JFL Lifesciences Pvt Ltd Hiring for Quality Control Chemist at Ahmedabad Full Time

• Assist in QC stability testing, prepare and maintain stability records and summaries
• Involve in training and transfer of methods to and from QC and contract manufacturers as assigned
• Modify and validate analytical procedures to meet QC’s needs
• Support design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP
• Participate in special projects and department meetings via input, feedback and execution of assigned tasks
• Execute special projects on analytical and instrument problem solving
• Conduct all quality QC chemical tests
• Perform non-radioactive and biological QC on time and record quality of product
• Adapt, maintain and operate analytical instrumentation
• Involve in procedure review and propose modifications and updates
• Ensure work environment is clean and safe complying with safety and pharmaceutical regulation
• Conduct radiation safety duties conforming to regulations
• Report monthly on supplies for QC orders involving devices and reagents
• Contribute to industrial, R&D qualification and validation activities and support routine maintenance
• Conduct various analytical testing procedures as per manufacturing/QC SOPs
• Evaluation for visual appearance, labelling, odor, taste, texture, hardness and friability.
• Moisture content: Limits are given in official compendia.

• Standards and tests of identity: designed to demonstrate clearly that the specimens examined contain the active ingredient(s) they purport to contain.

• Standards and tests of homogeneity: Apply test for uniformity of weight.

• Standards and test for purity: for potentially harmful degradation compounds that may be generated during production and storage of dosage forms and for contaminants whose presence may indicate deviation from GMP.

• Standards and assays for the active ingredient(s) and for degradation products: It provides quantitatively permitted range per tablet or capsule of average weight.

• Uniformity of content: It involves individual analysis of for a given number of dosage forms to assess possible variation. This test is particularly more important where the declared quantity of active ingredient in a single tablet is less than 5 mg and in case of sugar-coated tablets 10 mg or less.

• Standards and tests of performance: Designed to provide some assurance that the dosage form will release its active ingredient as intended. Dissolution rate tests for poorly soluble drugs, potent drugs and cases with dissolution problems; disintegration test to supplement dissolution rate tests.

• Stability indicating tests: This is to take into account the deterioration in activity or strength of the drug product that may occur because of degradation of the active ingredient in the dosage form as well as aspects of physical instability of the product e.g., development of undue color or color instability.

• Storage conditions.

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• salary depend on your interview.

Job Type: Full-time

Salary: ₹25,000.00 – ₹30,000.00 per month

Schedule:

• Day shift

Supplemental Pay:

• Overtime pay

Education:

• Bachelor’s (Preferred)

Experience:

• total work: 5 years (Preferred)

Work Remotely:

• No

Speak with the employer
+91 8511193872