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
Coordinate international shipments, customs documentation, shipment tracking, and resolution of transportation issues while maintaining accurate logistics records. Manage inventory transactions, cycle counts, receipts, releases, inventory systems, and reporting in collaboration with warehouse and internal teams.
On-site · Montréal
Lead PET and SPECT radiopharmaceutical technology transfer projects from planning through implementation, managing customer relationships, scope, timelines, risks, and deliverables. Coordinate cross-functional teams and required documentation, support feasibility assessments, and ensure transfers meet FDA, cGMP, quality, budget, and schedule requirements.
On-site · Montréal
Serve as the Quality lead for technology transfer, process validation, and pre-commercialization projects, reviewing and approving related quality, validation, and manufacturing documentation. Collaborate with internal teams and external manufacturing partners to ensure regulatory compliance, assess and mitigate quality risks, support audits and regulatory inspections, and enable commercial launches.
On-site · Montréal
Lead and develop the QA Operations team, oversee quality investigations, support manufacturing operations, and maintain GMP and regulatory compliance. Represent Quality on facility expansion and capital projects, review project and validation documentation, and drive performance monitoring and continuous improvement.
On-site · Montréal
Provide regulatory guidance to cross-functional teams and prepare, review, and coordinate pharmaceutical and technical submissions for Canadian and international authorities. Maintain product compliance throughout the product lifecycle by researching requirements, reviewing documentation, and recommending changes to labeling, manufacturing, or clinical activities.
On-site · Montréal
Conduct environmental and personnel monitoring in classified areas, sample filled sterile products, and observe critical aseptic and filling operations for deficiencies. Maintain complete, traceable records, promptly report irregularities, and support troubleshooting, training, and investigations.
On-site · Montréal
Perform chemical and physical analyses on pharmaceutical products and raw materials to ensure quality and compliance. Conduct laboratory contamination monitoring and maintain accurate documentation according to GMP and GLP standards.
On-site · Montréal
The Maintenance Technical Specialist will manage and improve technical maintenance documentation and support preventive and predictive maintenance programs. They will also provide technical guidance to maintenance and operations teams to ensure equipment reliability and regulatory compliance.
On-site · Montréal
The Junior Specialist supports the deployment and maintenance of computerized systems validation, data integrity, and data governance programs. They participate in GxP system qualification, documentation, and continuous improvement initiatives to ensure regulatory compliance.
On-site · Montréal
The Project Manager is responsible for the integration, design, installation, and qualification of equipment and systems within the facility. They must manage vendors, technical personnel, project budgets, and schedules while ensuring compliance with quality and safety standards.
On-site · Montréal
The Senior Quality Technology Transfer Specialist acts as the primary quality representative for technology transfer, process validation, and pre-commercialization projects. They collaborate with multidisciplinary teams and external partners to ensure regulatory compliance, data integrity, and successful project outcomes.
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.
