Do you have expertise in Quality Assurance and a passion to play a critical role as the eyes and ears of our patients? If you have the passion and the drive to accelerate growth and make people’s lives better - then AstraZeneca is the place for you.
ABOUT ASTRAZENECA
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.
At AstraZeneca, we unlock the power of what science can do. Empowered to explore, everyday we work towards our ultimate aim – treating, preventing, modifying and even curing complex diseases.
BUSINESS AREA
In Quality, our work is important and valued. An unrivalled forward-looking mindset, there’s no better place to work at the forefront and learn how to add real value to a business throughout the lifecycle of our products – discovery, development and commercialisation.
As the voice of the patient, every batch we certify is a personal stamp of approval. Not something we take lightly, we are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes.
What you’ll do
Provides Quality Assurance support to an assigned area. Typically a graduate or equivalent experience. Non-supervisory, provides technical advice in key areas of processes and procedures. Role holder impacts directly on the value stream by ensuring efficient processes and procedures are maintained within the boundaries of regulatory compliance. For relevant GxP.
Typical Accountabilities:
Implement, monitor and update Quality Management System in accordance to AZ standard and local regulation
Monitoring the implementation and manage database of Quality & Compliance Manual
Manage and update complaint management
Manage training management
Review batch record and prepare the Certificate of Analysis before product disposition by Qualified Person
Prepare and update Site Master File
Prepare and update Master Formula
Manage all Quality Documentation including document control
Prepare Trending for Quality Performance
Essential for the role
Minimum hold bachelor’s degree of Pharmacy and having Apothecary degree
Having experience in Pharmaceutical company in QA or QC activities
Familiar with quality system and implementation of GMP
Good communication skill
Analytical skill and knowledge
Good in English, minimum passive
Computer literate
Why join Operations at AstraZeneca?
We are driven by our commitment to deliver accelerated growth for AstraZeneca and to make people’s lives better. It pushes us to keep building on our foundations and progressing as we turn our ever-growing and increasingly complex pipeline from molecule to medicine. Be part of evolving how we work with Lean, cutting-edge science, digitalisation and sustainable practices.
So, what’s next?
Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.
If you’re curious to know more then please reach out to Aziza Fitriani. We welcome your application, no later than August 22nd, 2021.
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram
If you have site, country or departmental social media then feel free to switch any of the above links.
Date Posted
23-Agt-2021Closing Date
29-Sep-2021AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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