Followings will be the responsibilities of the position holder:
Compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity compliance.
Manufacturing and Packing process compliance in accordance with approved BMR/BPR.
To carry out line clearance, In-process checks at the different stages of batch manufacturing and packing.
Collection of control samples / stability samples / validation samples / other samples (as applicable) and maintain their record.
Issuance of Batch records and review of executed batch documents. Compliance of IPQA related SOPs and records.
Calibration of IPQA instruments and to maintain related records.
SOP training in ISO train of self-train within stipulated time.
To check and review the BMR/BPR, other related documents of finished goods.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email [email protected]
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