Unison Pharmaceutical opening for Quality control apply now
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.
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
Interested candidates may also email their resume to career@unisonpharmaceuticals.com