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Trainee -QC

Piramalpharma

Ennore, TNPosted 2 days agoDirect from company

  • LocationEnnore, TN
  • Work typeNot stated
  • EmploymentFull-time
  • Posted29 October 2026
  • SourcePiramalpharma's careers page (Workday)
  • Last checked1 h ago on Piramalpharma's careers page
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About the role

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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 testing of In process, Intermediates and Finished products with respect to wet analysis as received on daily basis and SAP related activities.
- Strict adherence to cGMP norms and safety rules of the factory.

- Performance of daily verification activities for analytical / precision balances and KF titrator as per the defined procedure.

- Assisting the Microbiologist for water sampling activities.

- Testing of Intermediates & Finished products with respect to wet analysis.

- Receiving the FPCs of Intermediates & Finished products from all the production blocks, verification of FPC for its correctness and inwarding.

- Ensuring the cleanliness of Intermediate & Finished product samplers as per the requirement.

- Testing of Intermediates & Finished products with respect to wet analysis.

- Coordinating with QA for receipt of analytical testing protocol as and when required.

- Ensuring the contemporaneous documentation for the activities being done in IM/FP section in the corresponding log books / inward registers / check lists / analytical testing protocols / raw data sheets.

- Preparing the control samples of all the despatchable stage products and its relevant documentation.
Qualification: M.Sc. Chemistry
Experience: 0-1 Years of Lab QC Chemist

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