Summary
Experience:
2 - 6 Years
Location:
Hyderabad / Secunderabad
Education:
UG - B.Pharma - PharmacyPG - M.Sc - Any Specialization
Industry Type:
Pharma/ Biotech/Clinical Research
Role:
QA/QC Exec.
Functional Area:
Production, Maintenance, Quality
Desired Candidate Profile
Responsible for In process quality assurance checks
In process Quality Assurance Checks & Sampling
In-process checks during manufacturing and packing process of Tablets, Capsules.
To give line clearance for the activity in production & dispensing activity.
Ensuring the periodic calibration of in process Instruments.
To inspect shop floor activities (self inspection) in compliance to SOPs and GMP.
In process Quality Assurance Checks & Sampling
In-process checks during manufacturing and packing process of Tablets, Capsules.
To give line clearance for the activity in production & dispensing activity.
Ensuring the periodic calibration of in process Instruments.
To inspect shop floor activities (self inspection) in compliance to SOPs and GMP.
Job Description
Responsible for In process quality assurance checks
In process Quality Assurance Checks & Sampling
In-process checks during manufacturing and packing process of Tablets, Capsules.
To give line clearance for the activity in production & dispensing activity.
Ensuring the periodic calibration of in process Instruments.
To inspect shop floor activities (self inspection) in compliance to SOPs and GMP.
To monitor the activities as well as status in shop floor as IPQA incharge.
Checking of all Equipment usage logbooks.
In-process documentation during dispensing and manufacturing
Review of Batch Processing Record
Review of Master documents like BMR, BPR, Validation Protocols
Shouold have an experience ranging between 2-5 yrs.
Should have good regulatory knowledge.
In process Quality Assurance Checks & Sampling
In-process checks during manufacturing and packing process of Tablets, Capsules.
To give line clearance for the activity in production & dispensing activity.
Ensuring the periodic calibration of in process Instruments.
To inspect shop floor activities (self inspection) in compliance to SOPs and GMP.
To monitor the activities as well as status in shop floor as IPQA incharge.
Checking of all Equipment usage logbooks.
In-process documentation during dispensing and manufacturing
Review of Batch Processing Record
Review of Master documents like BMR, BPR, Validation Protocols
Shouold have an experience ranging between 2-5 yrs.
Should have good regulatory knowledge.
Keywords: QA, IPQA, SOP
Company Profile
PharmaContact Details
Company Name:
Pharmaceutical Company
Website:
Not Mentioned
Executive Name:
Manju
Address:
Not Mentioned
Email Address:
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