Quality Control Officer Infocus Remedies

3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

This position is responsible for managing all Quality Control Operations of a WHO-GMP & ISO approved Tablets and Capsule manufacturing facility. Specific Responsibilities: To perform HPLC and Dissolution analysis. To review and check all Raw material, packing material, bulk and finish product specification, method of analysis and all worksheet. To review and check Different validation protocol like process, cleaning, analytical method. To review and check Stability study and hold time study protocol. To ensure for timely sampling and analysis of incoming materials, like raw materials, packing materials. To ensure for timely analysis of bulk, finish product, stability sample and validation sample. Qualifications / Requirements: Experience of performing HPLC analysis. Bachelors degree in a scientific discipline (Masters Preferred). 3-7+ years of hands-on experience in the pharmaceutical industry, with specific experience in Quality Control. Job Types: Full-time, Permanent Schedule: Day shift Yearly bonus License/Certification: FDA certification Chemical and Physio Chemical Testing. (Required) Work Location: In person,

Posted 3 days ago

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Quality Control Officer calyx pharma

2.0 - 4.0 years

2 - 3 Lacs

Boisar

Work from Office

Roles and Responsibilities Conduct quality control analysis using GC, HPLC, and other analytical methods to ensure compliance with regulatory requirements. Develop and maintain calibration protocols for laboratory instruments to ensure accuracy and precision of test results. Collaborate with cross-functional teams to resolve issues related to product quality and process optimization. Ensure adherence to cGMP guidelines and regulations in the pharmaceutical industry. Perform routine maintenance tasks on laboratory equipment to prevent downtime and ensure optimal performance. Desired Candidate Profile 2-4 years of experience in a similar role within the pharmaceutical or life sciences industry. Bachelor's degree in Chemistry (B.Sc) or Master's degree (MS/M.Sc(Science)) from a recognized university. Strong understanding of analytical method development, validation, and implementation principles. Proficiency in operating various types of chromatography systems such as GC, HPLC etc.

Posted 2 months ago

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Quality Control Professional - AMV Zuventus Healthcare Limited

5.0 - 10.0 years

2 - 6 Lacs

Sikkim

Work from Office

Job Description : Hands-on experience in -Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports operations and calibration of the instruments like HPLC, GC etc. Preferred candidate -Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV. Organisational Entity Zuventus Healthcare Ltd. Vertical ZHL Sikkim Factory Department Quality Control Continent Asia Country India Zone East Location Type S01-ZHL Factory

Posted 3 months ago

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