Address
Form of workTo identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness.
Responsible to keep Lab and Instruments neat, clean and in working condition all the time
Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action.
To ensure the analysis activity perform in the laboratory by following approved procedures.
To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution.
Actively involve and Participate in assessment, investigations, and implementing CAPA effectively.
Responsible for Internal & External vendor follow-up and timely completion.
Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required
Perform analysis of packing materials, raw materials, stability samples, in process and finished products.
Responsible to perform and complete the work assigned by supervisor/ HOD-QC/ Head-Quality as and when required.
To receive the analysis sample includes packing materials, raw materials, In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs.
To initiate the analysis as per work allocation done by supervisor/ HOD-QC of these samples for test parameters includes description, solubility, Water content and other chemical analysis and Non-Chromatographical methods of wet laboratory section.
To execute the analysis activity by completing all necessary documentation related to instrument logbooks, analytical test report, analysis worksheets, analytical hard books and document archival after approval of samples.
To perform the wet lab instrument calibration as per the schedule and respective SOP as and when required .
To execute the chemical analysis of additional studies like stability study, method validation/ verification study/ any investigation purpose analysis.
Destruction of samples after approval and subsequent record to be updated.
To ensure the availability of valid working standards, impurity standards, reference standards and its management during usage.
To Support to maintain GC columns within the laboratory and ensure the stock availability.
Report any non-conformance i.e. Laboratory Incidence, OOS/OOT/OOC to Immediate supervisor for further action.
Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders.
PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators.
Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space.
Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment.
