Executive Quality Control Abbott Healthcare

3.0 - 10.0 years

0 Lacs

Baddi, Himachal Pradesh, India

On-site

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JOB DESCRIPTION: Job Description Designation : Executive/Sr. Executive Qualification : M.Sc. or Equivalent Reports to : Manager QC Experience Required: 3 to 10 yrs Having adequate knowledge of Sampling, Testing of Raw material, Packing Material, Finish Product, Validation and Stability samples. Having adequate knowledge of Laboratory Instruments and equipment's Calibration, Maintenance/External calibration. Having adequate knowledge of Preparation of laboratory chemicals, Reagents, test solution, and Volumetric solution. Having adequate knowledge of Reference, Chemical and Working standard management i.e., Working Standard qualification and support in working standard management. Having adequate knowledge of Data entry in SAP. Having adequate knowledge of operation and trouble shoot of HPLC/UV/IR and other QC analytical instruments and its software. Having adequate knowledge of data entry management in inventory/Information management software of QC like LIMS software. Having adequate knowledge of preparation of the QC documents like SOPs, Protocols and general documentation. Having adequate knowledge of Pharma Industry Guidelines and Pharmacopoeias. Having exposure of regulatory audit and GDP/DI compliance. Having adequate knowledge of GLP / GMP requirements. The base pay for this position is N/A In specific locations, the pay range may vary from the range posted. JOB FAMILY: Operations Quality DIVISION: EPD Established Pharma LOCATION: India Village Mauza : Baddi ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Not specified MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

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Junior Research Associate- ADL NDDS (R&D) Bharat Serums and Vaccines

1 - 3 years

3 - 4 Lacs

Navi Mumbai

Work from Office

Role & responsibilities Operation & calibration of Instruments in Laboratory. Analysis & report compilation of In-process samples, Stability samples, Finished products & Raw materials. Preparation of chemicals & reagents required for day-to-day analysis. Preparation & filtration of Mobile phase Preparation & standardization of volumetric solutions Stock checking & inventory of chemicals required for day to day Stock checking & inventory of chemicals required for day to day Responsible for Stability samples (Loading and unloading) under supervision. Assisting in Media preparation Preparation of solution for Plasma samples deactivation. Assisting other lab related works. Must Have Master's degree (M.Sc. or M. Pharm) in Chemistry, Pharmaceutical Sciences, Analytical Chemistry. Understanding of pharmaceutical formulation Good knowledge of written and oral communication skills for technical documentation. Time management skills to plan and executive analytical development activity.

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