JAMP Pharma Group is a Canadian organization headquartered in Boucherville, in the Greater Montreal area. Having experienced exceptional growth over the past 10 years, JAMP Pharma Group operates across all segments of the pharmaceutical market and now offers the widest range of generic drugs in Canada, with nearly 350 molecules. In addition to its generic division, JAMP Pharma Group operates several divisions, including Orimed, BioJAMP®, and JAMP Acute Care and Injectables, offering prescription, branded, and biosimilar products. The Group is also a leader in the over-the-counter market through its subsidiary, Groupe Wampole S.E.C., which encompasses 12 brands of natural health and cosmetic products. Since 2024, the JAMP Pharma Group has also operated its own manufacturing facility, located in Lévis. As part of JAMP Pharma, you will be able to: • Achieve your professional goals while having a significant impact on the success of the company. • Perform in a fast, agile, entrepreneurial and friendly environment. • Work with talented and multicultural professionals in order to achieve common goals. • Be part of a stable, successful and ambitious company at the forefront of innovation • Take advantage of our new, bright and welcoming offices. • Get involved socially with employees as well as the community. WANT TO MAKE HISTORY WITH US?
On-site · Boucherville
The shipping attendant is responsible for daily warehouse operations, ranging from receiving products to shipping them in a computerized environment. Key tasks include preparing orders, loading and unloading trucks, managing inventory accuracy, and coordinating with carriers.
Hybrid · Boucherville
The coordinator provides operational, administrative, and analytical support to the sales and marketing teams while assisting senior management. Key tasks include managing meeting logistics, maintaining CRM data, preparing performance reports, and coordinating promotional materials and events.
Hybrid · Lévis
The Director of Engineering and Projects is responsible for the planning, coordination, and supervision of engineering projects to ensure quality, budget, and timeline objectives are met. They will define the technical vision, manage the project portfolio, and oversee the full lifecycle of engineering projects within the organization.
On-site · Lévis
The Senior Specialist manages complex technical mandates related to the development, technology transfer, validation, and optimization of manufacturing and packaging processes. They also provide advanced technical support to production teams to resolve complex issues while ensuring compliance with GMP and regulatory standards.
On-site · Lévis
The senior project manager is responsible for planning, organizing, and coordinating R&D projects, technology transfers, and process optimization. They will also develop new formulations, supervise R&D trials, and prepare production master records.
On-site · Lévis
The specialist will lead high-complexity technical mandates related to the development, transfer, and validation of manufacturing and packaging processes. They will also provide advanced technical support to production teams to resolve complex issues while ensuring compliance with GMP and regulatory standards.
On-site · Lévis
The production operator is responsible for cleaning, adjusting, and monitoring production equipment to ensure finished products meet established standards. They also manage operational activities, maintain production cadence, and perform quality checks on semi-finished and finished goods.
On-site · Boucherville
The Sales Manager is responsible for overseeing a team of nine representatives, setting sales objectives, and managing client relationships within the Western Quebec territory. They must ensure the team's performance through regular coaching, field presence, and effective budget management.
On-site · Lévis
The technician will perform technical activities related to technology transfer, process validation, and manufacturing support in a regulated GMP environment. They will also document process trials and provide technical support for production issues.
On-site · Lévis
The medical representative is responsible for the promotion, strategic positioning, and sustainable sales growth of Orimed Pharma products among healthcare professionals. They will develop and implement a comprehensive territorial business plan to achieve annual sales objectives while maintaining strong relationships with key stakeholders.
Hybrid · Boucherville
The Business Development Director is responsible for identifying new market opportunities, developing strategic partnerships, and driving revenue growth for private label and project initiatives. They also lead commercial projects by coordinating internal teams and presenting strategic performance recommendations to management.
Hybrid · Boucherville
The sales coordinator provides administrative support to the senior director and sales team while assisting with client account management. They also coordinate promotional activities, manage business partner communications, and help organize events for the division.
On-site · Boucherville
The intern will provide first-line IT support to users and assist in managing the technological environment, including workstations and user access. They will also contribute to IT security initiatives, process improvements, and various technological projects.
On-site · Boucherville
The order picker is responsible for the daily preparation, packaging, and shipping of orders within a computerized environment. They also handle display assembly, product labeling, and cycle counts while maintaining a clean and safe workspace.
On-site · Boucherville
The specialist is responsible for the maintenance, repair, and qualification of laboratory equipment while ensuring data integrity and compliance with GMP standards. They will also manage equipment calibration, support laboratory analysts with troubleshooting, and participate in the validation of laboratory software.
On-site · Boucherville
The Instrumentation Specialist is responsible for the maintenance, repair, and qualification of laboratory equipment while ensuring data integrity and compliance with GMP standards. They will also draft qualification protocols, manage calibration schedules, and provide technical support and training to laboratory analysts.
On-site · Lévis
The maintenance and sanitation attendant is responsible for cleaning production areas, equipment, and common zones to ensure compliance with manufacturing standards. They must also perform routine cleaning tasks such as sweeping, washing surfaces, and disinfecting containers while maintaining accurate documentation.
On-site · Boucherville
The intern will participate in the issuance, revision, and implementation of specifications for commercial finished products, including drugs and natural health products. They will also communicate with partners to obtain necessary documentation and ensure the tracking of analytical methods and validation evidence.
Hybrid · Boucherville
The Product Safety Scientist is responsible for pharmacovigilance, safety surveillance, and risk management for a portfolio of pharmaceutical products. They perform medical and scientific reviews of adverse event reports and manage safety signals to ensure a favorable benefit-risk profile.
Hybrid · Boucherville
The Associate Manager provides operational and analytical support to the Patient Support Program (PSP) department in oncology and specialty products. Responsibilities include analyzing program data and KPIs, managing budgets, and coordinating with suppliers and internal sales teams.
