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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

Job Description

Key Roles/Responsibilities:

1.    Perform testing activities by following procedures and report results in timely manner of raw materials and in process samples and where assigned by the Team Leader, of bulk drug substances, final products and stability products applying cGMP and quality standards.

2.    Check and review data in compliance with Data Integrity requirement.

3.    Perform any stability study programme activities, storage of in process and final samples and retention samples management.

4.    Ensure that PPE, consumable and material are available by maintaining adequate stock control.

5.    Assist in coordination of incoming deliveries and dispatches.

6.    Arrange subcontract of QC testing and dispatches to approved suppliers as appropriate.

7.    Assist in document writing including procedure, investigation and deviation where training has been completed.

8.    Ensure that all laboratory areas and surrounding QC facilities are cleaned and maintained in accordance with housekeeping procedure and processes and remain at an inspection ready state.

9.    Ensure that all storage units, fridges, freezers and incubators are defrost and cleaned as defined per procedure and monitor and report any temperature excursion in a timely manner.

10.  Carry out general maintenance and calibration of equipment used to perform testing and inform relevant personnel in a timely manner of any failure of calibration.

11.  Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives.

12.  Maintain Quality Control information systems.

13.  Maintain a technical ability, knowledge and understanding of relevant regulatory requirements for GMP, safety and environmental policies required in order to perform role as QC Technician.

14.  Be available to provide cover for other departments within the organisation as required.

15. Be available to undertake any other duties as requested by the QC Manager in accordance with Company requirements.