup>
<p>In <a href="/blog/2017/june/corporate-responsibility-for-2016">Part 1</a> of this blog series, we highlighted the Compliance and Ethics section of West’s inaugural Corporate Responsibility Report. </p><p>In Part 2, we will cover West’s commitment to serving the communities in which we live and work.</p>
In a product’s development lifecycle, the importance of packaging can sometimes be overlooked until a packaging specialist becomes involved and can elucidate whether the packaging design is suitable and meets the tests for form, fit and function. Some companies that may not understand or emphasize the critical elements of a good package in the design phase may find out too late that the package is unsuitable after sustaining one or more failures during validation testing.
Critical quality attributes (CQAs) of biologic drug products can be affected by multiple factors throughout the product lifecycle, including the container closure and delivery systems. Diane Paskiet, Director of Scientific Affairs at West Pharmaceutical Services, discussed containment and delivery system compatibility with biologic drug products along with regulatory considerations in her presentation Establishing Safety of Container Closure and Delivery Device Systems at the PepTalk 2017 conference. Evaluating potential impacts early, holistically, and throughout bioprocessing can facilitate decisions at each step that will minimize risks to CQAs and safety.