Quality Control (HPLC) (QMS)

Department: Quality Control (HPLC)

Designation: Officer to Executive

Experience: 2 to 5 Years

Education: M. Pharma, B. Pharma, M. Sc

Job Description:

To ensure that Good laboratory practices (GLP) is follow and maintain records of quality reports in the laboratory.

Demonstrate analytical activities and relevant documentation in quality control department.

Analysis of Finished Products / Raw material / in process & stability sample (Wet & instrumental analysis).

Calibration of HPLCs as per defined procedure and schedule.

Perform and Preparation of process Validation and hold time validation protocol.

Day to day handling of hurdles for smooth analytical work (Trouble shooting of instruments).

To ensure good documentation practices follow in the laboratory.

Co- ordinate with other department regarding issue.

To face regulatory and non-regulatory audits.

To ensure the labelling on regulatory and chemical in the QC Laboratory.

Participate in investigations of lab incident, OOS, OOT examine results, change control when necessary, generate deviation reports and root cause determination.

Department: Quality Control (QMS)

Designation: Sr. Officer to Executive

Experience: 3 to 6 Years

Education: M. Pharma, B. Pharma, M. Sc

Job responsibility

To ensure that Good laboratory practices (GLP) is follow and maintain records of quality reports in the laboratory.

Demonstrate analytical activities and relevant documentation in quality control department.

Statistical review of specification, STP, Protocol and other related documentation in quality control laboratory.

Develop and update SOPs related to GMP regulations.

Develop training and competency programs and trains the subordinates for error less results.

To ensure good documentation practices and follow in the laboratory.

Co- ordinate with other department regarding issue.

Responsibility to maintain Instrument Qualification (IQ, OQ, PQ) in the laboratory.

To ensure preventive maintenance and calibration of instruments. Communicate party for break down instrument.

To approve the COAs against raw data.

To ensure the labeling on regulatory and chemical in the QC laboratory.

To face regulatory and non-regulatory audits.

To ensure the product and material timely release.

Participate in investigations of lab incident, OOS, OOT examine results, change control when necessary, generate deviation reports and root cause determination and provide recommendations for corrective actions.

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URL: www.swiss.in

Contact Details :- 9737300746