Trainee - QC

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Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing  organization (CDMO), offering end-to-end development and manufacturing  solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.  

This enables us to offer a comprehensive range of services including Drug Discovery  Solutions, Process & Pharmaceutical Development services, Clinical Trial  Supplies, Commercial supply of APIs and Finished dosage forms. We also offer  specialized services like development and manufacture of Highly Potent APIs  and Antibody Drug Conjugation.  

Our capability as an integrated service provider  & experience with various technologies enables us to serve Innovator and  Generic companies worldwide.  

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Trainee - QC

Job Description

Responsible for sampling, testing and clearance of all the materials (Raw materials, In Process Samples, Intermediates, Finished Products and Stability Samples) as received in wet lab section.

Responsibilities:

• Strict adherence to cGMP norms and safety rules of the factory.
• Testing of raw materials, in process, intermediates, finished products and stability samples with respect to wet analysis, accurately without any deviations and delays.
• Calibration of Analytical balances, pH meter, KF titrator, Auto titrator, Melting point apparatus, UV and FTIR instruments as per the calibration schedules without delays.
• Planning of wet analysis to release the results right time as per the requirement.
• Reviewing of the analytical data and releasing the results right time to meet the dispatch requirements as per the planned scheduled.
• Coordinating within the department in clearing the analytical results as per the production plans.
• Coordinating with Quality Assurance department in releasing the products.
• Daily planning of wet analysis as per the dispatch and production priority
• Trouble shooting of related instruments to avoid break downs.
• Testing of wet analysis without any deviations following the procedures.
• Fill up the protocols on line and maintain raw data.
• All records and documents should be maintain as per SOP.
• Maintaining laboratory systems as per the regulatory requirements.
• Preparation and standardization of volumetric solution and reagent solution as per the requirement.

Analytical Balance, cGMP Regulations