Responsible to ensure the implementations of GxP in the product manufacturing activities by means of inspection in alignment with BI’s safety, quality and compliance target and policy.
Duties & Responsibilities:
Performing inspections and making timely decision on non-critical quality incidents (e.g : defect after QC release or non-conformity, defect after delivery, release or stop production process) in Production/Warehouse/Technical area to ensure cGMP compliance implementation.
Manage retained sample of finished product
S1 Pharmacist or equivalent
1 - 2 years in pharmaceutical industry, experience in manufacturing process or quality will be an advantage.
In depth knowledge of current Good Manufacturing Practice (cGMP)
Willing to work in shift schedule
Who we are:
At Boehringer Ingelheim we create value through innovation with one clear goal: to improve the lives of patients. We develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long term performance. We are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture. Learning and development for all employees is key, because your growth is our growth. Want to learn more? Visit boehringer-ingelheim.com and join us in our effort to make more health.
If you have any question on the recruiting process, please contact:
[email protected][email protected] Note to Recruitment Agencies:Boehringer Ingelheim (BI) does not accept candidate submissions from recruitment agencies that BI does not have existing contracts with.BI will not be responsible for payment of recruitment fees for the hiring of candidates whose resumes were submitted to BI employees or BI offices without BI’s prior permission.
Job - Quality/Compliance
Primary Location - Africa, Asia, Australasia-Indonesia
Organization - ID-PT Boehringer Ingelheim Indonesia
Schedule - Full-time
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