To maintain analytical records as per GLP requirements and timely review all analytical data.
Plan Stability sample for analysis and maintained daily work allocation.
Management of stability chamber
Co-ordination with the other department / other locations wherever necessary.
To issue the analytical work record for analysis.
Ensure timely completion of training of team before allocation of work and Create awareness
about critical steps.
Ensure availability of current specification and testing procedure.
Review Analytical data, cleaning method validation protocol and reports
Review and ensure availability, traceability and reconciliation chemicals and standards.
Review the certificate of analysis.
Ensure solution preparation, labelling and contemporaneous documentation.
Ensure proper consumption of Standards, logs, labelling and all relevant entries are done online.
Review electronic, non-electronic data and audit trails.
Preparation of Qualification, validation protocols, standard operating procedures.
Initiate procurement process for consumables as per requirement.
Responsible for investigation of Incident, Out of calibration ,Out of specification, Out of trends,
Laboratory incidence and deviation in laboratory and work on continuous improvement area for
Ensure management of HPLC/GC Columns.
To handle the QMS documents in the laboratory.
Salary: INR 7,00,000 - 8,50,000 PA.
Industry: Pharma / Biotech / Clinical Research
Employment Type: Full Time, Permanent
Desired Candidate Profile
Education:UG -B.Sc - Any Specialization, Chemistry
PG - MS/M.Sc(Science) - Chemistry, Any Specialization
his campus has multi product Tablet and Capsule manufacturing facilities.
It has a State-of-the-Art Pilot plant for manufacturing Exhibit batches for Regulated Markets. This facility has been successfully inspected by UKMHRA, W.H.O, NDA-Uganda & PPB- Kenya. The products manufactured are exported to Europe, CIS, Asia-Pacific and African countries.