Opening for Quality Control (AGM) at Unison
Pharmaceuticals
Quality Control - Assistant General Manager
B. Pharm/M.Sc./M. Pharm with 15 & above
years of hands-on experience of HPLC, GC, MLT, GLP, Dissolution apparatus and
UV Visible Spectrometer, for oral solid dosage forms.
Job Description:
- Monitoring of work allocation and previous day output review.
- Ensure current and relevant specifications, testing procedures and standard operating procedures are available in the laboratory to carry out the testing.
- To ensure required Reference standards, Columns, working standards, Microbiological media, etc. are available for testing.
- Release and Rejection of Raw materials, In process, Finished products and Packaging materials.
- Expertise in analyzed & handle finished products, in process samples, packing material, stability samples.
- Responsible for completion of activities such as OOS, OOT, SCAR, CAPA, Calibration and maintenance of all Q.C related instruments.
- Analytical support to all Process Validation activities, QC Documentation Control (Preparation, review & updating of QC SOPs ), standard testing procedure and specification.
- Knowledge of method development, impurity profiling, method validation technology transfer, validation, establishing specifications for new launch products.
- Competent in establishing QC lab as per cGMP/ cGLP requirement.
- Strong exposure in regulatory / customer audit expectations, audit compliance report and response to regulatory agencies queries.
- Co-ordination with internal customer departments, along with Lab support team which covers Calibrations of all QC instruments, Internal /External Audit & Compliance.
- Preparation & maintenance of working standards, Primary standards, Reference standards, Formation & Stability cell & handling of all stability study related activities, Instrument / Equipment Qualification activities.
Contact Person: Manisha Rajput
Interested candidates may also email their
resume to career@unisonpharmaceuticals.com
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