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15 Synthetic Drugs Intermediates Jobs

QC Chemist

1-4 years

Vadodara

1 vacancy

QC Chemist

Synthetic Drugs Intermediates

posted 4mon ago

Job Description

We are looking for a dedicated, analytical chemist to be responsible for studying the chemical make-up of materials that are essential in our manufacturing business to ensure product safety. The chemist s responsibilities include preparing test solutions, analyzing compounds, and conducting quality control tests.
 
Expected Qualification
A Bachelor s or Master s degree in chemistry.
 
Roles and Responsibilities
To maintain the cleanliness and orderliness of Laboratory.
Responsible for sampling, Entry & analysis of all the Raw Material, In-process Material & Finished Product Material and maintain records.
Responsible for sampling, Entry & analysis of all the Packing Material and maintain records.
Responsible for sampling, Entry & analysis of by-product samples of production and maintain records.
Responsible for sampling, Entry & analysis of all the Non-moving materials and maintain records.
To label the finished materials, packing materials & Raw materials and maintain records.
To analyse the outside party sample, R&D Samples and maintain records.
To prepare and analyse marketing samples and maintain records.
To prepare and maintain records of instruments usage log books.
To prepare and standardize volumetric standard solution, Reagents and maintain its records.
To prepare the working standard, hold time / stability study samples and maintain records.
To analyse the reference / working standard and hold time / stability study samples and it records.
To prepare and maintain retain sample entry register of finished product.
To calibrate all instruments as per the Calibration plan.
To calibrate all instruments as per standard procedure and maintain records.
To prepare calibration schedule and maintain records for outside calibration of standard equipment s.
To analyse and verify the plant equipment for changeover of the equipments.
To prepare and maintain trend data and annual product quality review.
To develop the analytical methods for new products and maintain records.
To participate in investigation of deviation, change control OOT and OOS in QC activity.
To participate in Documentation and investigation of out of specification / deviation.
To prepare and maintain records of outside lab testing as per specification.
To verify the packing bags by Batch No., Qty., Mfg. date, etc.., before loading.
Any other activities as instructed by the QC Manager.
 
Skills Required
Strong problem-solving, critical thinking, and analytical skills.
Good presentation, documentation, and reporting skills.
Good verbal and written communication skills.
Strong technical skills.

Employment Type: Full Time, Permanent

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