Find your formula for success with Jubilant Pharma Limited
Yardley, Pennsylvania
Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to our customers across geographies. We organize our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radiopharmacies), Contract Manufacturing of Sterile Injectables and Non-sterile Products and Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations and Active Pharmaceutical Ingredients.
On-site · Montréal
Lead the strategic direction of site-wide training, qualification, and workforce capability programs within a GMP pharmaceutical environment. Oversee LMS administration and ensure compliance with Health Canada, FDA, and international regulatory expectations.
On-site · Montréal
The Validation Specialist ensures the compliance of laboratory equipment and software through the execution of IQ, OQ, and PQ protocols. They are also responsible for deploying digital solutions like LIMS and managing data integrity and governance for analytical processes.
On-site · Montréal
The role provides technical oversight and support for aseptic fill-finish manufacturing operations to ensure compliant production of sterile drug products. Key duties include troubleshooting deviations, supporting technology transfers, and collaborating with Quality and Engineering teams to optimize processes.
On-site · Montréal
Oversee the operation and maintenance of utility systems, HVAC, and building automation to ensure regulatory compliance. Lead building-related projects, manage external contractors, and supervise the maintenance team's performance and training.
On-site · Montréal
The role is responsible for maintaining and improving the Environmental Monitoring program to ensure GMP compliance and a state of control in classified environments. Key duties include analyzing EM data trends, leading investigations into deviations, and implementing corrective and preventive actions (CAPA).
On-site · Montréal
The role involves performing stability analyses on radioactive end products and maintaining detailed documentation of results and observations. The student will also assist in process development and report any out-of-trend results to management for investigation.
On-site · Montréal
The student will develop annual performance review reports for equipment and identify anomalies in validation reports to drive process improvements. They will work closely with management to ensure meticulous documentation and clear communication of technical findings.
On-site · Montréal
The Stationary Machine Mechanic is responsible for the operation, troubleshooting, and maintenance of critical utility systems including boilers, cooling systems, and compressors. They must ensure all mechanical tasks comply with GMP standards and building automation requirements.
On-site · Montréal
Oversee preventive, corrective, and predictive maintenance programs while ensuring compliance with internal and regulatory GMP standards. Manage CMMS data, lead quality investigations, and contribute to the integration of new equipment and process improvements.
On-site · Montréal
The Maintenance Buyer is responsible for purchasing spare parts, tools, and services to ensure equipment and building maintenance efficiency. They manage the maintenance store inventory within the CMMS system and collaborate with managers to adhere to monthly budgets.
On-site · Montréal
Develop and execute qualification protocols for equipment, computerized systems, and manufacturing operations. Provide technical support for sterilization processes and ensure compliance with corporate standards and cGMP regulations.
On-site · Montréal
Provide Quality Assurance oversight for validation, qualification, and data integrity activities to ensure compliance with GMP and internal quality systems. Act as a quality partner to Engineering, IT, and Operations to maintain inspection-readiness and implement ALCOA+ principles.
On-site · Montréal
The role supports the implementation and maintenance of the site's Quality Risk Management framework to ensure compliance with GMP requirements. Key duties include conducting risk assessments, tracking mitigation actions, and preparing documentation for regulatory inspections.
On-site · Montréal
The Specialist, Compliance monitors and strengthens site compliance with GMP and regulatory requirements through audit readiness and regulatory surveillance. Key duties include tracking CAPAs, managing supplier quality, and preparing compliance reports for management review.
