Technical Services Supervisor (Cikarang Site)
Job Summary
Technical Services Supervisor
Do you have expertise in and passion in the pharmaceutical manufacturing industry Would you like to apply your expertise to impact the lives of patients in a company that follows the science and turns ideas into life changing medicines Then AstraZeneca might be the one 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 worlds most serious diseases. But were more than one of the worlds leading pharmaceutical companies. We are on a journey to bring life-saving medicines to patients. Our role in contributing to decreasing mortality rates globally is clear shaping the future by spotting a scientifically-led commercial opportunity and acting now to operationalise and scale it.
ABOUT OPERATIONS CIKARANG
Located at Cikarang (West Java) our production site is equipped with modern infrastructure and staffed by an inclusive network of diverse and high performing teams. The site upholds stringent quality standards and fosters innovation. Prioritizing a science-led approach Safety Health environmental sustainability and collaboration are key priorities in our way of work. We are committed to delivering safe and effective pharmaceutical solutions to improve patient outcomes in Indonesia.
BUSINESS AREA
Join the team where everyone feels a personal connection to the people that we impact. From our science labs to manufacturing at scale we are committed to delivering at the highest quality. Its inspiring and rewarding work influencing every part of the product lifecycle to deliver life-changing medicines. To ultimately make peoples lives better from patients and their families to all of us in society. Take advantage of the huge opportunities to drive efficiencies in our processes and produce better-quality outputs. Now is the time to join and make a bigger impact as we commit and accelerate our growth in Lean.
What youll do
Face exciting new challenges with the support of others to navigate our constantly changing manufacturing environment. We never give up in diligently ensuring our patients receive quality and safe medicines responding to a large variety of often complex demands.
Site Digital Champion:
Site Champion for AsiaPac Digital Network
Lead and support business function (Production Engineering Logistic and Quality) to deliver Site Lean Digital Initiative target
Liaise with Regional and Global Digital Support to ensure the right support to enable Site delivered all Lean Digital target is provided
Provide
Validation & Qualification (excludes: AMV & Cleaning Validation):
Support system owner in preparing internal validation & qualification protocol for process & equipment
Support execution of internal validation protocol and prepare validation report in coordination with the system owner
Review external validation & qualification protocol and report in coordination with the system owner
Computerized System Validation (CSV)
Support system owner in protocol for Computerized System Validation
Support execution of CSV in liaise with system owner and Campus IT support
Review external validation & qualification protocol and report related with CSV in coordination with the system owner and Campus IT and/or IT QM support function
Maintain adequate knowledge of operating systems and application software used to provide a high level of support for system owner for any changes and/or modification required revalidation.
Ensure compliance to AZ policies.
Ensure assigned trainings are attempted and completed as per agreed timeline.
Ensure compliance to GMP procedures when working with IT systems in GMP areas.
Maintains and consistently demonstrates a general knowledge of company guidelines processes practices and procedures.
Essential for the role
A bachelors degree in Information Technology (IT). Candidates with Industrial Engineering background with high passion for digitalization are welcome to apply.
Relevant experiences/knowledge on implementing digital applications such as Power BI Power Apps Manufacturing Execution System (Tulip would be an advantage).
Experience in working with wide networking environment with minimum supervision.
Familiar with GMP and SHE (Safety Health and Environment) standard.
Excellent communication skill.
Analytical skill and knowledge.
Proficient in English.
Desirable for the role
Has experience in pharmaceutical industry
Has good knowledge in project management.
Has knowledge in design applications (i.e. Corel draw Adobe Photoshop)
Proficient in GMP standard and regulatory requirements.
Experience in project management will be an advantage.
Why AstraZeneca
Here youll have the opportunity to make a meaningful difference to patients lives. With science at its heart this is the place where breakthroughs born in the lab become transformative medicines for the worlds most complex diseases. Answer unmet medical needs by pioneering the next wave of science focusing on outcomes and shaping the patient ecosystem.
With our ground-breaking pipeline the outlook is bright. Be proud to be part of a place that has achieved so much yet is still moving forward. Theres no better time to join our global growing enterprise as we lead the way for healthcare and society.
So whats next
If youre curious to know more please reach out to Aziza Fitriani (). We cant wait to hear from you.
Where can I find out more
Follow AstraZeneca on LinkedIn: AstraZeneca on Facebook: AstraZeneca on Instagram: 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.
Date Posted
01-Sep-2026Closing Date
29-Sep-2026AstraZeneca 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.
Required Experience:
Manager
About Company
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more