Piramal Pharma Solutions is a global CDMO providing comprehensive drug development and manufacturing services, specializing in APIs, clinical supplies, and innovative pharmaceutical solutions.
Lexington, KY
Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers 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 such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug product. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovator and generic companies worldwide.
On-site · Aurora
Perform laboratory testing and shift activities to support manufacturing and analytical services in compliance with quality standards. Conduct lab investigations, maintain documentation, and ensure adherence to cGMP and GLP protocols.
On-site · Aurora
Perform qualification, maintenance, and troubleshooting of analytical laboratory instrumentation to ensure operational efficiency. Maintain accurate documentation, manage equipment inventory, and assist with the installation and verification of lab systems.
On-site · Aurora
The Administrative Assistant provides comprehensive operational and executive support to the site leadership team and business functions. Responsibilities include managing visitor experiences, maintaining GMP documentation, and coordinating site activities to ensure efficient business operations.
On-site · Aurora
The S&OP Leader acts as the subject matter expert for demand and supply planning, managing the 24-month S&OP horizon and network optimization. They are responsible for coordinating cross-functional consensus, managing raw materials, and optimizing capacity utilization to drive profitability.
On-site · Aurora
Contribute to the small-scale production of active pharmaceutical ingredients and intermediates in a cGMP-compliant environment. Responsibilities include operating process equipment, performing filtrations and distillations, and maintaining detailed production documentation.
On-site · Aurora
Conduct laboratory-scale experiments for early-stage Active Pharmaceutical Ingredients and intermediates while documenting results and reporting to project leaders. Contribute to work plan definitions, develop SOPs, and potentially lead projects to meet client objectives.
On-site · Aurora
Responsible for the shipping, receiving, sampling, and storage of materials in compliance with cGMP and government regulations. Duties include managing waste, performing inventory cycle counts, and issuing batches to production.
On-site · Aurora
Lead monthly, quarterly, and annual financial close processes while ensuring accurate IFRS reporting and balance sheet reconciliations. Oversee tax compliance, manufacturing accounting, and coordinate external audits to maintain strong financial controls.
