Aizant Drug Research Solutions Pvt. Ltd Walk In Interview 2023 . Aizant Drug Research Solutions Pvt. Ltd Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.Aizant is an integrated drug development solutions provider. Aizant was established by experienced pharmaceutical professionals with global exposure.We are a rapidly growing formulation CDMO and CRO with a diverse portfolio of capabilities partnering with health care companies specializing in new molecular entities (NME’s).
Vacancy details:
- Post Name: Quality Control ( Formulation ) – GLP ( Assistant Manager )
- Qualification: B.Pharma in Any Specialization, B.Sc in Any Specialization/MS/M.Sc(Science) in Any Specialization, M.Pharma in Any Specialization
- Experienced:5 to 7 years
- Salary:Not Disclosed
Job Description: Greeting from Aizant Drug Research Solutions Pvt. Ltd
Important Details :
- Location: Hyderabad/Secunderabad
- Post of date:08/02/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Email:careers@aizant.com
Job description:
GLP monitoring and compliance in the lab.
Monitoring online documentation.
Preparation, review and approval of departmental SOPs.
Revision of SOPs as per regulatory/ Pharmacopeia updation.
Review and approval of technical documents/ protocols/ Report (Spec/ STP/ GTP/ RoA/ PV/CV/Stability/ AMT).
Impart laboratory trainings and scheduled trainings.
Train/ Evaluate/ qualify the analyst in the lab
Participate in laboratory investigations.
Ensure CAPA implementation.
Review of change controls.
Review of annual preventive maintenance calendar/ calibration/ qualification/ training calendars.
Participate in internal/ external audits and preparation of Audit response.
Ensure Qualification and maintenance of standards (WS, RS, IS etc).
Ensure calibration and preventive maintenance of laboratory instrument/ equipment.
Ensure proper Labeling of standards, chemicals and reagents and removal of expired materials.
Ensure that the HPLC / GC columns are used and maintained properly as per GLP.
Preparation and review of Record of analysis (ROA) for analysis.
Preparation, review and release of Certificate of Analysis (COA) for water samples, Raw materials and Packaging materials.
Analysis, review and release of Raw materials and Packaging materials.
Loading, withdrawal, testing, review and release of stability samples.
Ensure timely archival of the documents.
Qualification of Instruments/ Equipments.
Department resource planning and budgeting.
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