Job Description

Roles and Responsibilities :-

• Preparing specifications for all raw materials, packing materials, finished products, intermediates and solvents, and reagents used in analyses.
• Inspecting, sampling, and testing of all starting materials including packaging materials, intermediate and finished products as per procedures defined in the Standard Operating Procedures
• Performing stability testing to assess product stability.
• Monitoring environmental conditions are met as per current Good Manufacturing Practices (cGMP) requirements.
• Preparing analysis reports for the tested samples, and recording and investigating any results that are Out Of Specifications (OOS).
• Approving product batches for sale after ensuring it meets quality, safety and efficacy standards prescribed.
• Calibration of all laboratory instruments and devices used in the testing.
• Validation of analytical methods used in the testing.
• Retaining reference samples from each batch of products released to the market.
• Reviewing the batch manufacturing and packing records and assessing the test reports to ensure products are of the desired quality and have been properly packed and labeled.
• . Participating in any investigation that follows market complaints about the quality of a product.

Qualification :-

• Pharma and Pharmaceutical experience required.
• Graduation with Pharma
• Minimum 3 Years of Exp. required.
• Only male candidates can apply
• Candidates from Indore will get preference.

Job Type: Full-time Salary: \xe2\x82\xb925,000.00 - \xe2\x82\xb960,000.00 per month Benefits:

• Health insurance
• Provident Fund

Experience:

• Quality control: 3 years (Required)

Ability to Commute:

• Lasudiya Mori, Indore, Madhya Pradesh (Required)

Ability to Relocate:

• Lasudiya Mori, Indore, Madhya Pradesh: Relocate before starting work (Required)

Work Location: In person Speak with the employer
+91 9303781289