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
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 specialist ensures GMP compliance by leading investigations into deviations, CAPAs, and change controls within a radiopharmaceutical environment. They are also responsible for maintaining accurate batch records and SOPs while collaborating with quality and production teams.
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 role involves managing preventive maintenance and calibration data within the CMMS and archiving technical documentation. Additionally, the student will support quality investigations, CAPA processes, and the reporting of maintenance performance indicators (KPIs).
On-site · Montréal
Assist in the development, testing, and validation of medical device software using C# and Azure DevOps. Contribute to technical documentation, Design History Files, and collaborate with multidisciplinary teams to refine software designs.
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.
On-site · Montréal
Lead strategic initiatives for new product introductions and process optimization from development through validation. Act as a process and product specialist managing the lifecycle, including CPV, PPQ, and technology transfers to sites or CMOs.
On-site · Montréal
Manage the daily schedule of sterile manufacturing while ensuring strict adherence to aseptic conduct and quality standards. Lead and motivate the production team, oversee KPI implementation, and ensure equipment maintenance and regulatory compliance.
On-site · Montréal
Manage daily sterile manufacturing schedules and ensure strict adherence to aseptic conduct principles through training and monitoring. Oversee production efficiency, manage KPIs, maintain equipment, and ensure all operations comply with cGMP and safety regulations.
On-site · Montréal
The technician is responsible for designing, maintaining, and troubleshooting specialized production equipment and systems in a regulated pharmaceutical environment. Key duties include executing calibration activities, programming PLCs, and ensuring compliance with safety and quality standards.
On-site · Montréal
Lead the strategy, governance, and continuous improvement of the Quality Management System to ensure sustainable GMP compliance. Oversee regulatory inspection readiness, CAPA programs, change control, and supplier quality management.
On-site · Montréal
Establish and manage Quality Assurance systems and teams to ensure all manufactured products meet internal and regulatory standards. Oversee change control, batch release, deviation investigations, and the site's GMP training program.
On-site · Montréal
The Supervisor, Quality Control leads laboratory activities to ensure all products are tested according to specifications and regulatory requirements. This includes planning and overseeing sample testing, coordinating tasks, and ensuring compliance with documentation standards.
On-site · Montréal
The Manager/Sr. Manager, Quality Operations is responsible for ensuring real-time quality assurance and compliance during manufacturing operations. This includes overseeing aseptic processing, documentation practices, and leading a team to uphold GMP standards.
On-site · Montréal
The Senior Specialist, SAP will configure, implement, and maintain SAP SD and MM modules to meet complex business requirements in a regulated environment. They will manage integrated business processes and ensure compliance with industry regulations.
On-site · Montréal
The Validation Manager will direct the design, planning, and execution of the site validation master plan, ensuring compliance with regulatory agencies and GMP requirements. Responsibilities include developing validation protocols, coordinating resources for validation tests, and managing a team of validation specialists.
