Unison Pharmaceuticals hiring B.sc, M.Sc, B.Pharm, M.Pharm for QC - GLP

 Unison Pharmaceuticals hiring B.sc, M.sc, B.pharm, M.pharm for QC - GLP

Unison Pharmaceuticals Pvt Ltd Recruitment 2021. Unison Pharmaceuticals Pvt Ltd Notification full detailes below.Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and most affordable medicines across the nation.

Important Vacancy details:

I. Post Name: Quality Control – GLP

II. Education: B.Pharm, B.Sc, M.Sc, M.Pharm

III. Experienced:02 to 6 years

IV. Location: Ahmedabad( Moraiya ), gujarat

V. Address: Unison Pharmaceuticals Pvt. Ltd. Unit – II, B– 6, Steel Town, Opp. CIL Nova Petro, Behind HOF, Moraiya, Taluka : Sanand, Ahmedabad – 38 22 13.

Note:If Intrested Candiadtes Send Updated Resume Below Email id. career@unisonpharmaceuticals.com

Job Description: We have requirement for the post of Quality Control – GLP in Unison Pharmaceuticals Pvt Ltd ! If Intrested Candiadtes Send Updated Resume Below Email id.

career@unisonpharmaceuticals.com

Opening for Quality Control – GLP

Roles and Responsibility

 Responsible for handling of instruments like HPLC, Dissolution Test Apparatus, UV Spectro Photometer, Disintegration Apparatus and Other Physico Chemical instruments.

 Responsible for perform the Calibration of all Analytical Instruments/Equipment lying at Quality control laboratory.

 Responsible to perform Equipment/ Instruments Calibration/ Verification. In-case of OOC results inform to superior immediately and follow respective SOP.

 Responsible for maintain the Inventory, log record of HPLC columns as per respective Column management SOP.

 Execution of Calibration and Preventive Maintenance of QC instruments as per predefined schedule.

 Working Standard, Reference Standard and Chemical/Reagent management.

 When require give the support in Analytical document preparation like SOPs , Specification, Method of Analysis , Worksheet , Analytical Method Transfer Protocol and Report.

 To follow Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Safety precautions during routine analytical activities.

 Daily/ weekly monitoring of Temperature/ Humidity of QC laboratory.  To ensure availability of current version SOPs, Specifications, MOAs, STPs.

 To prepare SOPs, Specifications, MOAs, STPs and other documents.  Responsible for preparation of Analytical documents like Specification, Method of Analysis and Worksheet for Active Raw Material, Inactive Raw Material, Finished Product, Finished Product Strip/blister, Semi Finished Product, Granules, and Packing Material and for working standard qualification.

 Preparation and maintenance of Miscellaneous documentation.  Archival and Retrieval of Quality documents.

For all the positions, candidates should also have sound knowledge cGMP documentation and must be familiar with cGMP requirements

Interested candidates may also email their resume to career@unisonpharmaceuticals.com

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